Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Neurodevelopmental abnormality (HP:0012759)

Parent Node:
Neurodevelopmental delay (HP:0012758)

..Starting node
..Motor delay (HP:0001270)

Term ID:

1270

Name:

Motor delay

Synonym:

Delay in motor development; Delayed early motor milestones; Delayed motor development; Delayed motor milestones; Locomotor delay; Motor developmental delay; Motor developmental milestones not achieved; Motor retardation; No development of motor milestones; Retarded motor development

Definition:

A type of Developmental delay characterized by a delay in acquiring motor skills.

Comments:

Reference:

HP:0001270

Genes and Diseases:

Child Nodes:

........

Delayed gross motor development (HP:0002194)

................... HP:0025335 Delayed ability to stand
................... HP:0025336 Delayed ability to sit

........

Delayed fine motor development (HP:0010862)

Sister Nodes:

Delayed social development (HP:0012434)

Delayed speech and language development (HP:0000750)

Global developmental delay (HP:0001263)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	DiseaseId	DiseaseName	DiseaseMIM	ConceptID	Source	Typical association	ClinVar variants	HGNC ID	GeneMIM
HPO disease - gene - phenotype typical associations:
HP:0001270	HP:0001270	Motor delay	0	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0001270	Motor delay	0	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0001270	Motor delay	0	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0001270	Motor delay	0	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0001270	Motor delay	0	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0001270	Motor delay	0	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0001270	Motor delay	0	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0001270	Motor delay	0	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0001270	Motor delay	0	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0001270	Motor delay	0	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0001270	Motor delay	0	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0001270	Motor delay	0	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0001270	Motor delay	0	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0001270	Motor delay	0	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0001270	Motor delay	0	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0001270	Motor delay	0	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0001270	Motor delay	0	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0001270	Motor delay	0	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0001270	Motor delay	0	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0001270	Motor delay	0	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0001270	Motor delay	0	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0001270	Motor delay	0	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0001270	Motor delay	0	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0001270	Motor delay	0	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0001270	Motor delay	0	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0001270	Motor delay	0	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0001270	Motor delay	0	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0001270	Motor delay	0	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0001270	Motor delay	0	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0001270	Motor delay	0	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0001270	Motor delay	0	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0001270	Motor delay	0	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0001270	Motor delay	0	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0001270	Motor delay	0	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0001270	Motor delay	0	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0001270	Motor delay	0	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0001270	Motor delay	0	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0001270	Motor delay	0	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0001270	Motor delay	0	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0001270	Motor delay	0	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0001270	Motor delay	0	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0001270	Motor delay	0	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0001270	Motor delay	0	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0001270	Motor delay	0	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0001270	Motor delay	0	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0001270	Motor delay	0	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0001270	Motor delay	0	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0001270	Motor delay	0	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0001270	Motor delay	0	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0001270	Motor delay	0	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0001270	Motor delay	0	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0001270	Motor delay	0	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0001270	Motor delay	0	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0001270	Motor delay	0	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0001270	Motor delay	0	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0001270	Motor delay	0	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0001270	Motor delay	0	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0001270	Motor delay	0	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0001270	Motor delay	0	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0001270	Motor delay	0	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0001270	Motor delay	0	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0001270	Motor delay	0	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0001270	Motor delay	0	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0001270	Motor delay	0	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0001270	Motor delay	0	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0001270	Motor delay	0	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0001270	Motor delay	0	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0001270	Motor delay	0	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0001270	Motor delay	0	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0001270	Motor delay	0	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0001270	Motor delay	0	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0001270	Motor delay	0	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0001270	Motor delay	0	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0001270	Motor delay	0	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0001270	Motor delay	0	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0001270	Motor delay	0	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0001270	Motor delay	0	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0001270	Motor delay	0	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0001270	Motor delay	0	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0001270	Motor delay	0	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0001270	Motor delay	0	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0001270	Motor delay	0	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0001270	Motor delay	0	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0001270	Motor delay	0	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0001270	Motor delay	0	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0001270	Motor delay	0	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0001270	Motor delay	0	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0001270	Motor delay	0	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0001270	Motor delay	0	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0001270	Motor delay	0	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0001270	Motor delay	0	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0001270	Motor delay	0	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0001270	Motor delay	0	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0001270	Motor delay	0	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0001270	Motor delay	0	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0001270	Motor delay	0	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0001270	Motor delay	0	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0001270	Motor delay	0	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0001270	Motor delay	0	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0001270	Motor delay	0	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0001270	Motor delay	0	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0001270	Motor delay	0	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0001270	Motor delay	0	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0001270	Motor delay	0	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0001270	Motor delay	0	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0001270	Motor delay	0	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0001270	Motor delay	0	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0001270	Motor delay	0	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0001270	Motor delay	0	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0001270	Motor delay	0	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0001270	Motor delay	0	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0001270	Motor delay	0	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0001270	Motor delay	0	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0001270	Motor delay	0	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0001270	Motor delay	0	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0001270	Motor delay	0	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0001270	Motor delay	0	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0001270	Motor delay	0	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0001270	Motor delay	0	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0001270	Motor delay	0	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0001270	Motor delay	0	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0001270	Motor delay	0	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0001270	Motor delay	0	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0001270	Motor delay	0	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0001270	Motor delay	0	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0001270	Motor delay	0	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0001270	Motor delay	0	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0001270	Motor delay	0	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0001270	Motor delay	0	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0001270	Motor delay	0	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0001270	Motor delay	0	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0001270	Motor delay	0	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0001270	Motor delay	0	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0001270	Motor delay	0	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0001270	Motor delay	0	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0001270	Motor delay	0	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0001270	Motor delay	0	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0001270	Motor delay	0	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0001270	Motor delay	0	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0001270	Motor delay	0	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0001270	Motor delay	0	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0001270	Motor delay	0	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0001270	Motor delay	0	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0001270	Motor delay	0	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0001270	Motor delay	0	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0001270	Motor delay	0	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0001270	Motor delay	0	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0001270	Motor delay	0	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0001270	Motor delay	0	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0001270	Motor delay	0	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0001270	Motor delay	0	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0001270	Motor delay	0	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0001270	Motor delay	0	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0001270	Motor delay	0	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0001270	Motor delay	0	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0001270	Motor delay	0	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0001270	Motor delay	0	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0001270	Motor delay	0	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0001270	Motor delay	0	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0001270	Motor delay	0	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0001270	Motor delay	0	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0001270	Motor delay	0	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0001270	Motor delay	0	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0001270	Motor delay	0	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0001270	Motor delay	0	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0001270	Motor delay	0	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0001270	Motor delay	0	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0001270	Motor delay	0	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0001270	Motor delay	0	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0001270	Motor delay	0	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0001270	Motor delay	0	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0001270	Motor delay	0	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0001270	Motor delay	0	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0001270	Motor delay	0	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0001270	Motor delay	0	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0001270	Motor delay	0	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0001270	Motor delay	0	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0001270	Motor delay	0	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0001270	Motor delay	0	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0001270	Motor delay	0	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0001270	Motor delay	0	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0001270	Motor delay	0	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0001270	Motor delay	0	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0001270	Motor delay	0	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0001270	Motor delay	0	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0001270	Motor delay	0	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0001270	Motor delay	0	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0001270	Motor delay	0	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0001270	Motor delay	0	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0001270	Motor delay	0	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0001270	Motor delay	0	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0001270	Motor delay	0	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0001270	Motor delay	0	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0001270	Motor delay	0	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0001270	Motor delay	0	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0001270	Motor delay	0	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0001270	Motor delay	0	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0001270	Motor delay	0	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0001270	Motor delay	0	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0001270	Motor delay	0	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0001270	Motor delay	0	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0001270	Motor delay	0	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0001270	Motor delay	0	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0001270	Motor delay	0	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0001270	Motor delay	0	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0001270	Motor delay	0	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0001270	Motor delay	0	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0001270	Motor delay	0	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0001270	Motor delay	0	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0001270	Motor delay	0	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0001270	Motor delay	0	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0001270	Motor delay	0	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0001270	Motor delay	0	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0001270	Motor delay	0	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0001270	Motor delay	0	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0001270	Motor delay	0	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0001270	Motor delay	0	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0001270	Motor delay	0	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0001270	Motor delay	0	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0001270	Motor delay	0	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0001270	Motor delay	0	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0001270	Motor delay	0	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0001270	Motor delay	0	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0001270	Motor delay	0	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0001270	Motor delay	0	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0001270	Motor delay	0	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0001270	Motor delay	0	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0001270	Motor delay	0	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0001270	Motor delay	0	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0001270	Motor delay	0	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0001270	Motor delay	0	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0001270	Motor delay	0	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0001270	Motor delay	0	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0001270	Motor delay	0	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0001270	Motor delay	0	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0001270	Motor delay	0	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0001270	Motor delay	0	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0001270	Motor delay	0	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0001270	Motor delay	0	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0001270	Motor delay	0	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0001270	Motor delay	0	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0001270	Motor delay	0	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0001270	Motor delay	0	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0001270	Motor delay	0	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0001270	Motor delay	0	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0001270	Motor delay	0	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0001270	Motor delay	0	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0001270	Motor delay	0	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0001270	Motor delay	0	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0001270	Motor delay	0	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0001270	Motor delay	0	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0001270	Motor delay	0	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0001270	Motor delay	0	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0001270	Motor delay	0	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0001270	Motor delay	0	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0001270	Motor delay	0	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0001270	Motor delay	0	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0001270	Motor delay	0	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0001270	Motor delay	0	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0001270	Motor delay	0	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0001270	Motor delay	0	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0001270	Motor delay	0	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0001270	Motor delay	0	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0001270	Motor delay	0	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0001270	Motor delay	0	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0001270	Motor delay	0	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0001270	Motor delay	0	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0001270	Motor delay	0	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0001270	Motor delay	0	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0001270	Motor delay	0	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0001270	Motor delay	0	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0001270	Motor delay	0	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0001270	Motor delay	0	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0001270	Motor delay	0	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0001270	Motor delay	0	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0001270	Motor delay	0	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0001270	Motor delay	0	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0001270	Motor delay	0	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0001270	Motor delay	0	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0001270	Motor delay	0	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0001270	Motor delay	0	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0001270	Motor delay	0	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0001270	Motor delay	0	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0001270	Motor delay	0	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0001270	Motor delay	0	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0001270	Motor delay	0	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0001270	Motor delay	0	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0001270	Motor delay	0	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0001270	Motor delay	0	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0001270	Motor delay	0	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0001270	Motor delay	0	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0001270	Motor delay	0	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0001270	Motor delay	0	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0001270	Motor delay	0	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0001270	Motor delay	0	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0001270	Motor delay	0	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0001270	Motor delay	0	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0001270	Motor delay	0	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0001270	Motor delay	0	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0001270	Motor delay	0	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0001270	Motor delay	0	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0001270	Motor delay	0	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0001270	Motor delay	0	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0001270	Motor delay	0	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0001270	Motor delay	0	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0001270	Motor delay	0	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0001270	Motor delay	0	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0001270	Motor delay	0	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0001270	Motor delay	0	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0001270	Motor delay	0	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0001270	Motor delay	0	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0001270	Motor delay	0	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0001270	Motor delay	0	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0001270	Motor delay	0	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0001270	Motor delay	0	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0001270	Motor delay	0	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0001270	Motor delay	0	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0001270	Motor delay	0	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0001270	Motor delay	0	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0001270	Motor delay	0	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0001270	Motor delay	0	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0001270	Motor delay	0	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0001270	Motor delay	0	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0001270	Motor delay	0	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0001270	Motor delay	0	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0001270	Motor delay	0	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0001270	Motor delay	0	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0001270	Motor delay	0	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0001270	Motor delay	0	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0001270	Motor delay	0	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0001270	Motor delay	0	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0001270	Motor delay	0	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0001270	Motor delay	0	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0001270	Motor delay	0	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0001270	Motor delay	0	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0001270	Motor delay	0	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0001270	Motor delay	0	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0001270	Motor delay	0	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0001270	Motor delay	0	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0001270	Motor delay	0	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0001270	Motor delay	0	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0001270	Motor delay	0	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0001270	Motor delay	0	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0001270	Motor delay	0	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0001270	Motor delay	0	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0001270	Motor delay	0	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0001270	Motor delay	0	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0001270	Motor delay	0	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0001270	Motor delay	0	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0001270	Motor delay	0	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0001270	Motor delay	0	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0001270	Motor delay	0	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0001270	Motor delay	0	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0002194	Delayed gross motor development	1	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0002194	Delayed gross motor development	1	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0010862	Delayed fine motor development	1	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0032988	Persistent head lag	1	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0032988	Persistent head lag	1	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0010862	Delayed fine motor development	1	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0002194	Delayed gross motor development	1	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0010862	Delayed fine motor development	1	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0032988	Persistent head lag	1	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0010862	Delayed fine motor development	1	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0032988	Persistent head lag	1	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0002194	Delayed gross motor development	1	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0032988	Persistent head lag	1	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0010862	Delayed fine motor development	1	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0032988	Persistent head lag	1	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0002194	Delayed gross motor development	1	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0032988	Persistent head lag	1	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0010862	Delayed fine motor development	1	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0002194	Delayed gross motor development	1	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0002194	Delayed gross motor development	1	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0002194	Delayed gross motor development	1	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0010862	Delayed fine motor development	1	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0010862	Delayed fine motor development	1	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0032988	Persistent head lag	1	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0032988	Persistent head lag	1	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0010862	Delayed fine motor development	1	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0002194	Delayed gross motor development	1	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0002194	Delayed gross motor development	1	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0010862	Delayed fine motor development	1	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0032988	Persistent head lag	1	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0002194	Delayed gross motor development	1	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0010862	Delayed fine motor development	1	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0032988	Persistent head lag	1	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0002194	Delayed gross motor development	1	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0010862	Delayed fine motor development	1	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0032988	Persistent head lag	1	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0002194	Delayed gross motor development	1	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0032988	Persistent head lag	1	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0010862	Delayed fine motor development	1	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0002194	Delayed gross motor development	1	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0010862	Delayed fine motor development	1	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0032988	Persistent head lag	1	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0002194	Delayed gross motor development	1	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0010862	Delayed fine motor development	1	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0032988	Persistent head lag	1	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0002194	Delayed gross motor development	1	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0010862	Delayed fine motor development	1	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0032988	Persistent head lag	1	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0002194	Delayed gross motor development	1	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0032988	Persistent head lag	1	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0010862	Delayed fine motor development	1	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0010862	Delayed fine motor development	1	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0032988	Persistent head lag	1	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0002194	Delayed gross motor development	1	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0002194	Delayed gross motor development	1	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0032988	Persistent head lag	1	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0010862	Delayed fine motor development	1	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0002194	Delayed gross motor development	1	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0010862	Delayed fine motor development	1	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0032988	Persistent head lag	1	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0032988	Persistent head lag	1	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0010862	Delayed fine motor development	1	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0002194	Delayed gross motor development	1	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0010862	Delayed fine motor development	1	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0032988	Persistent head lag	1	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0002194	Delayed gross motor development	1	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0002194	Delayed gross motor development	1	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0032988	Persistent head lag	1	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0010862	Delayed fine motor development	1	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0002194	Delayed gross motor development	1	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0010862	Delayed fine motor development	1	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0032988	Persistent head lag	1	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0002194	Delayed gross motor development	1	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0032988	Persistent head lag	1	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0010862	Delayed fine motor development	1	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0032988	Persistent head lag	1	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0010862	Delayed fine motor development	1	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0002194	Delayed gross motor development	1	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0032988	Persistent head lag	1	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0010862	Delayed fine motor development	1	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0002194	Delayed gross motor development	1	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0010862	Delayed fine motor development	1	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0032988	Persistent head lag	1	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0002194	Delayed gross motor development	1	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0032988	Persistent head lag	1	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0032988	Persistent head lag	1	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0032988	Persistent head lag	1	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0032988	Persistent head lag	1	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0032988	Persistent head lag	1	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0032988	Persistent head lag	1	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0032988	Persistent head lag	1	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0032988	Persistent head lag	1	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0010862	Delayed fine motor development	1	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0032988	Persistent head lag	1	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0002194	Delayed gross motor development	1	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0002194	Delayed gross motor development	1	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0032988	Persistent head lag	1	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0010862	Delayed fine motor development	1	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0010862	Delayed fine motor development	1	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0032988	Persistent head lag	1	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0002194	Delayed gross motor development	1	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0002194	Delayed gross motor development	1	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0010862	Delayed fine motor development	1	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0032988	Persistent head lag	1	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0002194	Delayed gross motor development	1	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0032988	Persistent head lag	1	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0010862	Delayed fine motor development	1	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0002194	Delayed gross motor development	1	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0032988	Persistent head lag	1	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0010862	Delayed fine motor development	1	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0010862	Delayed fine motor development	1	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0032988	Persistent head lag	1	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0002194	Delayed gross motor development	1	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0002194	Delayed gross motor development	1	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0010862	Delayed fine motor development	1	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0032988	Persistent head lag	1	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0002194	Delayed gross motor development	1	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0010862	Delayed fine motor development	1	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0032988	Persistent head lag	1	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0002194	Delayed gross motor development	1	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0010862	Delayed fine motor development	1	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0032988	Persistent head lag	1	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0002194	Delayed gross motor development	1	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0032988	Persistent head lag	1	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0010862	Delayed fine motor development	1	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0002194	Delayed gross motor development	1	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0010862	Delayed fine motor development	1	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0032988	Persistent head lag	1	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0002194	Delayed gross motor development	1	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0010862	Delayed fine motor development	1	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0032988	Persistent head lag	1	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0032988	Persistent head lag	1	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0010862	Delayed fine motor development	1	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0002194	Delayed gross motor development	1	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0002194	Delayed gross motor development	1	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0010862	Delayed fine motor development	1	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0032988	Persistent head lag	1	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0002194	Delayed gross motor development	1	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0010862	Delayed fine motor development	1	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0032988	Persistent head lag	1	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0002194	Delayed gross motor development	1	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0010862	Delayed fine motor development	1	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0032988	Persistent head lag	1	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0002194	Delayed gross motor development	1	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0010862	Delayed fine motor development	1	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0032988	Persistent head lag	1	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0002194	Delayed gross motor development	1	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0010862	Delayed fine motor development	1	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0032988	Persistent head lag	1	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0010862	Delayed fine motor development	1	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0032988	Persistent head lag	1	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0002194	Delayed gross motor development	1	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0002194	Delayed gross motor development	1	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0032988	Persistent head lag	1	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0010862	Delayed fine motor development	1	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0010862	Delayed fine motor development	1	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0032988	Persistent head lag	1	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0002194	Delayed gross motor development	1	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0002194	Delayed gross motor development	1	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0032988	Persistent head lag	1	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0010862	Delayed fine motor development	1	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0032988	Persistent head lag	1	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0010862	Delayed fine motor development	1	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0002194	Delayed gross motor development	1	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0032988	Persistent head lag	1	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0010862	Delayed fine motor development	1	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0002194	Delayed gross motor development	1	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0002194	Delayed gross motor development	1	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0032988	Persistent head lag	1	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0010862	Delayed fine motor development	1	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0002194	Delayed gross motor development	1	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0010862	Delayed fine motor development	1	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0032988	Persistent head lag	1	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0010862	Delayed fine motor development	1	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0032988	Persistent head lag	1	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0002194	Delayed gross motor development	1	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0032988	Persistent head lag	1	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0010862	Delayed fine motor development	1	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0002194	Delayed gross motor development	1	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0002194	Delayed gross motor development	1	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0010862	Delayed fine motor development	1	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0032988	Persistent head lag	1	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0002194	Delayed gross motor development	1	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0032988	Persistent head lag	1	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0010862	Delayed fine motor development	1	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0002194	Delayed gross motor development	1	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0010862	Delayed fine motor development	1	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0032988	Persistent head lag	1	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0002194	Delayed gross motor development	1	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0032988	Persistent head lag	1	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0010862	Delayed fine motor development	1	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0010862	Delayed fine motor development	1	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0032988	Persistent head lag	1	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0002194	Delayed gross motor development	1	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0002194	Delayed gross motor development	1	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0032988	Persistent head lag	1	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0010862	Delayed fine motor development	1	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0010862	Delayed fine motor development	1	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0032988	Persistent head lag	1	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0002194	Delayed gross motor development	1	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0002194	Delayed gross motor development	1	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0032988	Persistent head lag	1	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0010862	Delayed fine motor development	1	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0032988	Persistent head lag	1	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0010862	Delayed fine motor development	1	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0002194	Delayed gross motor development	1	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0002194	Delayed gross motor development	1	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0010862	Delayed fine motor development	1	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0032988	Persistent head lag	1	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0002194	Delayed gross motor development	1	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0032988	Persistent head lag	1	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0010862	Delayed fine motor development	1	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0002194	Delayed gross motor development	1	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0010862	Delayed fine motor development	1	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0032988	Persistent head lag	1	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0002194	Delayed gross motor development	1	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0032988	Persistent head lag	1	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0010862	Delayed fine motor development	1	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0002194	Delayed gross motor development	1	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0032988	Persistent head lag	1	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0010862	Delayed fine motor development	1	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0010862	Delayed fine motor development	1	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0032988	Persistent head lag	1	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0002194	Delayed gross motor development	1	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0002194	Delayed gross motor development	1	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0010862	Delayed fine motor development	1	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0032988	Persistent head lag	1	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0002194	Delayed gross motor development	1	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0010862	Delayed fine motor development	1	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0032988	Persistent head lag	1	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0002194	Delayed gross motor development	1	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0010862	Delayed fine motor development	1	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0032988	Persistent head lag	1	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0002194	Delayed gross motor development	1	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0010862	Delayed fine motor development	1	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0032988	Persistent head lag	1	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0002194	Delayed gross motor development	1	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0032988	Persistent head lag	1	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0010862	Delayed fine motor development	1	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0002194	Delayed gross motor development	1	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0010862	Delayed fine motor development	1	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0032988	Persistent head lag	1	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0002194	Delayed gross motor development	1	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0010862	Delayed fine motor development	1	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0032988	Persistent head lag	1	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0002194	Delayed gross motor development	1	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0010862	Delayed fine motor development	1	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0032988	Persistent head lag	1	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0002194	Delayed gross motor development	1	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0010862	Delayed fine motor development	1	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0032988	Persistent head lag	1	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0002194	Delayed gross motor development	1	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0010862	Delayed fine motor development	1	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0032988	Persistent head lag	1	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0002194	Delayed gross motor development	1	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0010862	Delayed fine motor development	1	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0032988	Persistent head lag	1	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0032988	Persistent head lag	1	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0010862	Delayed fine motor development	1	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0002194	Delayed gross motor development	1	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0002194	Delayed gross motor development	1	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0032988	Persistent head lag	1	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0010862	Delayed fine motor development	1	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0002194	Delayed gross motor development	1	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0032988	Persistent head lag	1	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0010862	Delayed fine motor development	1	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0010862	Delayed fine motor development	1	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0032988	Persistent head lag	1	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0002194	Delayed gross motor development	1	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0010862	Delayed fine motor development	1	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0032988	Persistent head lag	1	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0002194	Delayed gross motor development	1	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0002194	Delayed gross motor development	1	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0010862	Delayed fine motor development	1	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0032988	Persistent head lag	1	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0010862	Delayed fine motor development	1	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0032988	Persistent head lag	1	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0002194	Delayed gross motor development	1	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0010862	Delayed fine motor development	1	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0032988	Persistent head lag	1	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0002194	Delayed gross motor development	1	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0010862	Delayed fine motor development	1	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0032988	Persistent head lag	1	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0002194	Delayed gross motor development	1	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0010862	Delayed fine motor development	1	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0032988	Persistent head lag	1	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0002194	Delayed gross motor development	1	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0010862	Delayed fine motor development	1	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0032988	Persistent head lag	1	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0002194	Delayed gross motor development	1	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0032988	Persistent head lag	1	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0010862	Delayed fine motor development	1	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0002194	Delayed gross motor development	1	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0002194	Delayed gross motor development	1	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0010862	Delayed fine motor development	1	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0032988	Persistent head lag	1	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0002194	Delayed gross motor development	1	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0010862	Delayed fine motor development	1	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0032988	Persistent head lag	1	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0032988	Persistent head lag	1	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0010862	Delayed fine motor development	1	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0002194	Delayed gross motor development	1	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0032988	Persistent head lag	1	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0010862	Delayed fine motor development	1	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0002194	Delayed gross motor development	1	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0010862	Delayed fine motor development	1	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0032988	Persistent head lag	1	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0002194	Delayed gross motor development	1	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0002194	Delayed gross motor development	1	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0032988	Persistent head lag	1	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0010862	Delayed fine motor development	1	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0002194	Delayed gross motor development	1	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0032988	Persistent head lag	1	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0010862	Delayed fine motor development	1	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0032988	Persistent head lag	1	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0010862	Delayed fine motor development	1	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0002194	Delayed gross motor development	1	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0002194	Delayed gross motor development	1	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0010862	Delayed fine motor development	1	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0032988	Persistent head lag	1	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0002194	Delayed gross motor development	1	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0010862	Delayed fine motor development	1	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0032988	Persistent head lag	1	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0002194	Delayed gross motor development	1	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0010862	Delayed fine motor development	1	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0032988	Persistent head lag	1	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0002194	Delayed gross motor development	1	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0010862	Delayed fine motor development	1	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0032988	Persistent head lag	1	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0010862	Delayed fine motor development	1	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0032988	Persistent head lag	1	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0002194	Delayed gross motor development	1	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0032988	Persistent head lag	1	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0010862	Delayed fine motor development	1	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0002194	Delayed gross motor development	1	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0032988	Persistent head lag	1	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0010862	Delayed fine motor development	1	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0002194	Delayed gross motor development	1	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0032988	Persistent head lag	1	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0010862	Delayed fine motor development	1	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0002194	Delayed gross motor development	1	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0002194	Delayed gross motor development	1	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0010862	Delayed fine motor development	1	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0032988	Persistent head lag	1	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0032988	Persistent head lag	1	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0010862	Delayed fine motor development	1	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0002194	Delayed gross motor development	1	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0002194	Delayed gross motor development	1	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0032988	Persistent head lag	1	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0010862	Delayed fine motor development	1	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0002194	Delayed gross motor development	1	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0032988	Persistent head lag	1	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0010862	Delayed fine motor development	1	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0002194	Delayed gross motor development	1	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0032988	Persistent head lag	1	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0010862	Delayed fine motor development	1	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0002194	Delayed gross motor development	1	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0010862	Delayed fine motor development	1	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0032988	Persistent head lag	1	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0002194	Delayed gross motor development	1	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0032988	Persistent head lag	1	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0010862	Delayed fine motor development	1	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0002194	Delayed gross motor development	1	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0010862	Delayed fine motor development	1	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0032988	Persistent head lag	1	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0032988	Persistent head lag	1	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0010862	Delayed fine motor development	1	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0002194	Delayed gross motor development	1	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0002194	Delayed gross motor development	1	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0010862	Delayed fine motor development	1	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0032988	Persistent head lag	1	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0010862	Delayed fine motor development	1	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0032988	Persistent head lag	1	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0002194	Delayed gross motor development	1	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0002194	Delayed gross motor development	1	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0010862	Delayed fine motor development	1	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0032988	Persistent head lag	1	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0002194	Delayed gross motor development	1	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0032988	Persistent head lag	1	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0010862	Delayed fine motor development	1	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0002194	Delayed gross motor development	1	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0010862	Delayed fine motor development	1	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0032988	Persistent head lag	1	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0002194	Delayed gross motor development	1	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0010862	Delayed fine motor development	1	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0032988	Persistent head lag	1	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0002194	Delayed gross motor development	1	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0032988	Persistent head lag	1	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0010862	Delayed fine motor development	1	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0002194	Delayed gross motor development	1	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0010862	Delayed fine motor development	1	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0032988	Persistent head lag	1	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0032988	Persistent head lag	1	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0010862	Delayed fine motor development	1	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0002194	Delayed gross motor development	1	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0010862	Delayed fine motor development	1	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0032988	Persistent head lag	1	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0002194	Delayed gross motor development	1	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0002194	Delayed gross motor development	1	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0010862	Delayed fine motor development	1	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0032988	Persistent head lag	1	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0002194	Delayed gross motor development	1	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0032988	Persistent head lag	1	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0010862	Delayed fine motor development	1	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0002194	Delayed gross motor development	1	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0032988	Persistent head lag	1	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0010862	Delayed fine motor development	1	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0002194	Delayed gross motor development	1	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0010862	Delayed fine motor development	1	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0032988	Persistent head lag	1	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0010862	Delayed fine motor development	1	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0032988	Persistent head lag	1	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0002194	Delayed gross motor development	1	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0010862	Delayed fine motor development	1	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0032988	Persistent head lag	1	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0002194	Delayed gross motor development	1	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0010862	Delayed fine motor development	1	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0032988	Persistent head lag	1	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0002194	Delayed gross motor development	1	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0002194	Delayed gross motor development	1	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0032988	Persistent head lag	1	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0010862	Delayed fine motor development	1	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0002194	Delayed gross motor development	1	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0010862	Delayed fine motor development	1	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0032988	Persistent head lag	1	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0010862	Delayed fine motor development	1	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0032988	Persistent head lag	1	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0002194	Delayed gross motor development	1	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0002194	Delayed gross motor development	1	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0010862	Delayed fine motor development	1	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0032988	Persistent head lag	1	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0002194	Delayed gross motor development	1	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0032988	Persistent head lag	1	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0010862	Delayed fine motor development	1	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0032988	Persistent head lag	1	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0032988	Persistent head lag	1	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0032988	Persistent head lag	1	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0032988	Persistent head lag	1	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0032988	Persistent head lag	1	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0032988	Persistent head lag	1	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0002194	Delayed gross motor development	1	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0032988	Persistent head lag	1	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0010862	Delayed fine motor development	1	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0002194	Delayed gross motor development	1	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0032988	Persistent head lag	1	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0010862	Delayed fine motor development	1	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0002194	Delayed gross motor development	1	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0032988	Persistent head lag	1	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0010862	Delayed fine motor development	1	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0002194	Delayed gross motor development	1	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0010862	Delayed fine motor development	1	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0032988	Persistent head lag	1	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0010862	Delayed fine motor development	1	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0032988	Persistent head lag	1	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0002194	Delayed gross motor development	1	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0002194	Delayed gross motor development	1	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0032988	Persistent head lag	1	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0032988	Persistent head lag	1	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0010862	Delayed fine motor development	1	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0010862	Delayed fine motor development	1	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0002194	Delayed gross motor development	1	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0010862	Delayed fine motor development	1	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0032988	Persistent head lag	1	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0002194	Delayed gross motor development	1	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0010862	Delayed fine motor development	1	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0032988	Persistent head lag	1	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0002194	Delayed gross motor development	1	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0010862	Delayed fine motor development	1	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0032988	Persistent head lag	1	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0002194	Delayed gross motor development	1	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0002194	Delayed gross motor development	1	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0032988	Persistent head lag	1	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0010862	Delayed fine motor development	1	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0002194	Delayed gross motor development	1	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0010862	Delayed fine motor development	1	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0032988	Persistent head lag	1	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0002194	Delayed gross motor development	1	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0010862	Delayed fine motor development	1	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0032988	Persistent head lag	1	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0002194	Delayed gross motor development	1	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0010862	Delayed fine motor development	1	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0032988	Persistent head lag	1	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0010862	Delayed fine motor development	1	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0032988	Persistent head lag	1	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0002194	Delayed gross motor development	1	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0002194	Delayed gross motor development	1	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0010862	Delayed fine motor development	1	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0032988	Persistent head lag	1	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0002194	Delayed gross motor development	1	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0032988	Persistent head lag	1	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0010862	Delayed fine motor development	1	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0002194	Delayed gross motor development	1	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0010862	Delayed fine motor development	1	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0032988	Persistent head lag	1	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0002194	Delayed gross motor development	1	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0010862	Delayed fine motor development	1	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0032988	Persistent head lag	1	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0002194	Delayed gross motor development	1	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0010862	Delayed fine motor development	1	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0032988	Persistent head lag	1	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0002194	Delayed gross motor development	1	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0032988	Persistent head lag	1	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0010862	Delayed fine motor development	1	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0002194	Delayed gross motor development	1	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0010862	Delayed fine motor development	1	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0032988	Persistent head lag	1	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0002194	Delayed gross motor development	1	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0032988	Persistent head lag	1	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0010862	Delayed fine motor development	1	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0002194	Delayed gross motor development	1	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0032988	Persistent head lag	1	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0010862	Delayed fine motor development	1	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0002194	Delayed gross motor development	1	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0032988	Persistent head lag	1	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0010862	Delayed fine motor development	1	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0010862	Delayed fine motor development	1	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0032988	Persistent head lag	1	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0002194	Delayed gross motor development	1	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0032988	Persistent head lag	1	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0010862	Delayed fine motor development	1	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0002194	Delayed gross motor development	1	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0010862	Delayed fine motor development	1	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0032988	Persistent head lag	1	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0002194	Delayed gross motor development	1	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0010862	Delayed fine motor development	1	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0032988	Persistent head lag	1	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0002194	Delayed gross motor development	1	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0002194	Delayed gross motor development	1	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0032988	Persistent head lag	1	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0010862	Delayed fine motor development	1	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0002194	Delayed gross motor development	1	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0010862	Delayed fine motor development	1	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0032988	Persistent head lag	1	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0002194	Delayed gross motor development	1	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0032988	Persistent head lag	1	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0010862	Delayed fine motor development	1	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0010862	Delayed fine motor development	1	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0032988	Persistent head lag	1	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0002194	Delayed gross motor development	1	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0032988	Persistent head lag	1	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0010862	Delayed fine motor development	1	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0002194	Delayed gross motor development	1	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0002194	Delayed gross motor development	1	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0032988	Persistent head lag	1	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0010862	Delayed fine motor development	1	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0032988	Persistent head lag	1	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0010862	Delayed fine motor development	1	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0002194	Delayed gross motor development	1	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0002194	Delayed gross motor development	1	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0010862	Delayed fine motor development	1	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0032988	Persistent head lag	1	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0032988	Persistent head lag	1	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0010862	Delayed fine motor development	1	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0002194	Delayed gross motor development	1	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0002194	Delayed gross motor development	1	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0010862	Delayed fine motor development	1	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0032988	Persistent head lag	1	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0002194	Delayed gross motor development	1	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0032988	Persistent head lag	1	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0010862	Delayed fine motor development	1	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0002194	Delayed gross motor development	1	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0032988	Persistent head lag	1	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0010862	Delayed fine motor development	1	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0002194	Delayed gross motor development	1	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0010862	Delayed fine motor development	1	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0032988	Persistent head lag	1	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0010862	Delayed fine motor development	1	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0032988	Persistent head lag	1	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0002194	Delayed gross motor development	1	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0010862	Delayed fine motor development	1	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0032988	Persistent head lag	1	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0002194	Delayed gross motor development	1	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0002194	Delayed gross motor development	1	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0010862	Delayed fine motor development	1	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0032988	Persistent head lag	1	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0002194	Delayed gross motor development	1	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0002194	Delayed gross motor development	1	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0010862	Delayed fine motor development	1	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0010862	Delayed fine motor development	1	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0032988	Persistent head lag	1	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0032988	Persistent head lag	1	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0002194	Delayed gross motor development	1	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0032988	Persistent head lag	1	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0010862	Delayed fine motor development	1	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0002194	Delayed gross motor development	1	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0010862	Delayed fine motor development	1	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0032988	Persistent head lag	1	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0010862	Delayed fine motor development	1	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0032988	Persistent head lag	1	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0002194	Delayed gross motor development	1	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0032988	Persistent head lag	1	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0010862	Delayed fine motor development	1	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0002194	Delayed gross motor development	1	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0032988	Persistent head lag	1	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0010862	Delayed fine motor development	1	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0002194	Delayed gross motor development	1	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0002194	Delayed gross motor development	1	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0010862	Delayed fine motor development	1	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0032988	Persistent head lag	1	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0032988	Persistent head lag	1	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0010862	Delayed fine motor development	1	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0002194	Delayed gross motor development	1	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0002194	Delayed gross motor development	1	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0010862	Delayed fine motor development	1	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0032988	Persistent head lag	1	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0002194	Delayed gross motor development	1	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0032988	Persistent head lag	1	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0010862	Delayed fine motor development	1	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0002194	Delayed gross motor development	1	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0032988	Persistent head lag	1	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0010862	Delayed fine motor development	1	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0010862	Delayed fine motor development	1	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0032988	Persistent head lag	1	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0002194	Delayed gross motor development	1	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0002194	Delayed gross motor development	1	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0032988	Persistent head lag	1	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0010862	Delayed fine motor development	1	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0002194	Delayed gross motor development	1	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0032988	Persistent head lag	1	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0010862	Delayed fine motor development	1	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0002194	Delayed gross motor development	1	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0010862	Delayed fine motor development	1	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0032988	Persistent head lag	1	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0002194	Delayed gross motor development	1	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0010862	Delayed fine motor development	1	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0032988	Persistent head lag	1	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0010862	Delayed fine motor development	1	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0032988	Persistent head lag	1	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0002194	Delayed gross motor development	1	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0002194	Delayed gross motor development	1	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0032988	Persistent head lag	1	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0010862	Delayed fine motor development	1	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0002194	Delayed gross motor development	1	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0032988	Persistent head lag	1	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0010862	Delayed fine motor development	1	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0002194	Delayed gross motor development	1	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0032988	Persistent head lag	1	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0010862	Delayed fine motor development	1	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0002194	Delayed gross motor development	1	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0032988	Persistent head lag	1	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0010862	Delayed fine motor development	1	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0032988	Persistent head lag	1	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0010862	Delayed fine motor development	1	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0002194	Delayed gross motor development	1	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0002194	Delayed gross motor development	1	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0032988	Persistent head lag	1	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0010862	Delayed fine motor development	1	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0032988	Persistent head lag	1	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0010862	Delayed fine motor development	1	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0002194	Delayed gross motor development	1	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0002194	Delayed gross motor development	1	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0032988	Persistent head lag	1	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0010862	Delayed fine motor development	1	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0002194	Delayed gross motor development	1	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0010862	Delayed fine motor development	1	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0032988	Persistent head lag	1	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0002194	Delayed gross motor development	1	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0010862	Delayed fine motor development	1	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0032988	Persistent head lag	1	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0002194	Delayed gross motor development	1	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0032988	Persistent head lag	1	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0010862	Delayed fine motor development	1	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0010862	Delayed fine motor development	1	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0032988	Persistent head lag	1	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0002194	Delayed gross motor development	1	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0002194	Delayed gross motor development	1	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0032988	Persistent head lag	1	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0010862	Delayed fine motor development	1	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0002194	Delayed gross motor development	1	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0010862	Delayed fine motor development	1	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0032988	Persistent head lag	1	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0032988	Persistent head lag	1	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0010862	Delayed fine motor development	1	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0002194	Delayed gross motor development	1	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0002194	Delayed gross motor development	1	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0032988	Persistent head lag	1	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0010862	Delayed fine motor development	1	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0010862	Delayed fine motor development	1	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0032988	Persistent head lag	1	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0002194	Delayed gross motor development	1	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0032988	Persistent head lag	1	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0010862	Delayed fine motor development	1	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0002194	Delayed gross motor development	1	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0002194	Delayed gross motor development	1	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0010862	Delayed fine motor development	1	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0032988	Persistent head lag	1	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0002194	Delayed gross motor development	1	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0010862	Delayed fine motor development	1	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0032988	Persistent head lag	1	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0010862	Delayed fine motor development	1	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0032988	Persistent head lag	1	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0002194	Delayed gross motor development	1	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0002194	Delayed gross motor development	1	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0032988	Persistent head lag	1	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0010862	Delayed fine motor development	1	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0010862	Delayed fine motor development	1	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0032988	Persistent head lag	1	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0002194	Delayed gross motor development	1	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0002194	Delayed gross motor development	1	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0010862	Delayed fine motor development	1	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0032988	Persistent head lag	1	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0002194	Delayed gross motor development	1	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0010862	Delayed fine motor development	1	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0032988	Persistent head lag	1	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0002194	Delayed gross motor development	1	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0032988	Persistent head lag	1	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0010862	Delayed fine motor development	1	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0002194	Delayed gross motor development	1	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0010862	Delayed fine motor development	1	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0032988	Persistent head lag	1	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0002194	Delayed gross motor development	1	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0010862	Delayed fine motor development	1	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0032988	Persistent head lag	1	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0010862	Delayed fine motor development	1	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0032988	Persistent head lag	1	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0002194	Delayed gross motor development	1	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0010862	Delayed fine motor development	1	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0032988	Persistent head lag	1	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0002194	Delayed gross motor development	1	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0002194	Delayed gross motor development	1	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0010862	Delayed fine motor development	1	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0032988	Persistent head lag	1	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0002194	Delayed gross motor development	1	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0010862	Delayed fine motor development	1	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0032988	Persistent head lag	1	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0002194	Delayed gross motor development	1	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0032988	Persistent head lag	1	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0010862	Delayed fine motor development	1	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0002194	Delayed gross motor development	1	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0032988	Persistent head lag	1	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0010862	Delayed fine motor development	1	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0010862	Delayed fine motor development	1	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0032988	Persistent head lag	1	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0002194	Delayed gross motor development	1	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0032988	Persistent head lag	1	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0010862	Delayed fine motor development	1	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0002194	Delayed gross motor development	1	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0010862	Delayed fine motor development	1	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0032988	Persistent head lag	1	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0002194	Delayed gross motor development	1	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0002194	Delayed gross motor development	1	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0032988	Persistent head lag	1	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0010862	Delayed fine motor development	1	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0010862	Delayed fine motor development	1	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0032988	Persistent head lag	1	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0002194	Delayed gross motor development	1	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0002194	Delayed gross motor development	1	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0010862	Delayed fine motor development	1	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0032988	Persistent head lag	1	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0010862	Delayed fine motor development	1	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0032988	Persistent head lag	1	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0002194	Delayed gross motor development	1	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0002194	Delayed gross motor development	1	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0032988	Persistent head lag	1	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0010862	Delayed fine motor development	1	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0002194	Delayed gross motor development	1	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0032988	Persistent head lag	1	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0010862	Delayed fine motor development	1	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0032988	Persistent head lag	1	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0010862	Delayed fine motor development	1	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0002194	Delayed gross motor development	1	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0010862	Delayed fine motor development	1	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0032988	Persistent head lag	1	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0002194	Delayed gross motor development	1	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0002194	Delayed gross motor development	1	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0010862	Delayed fine motor development	1	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0032988	Persistent head lag	1	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0002194	Delayed gross motor development	1	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0032988	Persistent head lag	1	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0010862	Delayed fine motor development	1	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0002194	Delayed gross motor development	1	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0010862	Delayed fine motor development	1	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0032988	Persistent head lag	1	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0002194	Delayed gross motor development	1	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0032988	Persistent head lag	1	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0010862	Delayed fine motor development	1	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0032988	Persistent head lag	1	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0010862	Delayed fine motor development	1	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0002194	Delayed gross motor development	1	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0010862	Delayed fine motor development	1	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0032988	Persistent head lag	1	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0010862	Delayed fine motor development	1	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0032988	Persistent head lag	1	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0002194	Delayed gross motor development	1	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0010862	Delayed fine motor development	1	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0032988	Persistent head lag	1	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0002194	Delayed gross motor development	1	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0032988	Persistent head lag	1	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0010862	Delayed fine motor development	1	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0002194	Delayed gross motor development	1	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0010862	Delayed fine motor development	1	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0032988	Persistent head lag	1	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0002194	Delayed gross motor development	1	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0002194	Delayed gross motor development	1	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0010862	Delayed fine motor development	1	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0032988	Persistent head lag	1	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0002194	Delayed gross motor development	1	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0010862	Delayed fine motor development	1	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0032988	Persistent head lag	1	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0010862	Delayed fine motor development	1	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0032988	Persistent head lag	1	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0002194	Delayed gross motor development	1	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0002194	Delayed gross motor development	1	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0032988	Persistent head lag	1	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0010862	Delayed fine motor development	1	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0010862	Delayed fine motor development	1	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0032988	Persistent head lag	1	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0002194	Delayed gross motor development	1	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0002194	Delayed gross motor development	1	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0032988	Persistent head lag	1	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0010862	Delayed fine motor development	1	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0002194	Delayed gross motor development	1	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0032988	Persistent head lag	1	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0010862	Delayed fine motor development	1	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0002194	Delayed gross motor development	1	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0032988	Persistent head lag	1	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0010862	Delayed fine motor development	1	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0002194	Delayed gross motor development	1	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0010862	Delayed fine motor development	1	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0032988	Persistent head lag	1	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0002194	Delayed gross motor development	1	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0010862	Delayed fine motor development	1	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0032988	Persistent head lag	1	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0002194	Delayed gross motor development	1	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0032988	Persistent head lag	1	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0010862	Delayed fine motor development	1	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0032988	Persistent head lag	1	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0032988	Persistent head lag	1	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0032988	Persistent head lag	1	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0032988	Persistent head lag	1	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0002194	Delayed gross motor development	1	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0010862	Delayed fine motor development	1	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0032988	Persistent head lag	1	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0010862	Delayed fine motor development	1	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0032988	Persistent head lag	1	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0002194	Delayed gross motor development	1	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0002194	Delayed gross motor development	1	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0032988	Persistent head lag	1	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0010862	Delayed fine motor development	1	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0010862	Delayed fine motor development	1	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0032988	Persistent head lag	1	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0002194	Delayed gross motor development	1	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0002194	Delayed gross motor development	1	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0032988	Persistent head lag	1	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0010862	Delayed fine motor development	1	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0032988	Persistent head lag	1	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0010862	Delayed fine motor development	1	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0002194	Delayed gross motor development	1	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0002194	Delayed gross motor development	1	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0010862	Delayed fine motor development	1	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0032988	Persistent head lag	1	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0002194	Delayed gross motor development	1	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0032988	Persistent head lag	1	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0010862	Delayed fine motor development	1	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0002194	Delayed gross motor development	1	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0032988	Persistent head lag	1	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0010862	Delayed fine motor development	1	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0002194	Delayed gross motor development	1	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0010862	Delayed fine motor development	1	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0032988	Persistent head lag	1	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0002194	Delayed gross motor development	1	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0010862	Delayed fine motor development	1	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0032988	Persistent head lag	1	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0010862	Delayed fine motor development	1	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0032988	Persistent head lag	1	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0002194	Delayed gross motor development	1	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0002194	Delayed gross motor development	1	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0010862	Delayed fine motor development	1	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0032988	Persistent head lag	1	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0002194	Delayed gross motor development	1	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0010862	Delayed fine motor development	1	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0032988	Persistent head lag	1	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0002194	Delayed gross motor development	1	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0010862	Delayed fine motor development	1	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0032988	Persistent head lag	1	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0002194	Delayed gross motor development	1	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0010862	Delayed fine motor development	1	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0032988	Persistent head lag	1	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0010862	Delayed fine motor development	1	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0032988	Persistent head lag	1	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0002194	Delayed gross motor development	1	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0002194	Delayed gross motor development	1	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0010862	Delayed fine motor development	1	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0032988	Persistent head lag	1	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0002194	Delayed gross motor development	1	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0010862	Delayed fine motor development	1	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0032988	Persistent head lag	1	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0002194	Delayed gross motor development	1	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0010862	Delayed fine motor development	1	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0032988	Persistent head lag	1	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0010862	Delayed fine motor development	1	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0032988	Persistent head lag	1	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0002194	Delayed gross motor development	1	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0010862	Delayed fine motor development	1	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0032988	Persistent head lag	1	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0002194	Delayed gross motor development	1	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0002194	Delayed gross motor development	1	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0032988	Persistent head lag	1	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0010862	Delayed fine motor development	1	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0002194	Delayed gross motor development	1	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0010862	Delayed fine motor development	1	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0032988	Persistent head lag	1	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0032988	Persistent head lag	1	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0010862	Delayed fine motor development	1	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0002194	Delayed gross motor development	1	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0002194	Delayed gross motor development	1	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0032988	Persistent head lag	1	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0010862	Delayed fine motor development	1	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0032988	Persistent head lag	1	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0010862	Delayed fine motor development	1	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0002194	Delayed gross motor development	1	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0032988	Persistent head lag	1	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0010862	Delayed fine motor development	1	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0002194	Delayed gross motor development	1	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0002194	Delayed gross motor development	1	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0010862	Delayed fine motor development	1	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0032988	Persistent head lag	1	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0032988	Persistent head lag	1	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0032988	Persistent head lag	1	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0032988	Persistent head lag	1	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0032988	Persistent head lag	1	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0032988	Persistent head lag	1	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0032988	Persistent head lag	1	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0032988	Persistent head lag	1	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0032988	Persistent head lag	1	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0002194	Delayed gross motor development	1	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0010862	Delayed fine motor development	1	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0032988	Persistent head lag	1	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0002194	Delayed gross motor development	1	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0032988	Persistent head lag	1	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0010862	Delayed fine motor development	1	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0002194	Delayed gross motor development	1	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0010862	Delayed fine motor development	1	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0032988	Persistent head lag	1	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0032988	Persistent head lag	1	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0010862	Delayed fine motor development	1	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0002194	Delayed gross motor development	1	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0002194	Delayed gross motor development	1	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0010862	Delayed fine motor development	1	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0032988	Persistent head lag	1	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0032988	Persistent head lag	1	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0010862	Delayed fine motor development	1	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0002194	Delayed gross motor development	1	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0002194	Delayed gross motor development	1	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0010862	Delayed fine motor development	1	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0032988	Persistent head lag	1	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0010862	Delayed fine motor development	1	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0032988	Persistent head lag	1	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0002194	Delayed gross motor development	1	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0010862	Delayed fine motor development	1	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0032988	Persistent head lag	1	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0002194	Delayed gross motor development	1	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0002194	Delayed gross motor development	1	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0010862	Delayed fine motor development	1	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0032988	Persistent head lag	1	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0032988	Persistent head lag	1	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0010862	Delayed fine motor development	1	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0002194	Delayed gross motor development	1	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0002194	Delayed gross motor development	1	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0010862	Delayed fine motor development	1	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0032988	Persistent head lag	1	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0010862	Delayed fine motor development	1	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0032988	Persistent head lag	1	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0002194	Delayed gross motor development	1	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0002194	Delayed gross motor development	1	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0032988	Persistent head lag	1	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0010862	Delayed fine motor development	1	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0002194	Delayed gross motor development	1	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0010862	Delayed fine motor development	1	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0032988	Persistent head lag	1	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0002194	Delayed gross motor development	1	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0032988	Persistent head lag	1	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0010862	Delayed fine motor development	1	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0032988	Persistent head lag	1	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0010862	Delayed fine motor development	1	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0002194	Delayed gross motor development	1	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0002194	Delayed gross motor development	1	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0032988	Persistent head lag	1	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0010862	Delayed fine motor development	1	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0002194	Delayed gross motor development	1	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0010862	Delayed fine motor development	1	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0032988	Persistent head lag	1	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0002194	Delayed gross motor development	1	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0032988	Persistent head lag	1	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0010862	Delayed fine motor development	1	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0032988	Persistent head lag	1	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0010862	Delayed fine motor development	1	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0002194	Delayed gross motor development	1	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0002194	Delayed gross motor development	1	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0010862	Delayed fine motor development	1	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0032988	Persistent head lag	1	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0032988	Persistent head lag	1	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0010862	Delayed fine motor development	1	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0002194	Delayed gross motor development	1	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0002194	Delayed gross motor development	1	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0010862	Delayed fine motor development	1	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0032988	Persistent head lag	1	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0032988	Persistent head lag	1	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0010862	Delayed fine motor development	1	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0002194	Delayed gross motor development	1	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0002194	Delayed gross motor development	1	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0010862	Delayed fine motor development	1	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0032988	Persistent head lag	1	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0032988	Persistent head lag	1	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0010862	Delayed fine motor development	1	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0002194	Delayed gross motor development	1	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0002194	Delayed gross motor development	1	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0010862	Delayed fine motor development	1	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0032988	Persistent head lag	1	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0025335	Delayed ability to stand	2	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0025335	Delayed ability to stand	2	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0025336	Delayed ability to sit	2	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0025336	Delayed ability to sit	2	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0032989	Delayed ability to roll over	2	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0032989	Delayed ability to roll over	2	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0031936	Delayed ability to walk	2	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0033128	Delayed ability to crawl	2	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0031936	Delayed ability to walk	2	ABCC8 CL E G H	6833	99886				ORPHA	1	1892	59	600509
HP:0001270	HP:0033128	Delayed ability to crawl	2	ABCC8 CL E G H	6833	99885				ORPHA	1	1892	59	600509
HP:0001270	HP:0032989	Delayed ability to roll over	2	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0033128	Delayed ability to crawl	2	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0031936	Delayed ability to walk	2	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0025335	Delayed ability to stand	2	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0025336	Delayed ability to sit	2	ABCC8 CL E G H	6833	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	1892	59	600509
HP:0001270	HP:0025336	Delayed ability to sit	2	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0032989	Delayed ability to roll over	2	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0033128	Delayed ability to crawl	2	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0031936	Delayed ability to walk	2	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0025335	Delayed ability to stand	2	ACADSB CL E G H	36	610006	Deficiency of 2-methylbutyryl-CoA dehydrogenase	610006	C1864912	OMIM	1	337	91	600301
HP:0001270	HP:0025336	Delayed ability to sit	2	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0025336	Delayed ability to sit	2	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0032989	Delayed ability to roll over	2	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0032989	Delayed ability to roll over	2	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0025335	Delayed ability to stand	2	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0032989	Delayed ability to roll over	2	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0033128	Delayed ability to crawl	2	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0033128	Delayed ability to crawl	2	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0031936	Delayed ability to walk	2	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0025336	Delayed ability to sit	2	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0033128	Delayed ability to crawl	2	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0031936	Delayed ability to walk	2	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0031936	Delayed ability to walk	2	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0025335	Delayed ability to stand	2	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0032989	Delayed ability to roll over	2	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0025335	Delayed ability to stand	2	ACTA1 CL E G H	58	2020				ORPHA	1	506	129	102610
HP:0001270	HP:0025335	Delayed ability to stand	2	ACTA1 CL E G H	58	171439				ORPHA	1	506	129	102610
HP:0001270	HP:0025336	Delayed ability to sit	2	ACTA1 CL E G H	58	171433				ORPHA	1	506	129	102610
HP:0001270	HP:0033128	Delayed ability to crawl	2	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0031936	Delayed ability to walk	2	ACTA1 CL E G H	58	171430				ORPHA	1	506	129	102610
HP:0001270	HP:0025336	Delayed ability to sit	2	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0032989	Delayed ability to roll over	2	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0033128	Delayed ability to crawl	2	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0031936	Delayed ability to walk	2	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0025335	Delayed ability to stand	2	ACTA1 CL E G H	58	161800	Nemaline myopathy 3	161800	C3711389	OMIM	1	506	129	102610
HP:0001270	HP:0033128	Delayed ability to crawl	2	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0031936	Delayed ability to walk	2	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0025335	Delayed ability to stand	2	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0025336	Delayed ability to sit	2	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0032989	Delayed ability to roll over	2	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ADA2 CL E G H	51816	820				ORPHA	1	533	1839	607575
HP:0001270	HP:0033128	Delayed ability to crawl	2	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0031936	Delayed ability to walk	2	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0025335	Delayed ability to stand	2	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0025336	Delayed ability to sit	2	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0032989	Delayed ability to roll over	2	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ADAMTS2 CL E G H	9509	225410	Ehlers-Danlos syndrome, type vii, autosomal recessive	225410	C2700425	OMIM	1	1499	218	604539
HP:0001270	HP:0033128	Delayed ability to crawl	2	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0031936	Delayed ability to walk	2	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0025335	Delayed ability to stand	2	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0025336	Delayed ability to sit	2	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0032989	Delayed ability to roll over	2	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0033257	Delayed ability to walk with support	2	AGK CL E G H	55750	212350	Cataract and cardiomyopathy	212350	C1859317	OMIM	1	347	21869	610345
HP:0001270	HP:0031936	Delayed ability to walk	2	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0033128	Delayed ability to crawl	2	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0025335	Delayed ability to stand	2	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0025336	Delayed ability to sit	2	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0032989	Delayed ability to roll over	2	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0033257	Delayed ability to walk with support	2	AGTPBP1 CL E G H	23287	618276	618276	618276		OMIM	1	105	17258	606830
HP:0001270	HP:0033128	Delayed ability to crawl	2	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0031936	Delayed ability to walk	2	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0025335	Delayed ability to stand	2	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0025336	Delayed ability to sit	2	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0032989	Delayed ability to roll over	2	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0033257	Delayed ability to walk with support	2	AHCY CL E G H	191	613752	Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency	613752	C3151058	OMIM	1	255	343	180960
HP:0001270	HP:0033128	Delayed ability to crawl	2	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0031936	Delayed ability to walk	2	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0025335	Delayed ability to stand	2	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0025336	Delayed ability to sit	2	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0032989	Delayed ability to roll over	2	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ALDH18A1 CL E G H	5832	447760				ORPHA	1	586	9722	138250
HP:0001270	HP:0032989	Delayed ability to roll over	2	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0033128	Delayed ability to crawl	2	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0031936	Delayed ability to walk	2	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0025335	Delayed ability to stand	2	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0025336	Delayed ability to sit	2	ALDH5A1 CL E G H	7915	271980	Succinate-semialdehyde dehydrogenase deficiency	271980	C0268631	OMIM	1	763	408	610045
HP:0001270	HP:0031936	Delayed ability to walk	2	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0033128	Delayed ability to crawl	2	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0025335	Delayed ability to stand	2	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0025336	Delayed ability to sit	2	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0032989	Delayed ability to roll over	2	ALG14 CL E G H	199857	353327				ORPHA	1	144	28287	612866
HP:0001270	HP:0025336	Delayed ability to sit	2	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0032989	Delayed ability to roll over	2	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0033128	Delayed ability to crawl	2	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0031936	Delayed ability to walk	2	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0025335	Delayed ability to stand	2	ALG2 CL E G H	85365	353327				ORPHA	1	335	23159	607905
HP:0001270	HP:0031936	Delayed ability to walk	2	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0033128	Delayed ability to crawl	2	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0025335	Delayed ability to stand	2	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0025336	Delayed ability to sit	2	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0032989	Delayed ability to roll over	2	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ALS2 CL E G H	57679	607225	Infantile-onset ascending hereditary spastic paralysis	607225	C2931441	OMIM	1	947	443	606352
HP:0001270	HP:0033128	Delayed ability to crawl	2	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0031936	Delayed ability to walk	2	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0025335	Delayed ability to stand	2	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0025336	Delayed ability to sit	2	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0032989	Delayed ability to roll over	2	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0033257	Delayed ability to walk with support	2	AP3B1 CL E G H	8546	608233	Hermansky Pudlak syndrome 2	608233	C1842362	OMIM	1	677	566	603401
HP:0001270	HP:0025336	Delayed ability to sit	2	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0033257	Delayed ability to walk with support	2	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0032989	Delayed ability to roll over	2	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0031936	Delayed ability to walk	2	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0033128	Delayed ability to crawl	2	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0025335	Delayed ability to stand	2	APOPT1 CL E G H	84334	436271				ORPHA	1	197	20492	616003
HP:0001270	HP:0025336	Delayed ability to sit	2	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0032989	Delayed ability to roll over	2	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0033257	Delayed ability to walk with support	2	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0033128	Delayed ability to crawl	2	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0031936	Delayed ability to walk	2	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0025335	Delayed ability to stand	2	APOPT1 CL E G H	84334	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	197	20492	616003
HP:0001270	HP:0025335	Delayed ability to stand	2	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0025336	Delayed ability to sit	2	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0032989	Delayed ability to roll over	2	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0031936	Delayed ability to walk	2	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0033128	Delayed ability to crawl	2	ARCN1 CL E G H	372	617164	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay	617164	C4310686	OMIM	1	202	649	600820
HP:0001270	HP:0032989	Delayed ability to roll over	2	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0033128	Delayed ability to crawl	2	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0031936	Delayed ability to walk	2	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0025335	Delayed ability to stand	2	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0025336	Delayed ability to sit	2	ARHGEF2 CL E G H	9181	617523	Neurodevelopmental disorder with midbrain and hindbrain malformations	617523	C4479613	OMIM	1	78	682	607560
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0032989	Delayed ability to roll over	2	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0031936	Delayed ability to walk	2	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0033128	Delayed ability to crawl	2	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0025335	Delayed ability to stand	2	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0025336	Delayed ability to sit	2	ARID2 CL E G H	196528	617808	COFFIN-SIRIS SYNDROME 6	617808	C4540499	OMIM	1	313	18037	609539
HP:0001270	HP:0025336	Delayed ability to sit	2	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0032989	Delayed ability to roll over	2	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0031936	Delayed ability to walk	2	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0033128	Delayed ability to crawl	2	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0025335	Delayed ability to stand	2	ASAH1 CL E G H	427	228000	Farber disease	228000	C0268255	OMIM	1	913	735	613468
HP:0001270	HP:0025336	Delayed ability to sit	2	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0032989	Delayed ability to roll over	2	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0033128	Delayed ability to crawl	2	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0031936	Delayed ability to walk	2	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0025335	Delayed ability to stand	2	ASPM CL E G H	259266	608716	Primary autosomal recessive microcephaly 5	608716	C1837501	OMIM	1	1597	19048	605481
HP:0001270	HP:0025336	Delayed ability to sit	2	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0031936	Delayed ability to walk	2	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0025335	Delayed ability to stand	2	ATL1 CL E G H	51062	182600	Spastic paraplegia 3	182600	C2931355	OMIM	1	517	11231	606439
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP1A3 CL E G H	478	71517				ORPHA	1	993	801	182350
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP2B3 CL E G H	492	314978				ORPHA	1	352	816	300014
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP2B3 CL E G H	492	302500	Spinocerebellar ataxia, X-linked 1	302500	C0796205	OMIM	1	352	816	300014
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP6AP2 CL E G H	10159	300423	Mental retardation, X-linked, syndromic, Hedera type	300423	C1845543	OMIM	1	340	18305	300556
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP6V0A2 CL E G H	23545	357074				ORPHA	1	610	18481	611716
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP6V0A2 CL E G H	23545	219200	Cutis laxa with osteodystrophy	219200	C0268355	OMIM	1	610	18481	611716
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP6V1A CL E G H	523	357074				ORPHA	1	229	851	607027
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP6V1A CL E G H	523	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID	617403	C4479409	OMIM	1	229	851	607027
HP:0001270	HP:0025336	Delayed ability to sit	2	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0031936	Delayed ability to walk	2	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0025335	Delayed ability to stand	2	ATP6V1E1 CL E G H	529	357074				ORPHA	1	196	857	108746
HP:0001270	HP:0025335	Delayed ability to stand	2	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0025336	Delayed ability to sit	2	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0031936	Delayed ability to walk	2	ATXN7 CL E G H	6314	94147				ORPHA	1	98	10560	607640
HP:0001270	HP:0025336	Delayed ability to sit	2	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0032989	Delayed ability to roll over	2	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0033257	Delayed ability to walk with support	2	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0033128	Delayed ability to crawl	2	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0031936	Delayed ability to walk	2	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0025335	Delayed ability to stand	2	AUH CL E G H	549	250950	3-Methylglutaconic aciduria type 1	250950	C0342727	OMIM	1	249	890	600529
HP:0001270	HP:0032989	Delayed ability to roll over	2	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0033128	Delayed ability to crawl	2	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0031936	Delayed ability to walk	2	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0025335	Delayed ability to stand	2	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0025336	Delayed ability to sit	2	BCOR CL E G H	54880	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	688	20893	300485
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0032989	Delayed ability to roll over	2	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0031936	Delayed ability to walk	2	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0033128	Delayed ability to crawl	2	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0025335	Delayed ability to stand	2	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0025336	Delayed ability to sit	2	BCOR CL E G H	54880	300166	Oculofaciocardiodental syndrome	300166	C1846265	OMIM	1	688	20893	300485
HP:0001270	HP:0033128	Delayed ability to crawl	2	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0031936	Delayed ability to walk	2	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0025335	Delayed ability to stand	2	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0025336	Delayed ability to sit	2	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0032989	Delayed ability to roll over	2	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BICD2 CL E G H	23299	618291	618291	618291		OMIM	1	740	17208	609797
HP:0001270	HP:0025336	Delayed ability to sit	2	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0032989	Delayed ability to roll over	2	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0033128	Delayed ability to crawl	2	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0031936	Delayed ability to walk	2	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0025335	Delayed ability to stand	2	BICD2 CL E G H	23299	615290	Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant	615290	C3809049	OMIM	1	740	17208	609797
HP:0001270	HP:0025335	Delayed ability to stand	2	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0025336	Delayed ability to sit	2	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0032989	Delayed ability to roll over	2	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0033128	Delayed ability to crawl	2	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0031936	Delayed ability to walk	2	BIN1 CL E G H	274	169186				ORPHA	1	656	1052	601248
HP:0001270	HP:0033128	Delayed ability to crawl	2	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0031936	Delayed ability to walk	2	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0025335	Delayed ability to stand	2	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0025336	Delayed ability to sit	2	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0032989	Delayed ability to roll over	2	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BIN1 CL E G H	274	255200	Autosomal recessive centronuclear myopathy	255200	C0410204	OMIM	1	656	1052	601248
HP:0001270	HP:0025335	Delayed ability to stand	2	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0025336	Delayed ability to sit	2	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0032989	Delayed ability to roll over	2	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0033128	Delayed ability to crawl	2	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0031936	Delayed ability to walk	2	BSND CL E G H	7809	602522	Bartter syndrome type 4	602522	C1865270	OMIM	1	303	16512	606412
HP:0001270	HP:0031936	Delayed ability to walk	2	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0033128	Delayed ability to crawl	2	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0025335	Delayed ability to stand	2	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0025336	Delayed ability to sit	2	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0032989	Delayed ability to roll over	2	CANT1 CL E G H	124583	251450	Desbuquois dysplasia 1	251450	C4012146	OMIM	1	299	19721	613165
HP:0001270	HP:0033128	Delayed ability to crawl	2	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0031936	Delayed ability to walk	2	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0025335	Delayed ability to stand	2	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0025336	Delayed ability to sit	2	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0032989	Delayed ability to roll over	2	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CDC6 CL E G H	990	613805	Meier-Gorlin syndrome 5	613805	C3151126	OMIM	1	146	1744	602627
HP:0001270	HP:0025335	Delayed ability to stand	2	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0025336	Delayed ability to sit	2	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0031936	Delayed ability to walk	2	CHKB CL E G H	1120	602541	Muscular dystrophy, congenital, megaconial type	602541	C1865233	OMIM	1	502	1938	612395
HP:0001270	HP:0025336	Delayed ability to sit	2	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0031936	Delayed ability to walk	2	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0025335	Delayed ability to stand	2	CHRNA1 CL E G H	1134	608930	Congenital myasthenic syndrome 1B, fast-channel	608930	C1837122	OMIM	1	468	1955	100690
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0031936	Delayed ability to walk	2	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0025335	Delayed ability to stand	2	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0025336	Delayed ability to sit	2	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHRNE CL E G H	1145	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	1011	1966	100725
HP:0001270	HP:0025335	Delayed ability to stand	2	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0025336	Delayed ability to sit	2	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0031936	Delayed ability to walk	2	CHST14 CL E G H	113189	601776	Ehlers-Danlos syndrome, musculocontractural type	601776	C1866294	OMIM	1	268	24464	608429
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0031936	Delayed ability to walk	2	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0025335	Delayed ability to stand	2	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0025336	Delayed ability to sit	2	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHST3 CL E G H	9469	263463				ORPHA	1	445	1971	603799
HP:0001270	HP:0033128	Delayed ability to crawl	2	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0031936	Delayed ability to walk	2	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0025335	Delayed ability to stand	2	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0025336	Delayed ability to sit	2	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0032989	Delayed ability to roll over	2	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CIB2 CL E G H	10518	614869	Usher syndrome, type 1J	614869	C3553944	OMIM	1	227	24579	605564
HP:0001270	HP:0033128	Delayed ability to crawl	2	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0031936	Delayed ability to walk	2	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0025335	Delayed ability to stand	2	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0025336	Delayed ability to sit	2	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0032989	Delayed ability to roll over	2	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CLCNKA CL E G H	1187	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	230	2026	602024
HP:0001270	HP:0025336	Delayed ability to sit	2	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0032989	Delayed ability to roll over	2	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0033128	Delayed ability to crawl	2	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0031936	Delayed ability to walk	2	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0025335	Delayed ability to stand	2	CLCNKB CL E G H	1188	613090	Bartter syndrome, type 4b	613090	C2751312	OMIM	1	478	2027	602023
HP:0001270	HP:0031936	Delayed ability to walk	2	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0033128	Delayed ability to crawl	2	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0025335	Delayed ability to stand	2	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0025336	Delayed ability to sit	2	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0032989	Delayed ability to roll over	2	COA7 CL E G H	65260	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	58	25716	615623
HP:0001270	HP:0025336	Delayed ability to sit	2	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0032989	Delayed ability to roll over	2	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0033128	Delayed ability to crawl	2	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0031936	Delayed ability to walk	2	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0025335	Delayed ability to stand	2	COG4 CL E G H	25839	618150	SAUL-WILSON SYNDROME	618150		OMIM	1	339	18620	606976
HP:0001270	HP:0025335	Delayed ability to stand	2	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0025336	Delayed ability to sit	2	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0031936	Delayed ability to walk	2	COL12A1 CL E G H	1303	616470	Ullrich congenital muscular dystrophy 2	616470	C4225314	OMIM	1	2548	2188	120320
HP:0001270	HP:0025336	Delayed ability to sit	2	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0031936	Delayed ability to walk	2	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0025335	Delayed ability to stand	2	COL2A1 CL E G H	1280	156550	Kniest dysplasia	156550	C0265279	OMIM	1	2380	2200	120140
HP:0001270	HP:0025336	Delayed ability to sit	2	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0031936	Delayed ability to walk	2	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0025335	Delayed ability to stand	2	COL6A1 CL E G H	1291	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1718	2211	120220
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0031936	Delayed ability to walk	2	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0025335	Delayed ability to stand	2	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0025336	Delayed ability to sit	2	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL6A1 CL E G H	1291	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1718	2211	120220
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0031936	Delayed ability to walk	2	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0025335	Delayed ability to stand	2	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0025336	Delayed ability to sit	2	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL6A2 CL E G H	1292	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	1928	2212	120240
HP:0001270	HP:0025336	Delayed ability to sit	2	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0031936	Delayed ability to walk	2	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0025335	Delayed ability to stand	2	COL6A2 CL E G H	1292	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	1928	2212	120240
HP:0001270	HP:0025336	Delayed ability to sit	2	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0031936	Delayed ability to walk	2	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0025335	Delayed ability to stand	2	COL6A3 CL E G H	1293	158810	Bethlem myopathy 1	158810	CN029274	OMIM	1	3001	2213	120250
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0031936	Delayed ability to walk	2	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0025335	Delayed ability to stand	2	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0025336	Delayed ability to sit	2	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL6A3 CL E G H	1293	254090	Ullrich congenital muscular dystrophy 1	254090	CN033863	OMIM	1	3001	2213	120250
HP:0001270	HP:0033128	Delayed ability to crawl	2	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0031936	Delayed ability to walk	2	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0025335	Delayed ability to stand	2	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0025336	Delayed ability to sit	2	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0032989	Delayed ability to roll over	2	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COQ2 CL E G H	27235	607426	Coenzyme Q10 deficiency, primary 1	607426	C1843920	OMIM	1	346	25223	609825
HP:0001270	HP:0025335	Delayed ability to stand	2	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0025336	Delayed ability to sit	2	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0032989	Delayed ability to roll over	2	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0033128	Delayed ability to crawl	2	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0031936	Delayed ability to walk	2	COQ7 CL E G H	10229	616733	Coenzyme Q10 deficiency, primary, 8	616733	C4225226	OMIM	1	203	2244	601683
HP:0001270	HP:0031936	Delayed ability to walk	2	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0033128	Delayed ability to crawl	2	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0025335	Delayed ability to stand	2	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0025336	Delayed ability to sit	2	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0032989	Delayed ability to roll over	2	COX10 CL E G H	1352	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	356	2260	602125
HP:0001270	HP:0025336	Delayed ability to sit	2	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0032989	Delayed ability to roll over	2	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0033128	Delayed ability to crawl	2	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0031936	Delayed ability to walk	2	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0025335	Delayed ability to stand	2	COX14 CL E G H	84987	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	38	28216	614478
HP:0001270	HP:0031936	Delayed ability to walk	2	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0033128	Delayed ability to crawl	2	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0025335	Delayed ability to stand	2	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0025336	Delayed ability to sit	2	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0032989	Delayed ability to roll over	2	COX20 CL E G H	116228	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	206	26970	614698
HP:0001270	HP:0025336	Delayed ability to sit	2	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0032989	Delayed ability to roll over	2	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0033128	Delayed ability to crawl	2	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0031936	Delayed ability to walk	2	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0025335	Delayed ability to stand	2	COX6B1 CL E G H	1340	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	68	2280	124089
HP:0001270	HP:0033128	Delayed ability to crawl	2	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0031936	Delayed ability to walk	2	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0025335	Delayed ability to stand	2	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0025336	Delayed ability to sit	2	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0032989	Delayed ability to roll over	2	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COX8A CL E G H	1351	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	32	2294	123870
HP:0001270	HP:0025336	Delayed ability to sit	2	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0032989	Delayed ability to roll over	2	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0033128	Delayed ability to crawl	2	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0031936	Delayed ability to walk	2	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0025335	Delayed ability to stand	2	CRAT CL E G H	1384	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8	617917	CN895591	OMIM	1	230	2342	600184
HP:0001270	HP:0025335	Delayed ability to stand	2	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0025336	Delayed ability to sit	2	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0032989	Delayed ability to roll over	2	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0033128	Delayed ability to crawl	2	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0031936	Delayed ability to walk	2	CTBP1 CL E G H	1487	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME	617915	CN895589	OMIM	1	352	2494	602618
HP:0001270	HP:0032989	Delayed ability to roll over	2	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0031936	Delayed ability to walk	2	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0033128	Delayed ability to crawl	2	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0025335	Delayed ability to stand	2	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0025336	Delayed ability to sit	2	CTDP1 CL E G H	9150	604168	Congenital Cataracts, Facial Dysmorphism, and Neuropathy	604168	C1858726	OMIM	1	637	2498	604927
HP:0001270	HP:0033128	Delayed ability to crawl	2	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0031936	Delayed ability to walk	2	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0025335	Delayed ability to stand	2	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0025336	Delayed ability to sit	2	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0032989	Delayed ability to roll over	2	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CYP27B1 CL E G H	1594	264700	Vitamin D-dependent rickets, type 1	264700	C0268689	OMIM	1	236	2606	609506
HP:0001270	HP:0033128	Delayed ability to crawl	2	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0031936	Delayed ability to walk	2	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0025335	Delayed ability to stand	2	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0025336	Delayed ability to sit	2	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0032989	Delayed ability to roll over	2	CYP2U1 CL E G H	113612	615030	Spastic paraplegia 56, autosomal recessive	615030	C3539507	OMIM	1	291	20582	610670
HP:0001270	HP:0031936	Delayed ability to walk	2	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0033128	Delayed ability to crawl	2	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0025335	Delayed ability to stand	2	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0025336	Delayed ability to sit	2	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0032989	Delayed ability to roll over	2	DARS CL E G H	1615	615281	Hypomyelination with brainstem and spinal cord involvement and leg spasticity	615281	C3809008	OMIM	1		2678	603084
HP:0001270	HP:0025336	Delayed ability to sit	2	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0032989	Delayed ability to roll over	2	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0033128	Delayed ability to crawl	2	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0031936	Delayed ability to walk	2	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0025335	Delayed ability to stand	2	DARS2 CL E G H	55157	611105	Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation	611105	C1970180	OMIM	1	397	25538	610956
HP:0001270	HP:0025335	Delayed ability to stand	2	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0025336	Delayed ability to sit	2	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0032989	Delayed ability to roll over	2	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0033128	Delayed ability to crawl	2	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0031936	Delayed ability to walk	2	DCX CL E G H	1641	300067	Lissencephaly, X-linked	300067	C1848199	OMIM	1	423	2714	300121
HP:0001270	HP:0025335	Delayed ability to stand	2	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0025336	Delayed ability to sit	2	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0032989	Delayed ability to roll over	2	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0033128	Delayed ability to crawl	2	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0031936	Delayed ability to walk	2	DMD CL E G H	1756	98896				ORPHA	1	8184	2928	300377
HP:0001270	HP:0032989	Delayed ability to roll over	2	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0033128	Delayed ability to crawl	2	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0031936	Delayed ability to walk	2	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0025335	Delayed ability to stand	2	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0025336	Delayed ability to sit	2	DMXL2 CL E G H	23312	616113	Polyendocrine-polyneuropathy syndrome	616113	C4015261	OMIM	1	1216	2938	612186
HP:0001270	HP:0033128	Delayed ability to crawl	2	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0031936	Delayed ability to walk	2	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0025335	Delayed ability to stand	2	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0025336	Delayed ability to sit	2	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0032989	Delayed ability to roll over	2	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DNM2 CL E G H	1785	160150	Myopathy, centronuclear, 1	160150	C1834558	OMIM	1	1088	2974	602378
HP:0001270	HP:0031936	Delayed ability to walk	2	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0033128	Delayed ability to crawl	2	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0025335	Delayed ability to stand	2	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0025336	Delayed ability to sit	2	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0032989	Delayed ability to roll over	2	DPAGT1 CL E G H	1798	353327				ORPHA	1	312	2995	191350
HP:0001270	HP:0033128	Delayed ability to crawl	2	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0031936	Delayed ability to walk	2	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0025335	Delayed ability to stand	2	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0025336	Delayed ability to sit	2	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0032989	Delayed ability to roll over	2	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DPAGT1 CL E G H	1798	614750	Congenital myasthenic syndrome 13	614750	C3553645	OMIM	1	312	2995	191350
HP:0001270	HP:0032989	Delayed ability to roll over	2	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0033128	Delayed ability to crawl	2	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0031936	Delayed ability to walk	2	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0025335	Delayed ability to stand	2	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0025336	Delayed ability to sit	2	DPYD CL E G H	1806	274270	Dihydropyrimidine dehydrogenase deficiency	274270	C2720286	OMIM	1	446	3012	612779
HP:0001270	HP:0033128	Delayed ability to crawl	2	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0031936	Delayed ability to walk	2	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0025335	Delayed ability to stand	2	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0025336	Delayed ability to sit	2	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0032989	Delayed ability to roll over	2	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0033257	Delayed ability to walk with support	2	DYNC1H1 CL E G H	1778	614228	Charcot-Marie-Tooth disease, axonal, type 2O	614228	C3280220	OMIM	1	3787	2961	600112
HP:0001270	HP:0025335	Delayed ability to stand	2	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0025336	Delayed ability to sit	2	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0032989	Delayed ability to roll over	2	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0033257	Delayed ability to walk with support	2	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0033128	Delayed ability to crawl	2	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0031936	Delayed ability to walk	2	EGR2 CL E G H	1959	605253	Congenital hypomyelinating neuropathy	605253	C0393818	OMIM	1	373	3239	129010
HP:0001270	HP:0033128	Delayed ability to crawl	2	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0031936	Delayed ability to walk	2	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0025335	Delayed ability to stand	2	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0025336	Delayed ability to sit	2	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0032989	Delayed ability to roll over	2	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0033257	Delayed ability to walk with support	2	EGR2 CL E G H	1959	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	373	3239	129010
HP:0001270	HP:0033128	Delayed ability to crawl	2	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0031936	Delayed ability to walk	2	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0025335	Delayed ability to stand	2	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0025336	Delayed ability to sit	2	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0032989	Delayed ability to roll over	2	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0033257	Delayed ability to walk with support	2	EIF2AK3 CL E G H	9451	1667	Dandy-Walker malformation with facial hemangioma			ORPHA	1	520	3255	604032
HP:0001270	HP:0025336	Delayed ability to sit	2	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0032989	Delayed ability to roll over	2	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0033257	Delayed ability to walk with support	2	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0033128	Delayed ability to crawl	2	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0031936	Delayed ability to walk	2	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0025335	Delayed ability to stand	2	EPG5 CL E G H	57724	242840	Vici syndrome	242840	C1855772	OMIM	1	1640	29331	615068
HP:0001270	HP:0033257	Delayed ability to walk with support	2	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0032989	Delayed ability to roll over	2	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0031936	Delayed ability to walk	2	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0033128	Delayed ability to crawl	2	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0025335	Delayed ability to stand	2	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0025336	Delayed ability to sit	2	EXOSC2 CL E G H	23404	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES	617763	C4540367	OMIM	1	277	17097	602238
HP:0001270	HP:0025335	Delayed ability to stand	2	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0025336	Delayed ability to sit	2	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0032989	Delayed ability to roll over	2	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0033257	Delayed ability to walk with support	2	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0033128	Delayed ability to crawl	2	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0031936	Delayed ability to walk	2	EXTL3 CL E G H	2137	617425	Immunoskeletal dysplasia with neurodevelopmental abnormalities	617425	C4479452	OMIM	1	470	3518	605744
HP:0001270	HP:0025336	Delayed ability to sit	2	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0032989	Delayed ability to roll over	2	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0033128	Delayed ability to crawl	2	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0031936	Delayed ability to walk	2	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0025335	Delayed ability to stand	2	FAM126A CL E G H	84668	610532	Hypomyelination and Congenital Cataract	610532	C1864663	OMIM	1		24587	610531
HP:0001270	HP:0025336	Delayed ability to sit	2	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0032989	Delayed ability to roll over	2	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0033128	Delayed ability to crawl	2	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0031936	Delayed ability to walk	2	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0025335	Delayed ability to stand	2	FASTKD2 CL E G H	22868	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	401	29160	612322
HP:0001270	HP:0033128	Delayed ability to crawl	2	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0031936	Delayed ability to walk	2	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0025335	Delayed ability to stand	2	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0025336	Delayed ability to sit	2	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0032989	Delayed ability to roll over	2	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FBN1 CL E G H	2200	284979				ORPHA	1	6619	3603	134797
HP:0001270	HP:0025336	Delayed ability to sit	2	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0032989	Delayed ability to roll over	2	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0033128	Delayed ability to crawl	2	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0031936	Delayed ability to walk	2	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0025335	Delayed ability to stand	2	FBN2 CL E G H	2201	121050	Congenital contractural arachnodactyly	121050	C0220668	OMIM	1	2688	3604	612570
HP:0001270	HP:0025336	Delayed ability to sit	2	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0032989	Delayed ability to roll over	2	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0033128	Delayed ability to crawl	2	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0031936	Delayed ability to walk	2	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0025335	Delayed ability to stand	2	FDX2 CL E G H	112812	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1	125	30546	614585
HP:0001270	HP:0025336	Delayed ability to sit	2	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0032989	Delayed ability to roll over	2	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0033128	Delayed ability to crawl	2	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0031936	Delayed ability to walk	2	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0025335	Delayed ability to stand	2	FGD4 CL E G H	121512	609311	Charcot-Marie-Tooth disease, type 4H	609311	C1836336	OMIM	1	743	19125	611104
HP:0001270	HP:0025336	Delayed ability to sit	2	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0032989	Delayed ability to roll over	2	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0033128	Delayed ability to crawl	2	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0031936	Delayed ability to walk	2	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0025335	Delayed ability to stand	2	FGFR3 CL E G H	2261	100800	Achondroplasia	100800	C0001080	OMIM	1	916	3690	134934
HP:0001270	HP:0025336	Delayed ability to sit	2	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0031936	Delayed ability to walk	2	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0025335	Delayed ability to stand	2	FKBP14 CL E G H	55033	300179				ORPHA	1	220	18625	614505
HP:0001270	HP:0025336	Delayed ability to sit	2	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0031936	Delayed ability to walk	2	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0025335	Delayed ability to stand	2	FKBP14 CL E G H	55033	614557	Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss	614557	C3281160	OMIM	1	220	18625	614505
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0031936	Delayed ability to walk	2	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0025335	Delayed ability to stand	2	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0025336	Delayed ability to sit	2	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKRP CL E G H	79147	370980				ORPHA	1	950	17997	606596
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0031936	Delayed ability to walk	2	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0025335	Delayed ability to stand	2	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0025336	Delayed ability to sit	2	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKRP CL E G H	79147	613153	Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5	613153	C3150413	OMIM	1	950	17997	606596
HP:0001270	HP:0025336	Delayed ability to sit	2	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0031936	Delayed ability to walk	2	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0025335	Delayed ability to stand	2	FKTN CL E G H	2218	370980				ORPHA	1	914	3622	607440
HP:0001270	HP:0025336	Delayed ability to sit	2	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0031936	Delayed ability to walk	2	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0025335	Delayed ability to stand	2	FKTN CL E G H	2218	613152	Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4	613152	C2751052	OMIM	1	914	3622	607440
HP:0001270	HP:0025336	Delayed ability to sit	2	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0031936	Delayed ability to walk	2	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0025335	Delayed ability to stand	2	FKTN CL E G H	2218	611588	Limb-girdle muscular dystrophy-dystroglycanopathy, type C4	611588	C1969040	OMIM	1	914	3622	607440
HP:0001270	HP:0025335	Delayed ability to stand	2	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0025336	Delayed ability to sit	2	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0032989	Delayed ability to roll over	2	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0031936	Delayed ability to walk	2	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0033128	Delayed ability to crawl	2	FLNA CL E G H	2316	309350	Melnick-Needles syndrome	309350	C0025237	OMIM	1	3033	3754	300017
HP:0001270	HP:0033128	Delayed ability to crawl	2	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0031936	Delayed ability to walk	2	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0025335	Delayed ability to stand	2	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0025336	Delayed ability to sit	2	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0032989	Delayed ability to roll over	2	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FOXG1 CL E G H	2290	613454	Rett syndrome, congenital variant	613454	C3150705	OMIM	1	725	3811	164874
HP:0001270	HP:0025336	Delayed ability to sit	2	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0032989	Delayed ability to roll over	2	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0031936	Delayed ability to walk	2	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0033128	Delayed ability to crawl	2	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0025335	Delayed ability to stand	2	GBA CL E G H	2629	231000	Subacute neuronopathic Gaucher's disease	231000	C0268251	OMIM	1		4177	606463
HP:0001270	HP:0032989	Delayed ability to roll over	2	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0033128	Delayed ability to crawl	2	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0031936	Delayed ability to walk	2	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0025335	Delayed ability to stand	2	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0025336	Delayed ability to sit	2	GCK CL E G H	2645	99885				ORPHA	1	947	4195	138079
HP:0001270	HP:0025335	Delayed ability to stand	2	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0025336	Delayed ability to sit	2	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0032989	Delayed ability to roll over	2	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0033128	Delayed ability to crawl	2	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0031936	Delayed ability to walk	2	GCK CL E G H	2645	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	947	4195	138079
HP:0001270	HP:0033128	Delayed ability to crawl	2	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0031936	Delayed ability to walk	2	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0025335	Delayed ability to stand	2	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0025336	Delayed ability to sit	2	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0032989	Delayed ability to roll over	2	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GDAP1 CL E G H	54332	214400	Charcot-Marie-Tooth disease, type 4A	214400	C1859198	OMIM	1	537	15968	606598
HP:0001270	HP:0033128	Delayed ability to crawl	2	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0031936	Delayed ability to walk	2	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0025335	Delayed ability to stand	2	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0025336	Delayed ability to sit	2	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0032989	Delayed ability to roll over	2	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GFM1 CL E G H	85476	609060	Combined oxidative phosphorylation deficiency 1	609060	C1836797	OMIM	1	650	13780	606639
HP:0001270	HP:0025336	Delayed ability to sit	2	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0032989	Delayed ability to roll over	2	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0033128	Delayed ability to crawl	2	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0031936	Delayed ability to walk	2	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0025335	Delayed ability to stand	2	GFPT1 CL E G H	2673	353327				ORPHA	1	524	4241	138292
HP:0001270	HP:0025336	Delayed ability to sit	2	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0032989	Delayed ability to roll over	2	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0031936	Delayed ability to walk	2	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0033128	Delayed ability to crawl	2	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0025335	Delayed ability to stand	2	GFPT1 CL E G H	2673	608931	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency	608931	C1837091	OMIM	1	524	4241	138292
HP:0001270	HP:0025336	Delayed ability to sit	2	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0032989	Delayed ability to roll over	2	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0031936	Delayed ability to walk	2	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0033128	Delayed ability to crawl	2	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0025335	Delayed ability to stand	2	GHR CL E G H	2690	633				ORPHA	1	345	4263	600946
HP:0001270	HP:0025336	Delayed ability to sit	2	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0032989	Delayed ability to roll over	2	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0031936	Delayed ability to walk	2	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0033128	Delayed ability to crawl	2	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0025335	Delayed ability to stand	2	GJB1 CL E G H	2705	1175	CDK4 linked melanoma			ORPHA	1	860	4283	304040
HP:0001270	HP:0032989	Delayed ability to roll over	2	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0033128	Delayed ability to crawl	2	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0031936	Delayed ability to walk	2	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0025335	Delayed ability to stand	2	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0025336	Delayed ability to sit	2	GJB1 CL E G H	2705	302800	X-linked hereditary motor and sensory neuropathy	302800	C0393808	OMIM	1	860	4283	304040
HP:0001270	HP:0025336	Delayed ability to sit	2	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0032989	Delayed ability to roll over	2	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0031936	Delayed ability to walk	2	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0033128	Delayed ability to crawl	2	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0025335	Delayed ability to stand	2	GJC2 CL E G H	57165	608804	Leukodystrophy, hypomyelinating, 2	608804	C1837355	OMIM	1	323	17494	608803
HP:0001270	HP:0031936	Delayed ability to walk	2	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0033128	Delayed ability to crawl	2	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0025335	Delayed ability to stand	2	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0025336	Delayed ability to sit	2	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0032989	Delayed ability to roll over	2	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GMPPB CL E G H	29925	353327				ORPHA	1	364	22932	615320
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0032989	Delayed ability to roll over	2	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0033128	Delayed ability to crawl	2	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0031936	Delayed ability to walk	2	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0025335	Delayed ability to stand	2	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0025336	Delayed ability to sit	2	GRM1 CL E G H	2911	617691	SPINOCEREBELLAR ATAXIA 44	617691	C4521563	OMIM	1	298	4593	604473
HP:0001270	HP:0032989	Delayed ability to roll over	2	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0033128	Delayed ability to crawl	2	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0031936	Delayed ability to walk	2	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0025335	Delayed ability to stand	2	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0025336	Delayed ability to sit	2	GTF2E2 CL E G H	2961	616943	Trichothiodystrophy 6, nonphotosensitive	616943	C4310785	OMIM	1	180	4651	189964
HP:0001270	HP:0033128	Delayed ability to crawl	2	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0031936	Delayed ability to walk	2	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0025335	Delayed ability to stand	2	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0025336	Delayed ability to sit	2	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0032989	Delayed ability to roll over	2	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HACD1 CL E G H	9200	2020				ORPHA	1	159	9639	610467
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0032989	Delayed ability to roll over	2	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0031936	Delayed ability to walk	2	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0033128	Delayed ability to crawl	2	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0025335	Delayed ability to stand	2	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0025336	Delayed ability to sit	2	HEPACAM CL E G H	220296	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	304	26361	611642
HP:0001270	HP:0033128	Delayed ability to crawl	2	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0031936	Delayed ability to walk	2	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0025335	Delayed ability to stand	2	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0025336	Delayed ability to sit	2	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0032989	Delayed ability to roll over	2	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HEPACAM CL E G H	220296	613925	Megalencephalic leukoencephalopathy with subcortical cysts 2a	613925	C3151355	OMIM	1	304	26361	611642
HP:0001270	HP:0025336	Delayed ability to sit	2	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0032989	Delayed ability to roll over	2	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0031936	Delayed ability to walk	2	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0033128	Delayed ability to crawl	2	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0025335	Delayed ability to stand	2	HEPACAM CL E G H	220296	613926	Megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation	613926	C3151356	OMIM	1	304	26361	611642
HP:0001270	HP:0033128	Delayed ability to crawl	2	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0031936	Delayed ability to walk	2	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0025335	Delayed ability to stand	2	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0025336	Delayed ability to sit	2	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0032989	Delayed ability to roll over	2	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HERC2 CL E G H	8924	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	936	4868	605837
HP:0001270	HP:0025336	Delayed ability to sit	2	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0032989	Delayed ability to roll over	2	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0033128	Delayed ability to crawl	2	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0031936	Delayed ability to walk	2	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0025335	Delayed ability to stand	2	HGSNAT CL E G H	138050	252930	Mucopolysaccharidosis, MPS-III-C	252930	C0086649	OMIM	1	1049	26527	610453
HP:0001270	HP:0025335	Delayed ability to stand	2	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0025336	Delayed ability to sit	2	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0032989	Delayed ability to roll over	2	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0033128	Delayed ability to crawl	2	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0031936	Delayed ability to walk	2	HPRT1 CL E G H	3251	300322	Lesch-Nyhan syndrome	300322	C0023374	OMIM	1	354	5157	308000
HP:0001270	HP:0032989	Delayed ability to roll over	2	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0033128	Delayed ability to crawl	2	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0031936	Delayed ability to walk	2	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0025335	Delayed ability to stand	2	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0025336	Delayed ability to sit	2	HYMAI CL E G H	57061	99886				ORPHA	1	18	5326	606546
HP:0001270	HP:0033128	Delayed ability to crawl	2	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0031936	Delayed ability to walk	2	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0025335	Delayed ability to stand	2	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0025336	Delayed ability to sit	2	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0032989	Delayed ability to roll over	2	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IARS2 CL E G H	55699	436174				ORPHA	1	464	29685	612801
HP:0001270	HP:0033128	Delayed ability to crawl	2	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0031936	Delayed ability to walk	2	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0025335	Delayed ability to stand	2	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0025336	Delayed ability to sit	2	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0032989	Delayed ability to roll over	2	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IARS2 CL E G H	55699	616007	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia	616007	C4014942	OMIM	1	464	29685	612801
HP:0001270	HP:0025335	Delayed ability to stand	2	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0025336	Delayed ability to sit	2	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0032989	Delayed ability to roll over	2	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0033128	Delayed ability to crawl	2	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0031936	Delayed ability to walk	2	IFT52 CL E G H	51098	617102	Short-rib thoracic dysplasia 16 with or without polydactyly	617102	C4310718	OMIM	1	166	15901	617094
HP:0001270	HP:0033128	Delayed ability to crawl	2	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0031936	Delayed ability to walk	2	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0025335	Delayed ability to stand	2	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0025336	Delayed ability to sit	2	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0032989	Delayed ability to roll over	2	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IGF1 CL E G H	3479	608747	Insulin-like growth factor I deficiency	608747	C1837475	OMIM	1	197	5464	147440
HP:0001270	HP:0025336	Delayed ability to sit	2	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0032989	Delayed ability to roll over	2	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0033128	Delayed ability to crawl	2	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0031936	Delayed ability to walk	2	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0025335	Delayed ability to stand	2	IGF1R CL E G H	3480	73273				ORPHA	1	926	5465	147370
HP:0001270	HP:0025336	Delayed ability to sit	2	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0032989	Delayed ability to roll over	2	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0033128	Delayed ability to crawl	2	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0031936	Delayed ability to walk	2	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0025335	Delayed ability to stand	2	IGF1R CL E G H	3480	270450	Insulin-like growth factor 1 resistance to	270450	C1849157	OMIM	1	926	5465	147370
HP:0001270	HP:0032989	Delayed ability to roll over	2	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0033128	Delayed ability to crawl	2	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0031936	Delayed ability to walk	2	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0025335	Delayed ability to stand	2	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0025336	Delayed ability to sit	2	IGF2 CL E G H	3481	616489	Growth restriction, severe, with distinctive facies	616489	C4225307	OMIM	1	146	5466	147470
HP:0001270	HP:0025335	Delayed ability to stand	2	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0025336	Delayed ability to sit	2	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0032989	Delayed ability to roll over	2	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0033257	Delayed ability to walk with support	2	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0031936	Delayed ability to walk	2	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0033128	Delayed ability to crawl	2	INPP5K CL E G H	51763	617404	Muscular dystrophy, congenital, with cataracts and intellectual disability	617404	C4479410	OMIM	1	187	33882	607875
HP:0001270	HP:0025335	Delayed ability to stand	2	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0025336	Delayed ability to sit	2	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0032989	Delayed ability to roll over	2	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0033257	Delayed ability to walk with support	2	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0033128	Delayed ability to crawl	2	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0031936	Delayed ability to walk	2	INS CL E G H	3630	99885				ORPHA	1	185	6081	176730
HP:0001270	HP:0032989	Delayed ability to roll over	2	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0033257	Delayed ability to walk with support	2	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0033128	Delayed ability to crawl	2	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0031936	Delayed ability to walk	2	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0025335	Delayed ability to stand	2	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0025336	Delayed ability to sit	2	INS CL E G H	3630	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	185	6081	176730
HP:0001270	HP:0025336	Delayed ability to sit	2	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0032989	Delayed ability to roll over	2	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0033128	Delayed ability to crawl	2	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0031936	Delayed ability to walk	2	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0025335	Delayed ability to stand	2	IPW CL E G H	3653	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	302	6109	601491
HP:0001270	HP:0025336	Delayed ability to sit	2	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0032989	Delayed ability to roll over	2	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0033128	Delayed ability to crawl	2	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0031936	Delayed ability to walk	2	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0025335	Delayed ability to stand	2	ISPD CL E G H	729920	370980				ORPHA	1	733	37276	614631
HP:0001270	HP:0025336	Delayed ability to sit	2	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0032989	Delayed ability to roll over	2	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0033128	Delayed ability to crawl	2	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0031936	Delayed ability to walk	2	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0025335	Delayed ability to stand	2	ITGA7 CL E G H	3679	2020				ORPHA	1	898	6143	600536
HP:0001270	HP:0031936	Delayed ability to walk	2	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0033128	Delayed ability to crawl	2	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0025335	Delayed ability to stand	2	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0025336	Delayed ability to sit	2	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0032989	Delayed ability to roll over	2	ITGA7 CL E G H	3679	613204	Muscular dystrophy, congenital, due to integrin alpha-7 deficiency	613204	C2750786	OMIM	1	898	6143	600536
HP:0001270	HP:0033128	Delayed ability to crawl	2	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0031936	Delayed ability to walk	2	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0025335	Delayed ability to stand	2	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0025336	Delayed ability to sit	2	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0032989	Delayed ability to roll over	2	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ITPR1 CL E G H	3708	206700	Gillespie syndrome	206700	C0431401	OMIM	1	1563	6180	147265
HP:0001270	HP:0025336	Delayed ability to sit	2	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0032989	Delayed ability to roll over	2	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0033128	Delayed ability to crawl	2	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0031936	Delayed ability to walk	2	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0025335	Delayed ability to stand	2	ITPR1 CL E G H	3708	117360	Spinocerebellar ataxia 29	117360	C1861732	OMIM	1	1563	6180	147265
HP:0001270	HP:0025335	Delayed ability to stand	2	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0025336	Delayed ability to sit	2	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0032989	Delayed ability to roll over	2	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0033128	Delayed ability to crawl	2	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0031936	Delayed ability to walk	2	KAT6B CL E G H	23522	603736	Young Simpson syndrome	603736	C1863557	OMIM	1	1003	17582	605880
HP:0001270	HP:0033128	Delayed ability to crawl	2	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0031936	Delayed ability to walk	2	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0025335	Delayed ability to stand	2	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0025336	Delayed ability to sit	2	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0032989	Delayed ability to roll over	2	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KBTBD13 CL E G H	390594	171439				ORPHA	1	530	37227	613727
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNA4 CL E G H	3739	618284	618284	618284		OMIM	1	54	6222	176266
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNC3 CL E G H	3748	98768				ORPHA	1	311	6235	176264
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNC3 CL E G H	3748	605259	Spinocerebellar ataxia 13	605259	C1854488	OMIM	1	311	6235	176264
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNJ11 CL E G H	3767	99886				ORPHA	1	435	6257	600937
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNJ11 CL E G H	3767	99885				ORPHA	1	435	6257	600937
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNJ11 CL E G H	3767	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	435	6257	600937
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0032989	Delayed ability to roll over	2	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0031936	Delayed ability to walk	2	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0033128	Delayed ability to crawl	2	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0025335	Delayed ability to stand	2	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0025336	Delayed ability to sit	2	KDM1A CL E G H	23028	616728	Cleft palate, psychomotor retardation, and distinctive facial features	616728	C4225229	OMIM	1	230	29079	609132
HP:0001270	HP:0031936	Delayed ability to walk	2	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0033128	Delayed ability to crawl	2	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0025335	Delayed ability to stand	2	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0025336	Delayed ability to sit	2	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0032989	Delayed ability to roll over	2	KIF7 CL E G H	374654	607131	Macrocephaly with multiple epiphyseal dysplasia and distinctive facies	607131	C1846722	OMIM	1	1401	30497	611254
HP:0001270	HP:0033128	Delayed ability to crawl	2	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0031936	Delayed ability to walk	2	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0025335	Delayed ability to stand	2	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0025336	Delayed ability to sit	2	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0032989	Delayed ability to roll over	2	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KLC2 CL E G H	64837	609541	Spastic paraplegia, optic atrophy, and neuropathy	609541	C1836010	OMIM	1	104	20716	611729
HP:0001270	HP:0032989	Delayed ability to roll over	2	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0033128	Delayed ability to crawl	2	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0031936	Delayed ability to walk	2	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0025335	Delayed ability to stand	2	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0025336	Delayed ability to sit	2	KLHL40 CL E G H	131377	171430				ORPHA	1	466	30372	615340
HP:0001270	HP:0025336	Delayed ability to sit	2	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0025335	Delayed ability to stand	2	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0025335	Delayed ability to stand	2	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0032989	Delayed ability to roll over	2	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0025336	Delayed ability to sit	2	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0025336	Delayed ability to sit	2	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0033128	Delayed ability to crawl	2	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0031936	Delayed ability to walk	2	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0032989	Delayed ability to roll over	2	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0032989	Delayed ability to roll over	2	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0025335	Delayed ability to stand	2	KLHL41 CL E G H	10324	171439				ORPHA	1	294	16905	607701
HP:0001270	HP:0031936	Delayed ability to walk	2	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0033128	Delayed ability to crawl	2	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0033128	Delayed ability to crawl	2	KLHL41 CL E G H	10324	171433				ORPHA	1	294	16905	607701
HP:0001270	HP:0031936	Delayed ability to walk	2	KLHL41 CL E G H	10324	171430				ORPHA	1	294	16905	607701
HP:0001270	HP:0025336	Delayed ability to sit	2	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0032989	Delayed ability to roll over	2	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0033128	Delayed ability to crawl	2	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0031936	Delayed ability to walk	2	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0025335	Delayed ability to stand	2	KLHL41 CL E G H	10324	615731	Nemaline myopathy 9	615731	C3810384	OMIM	1	294	16905	607701
HP:0001270	HP:0025336	Delayed ability to sit	2	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0032989	Delayed ability to roll over	2	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0033128	Delayed ability to crawl	2	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0031936	Delayed ability to walk	2	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0025335	Delayed ability to stand	2	LAMA1 CL E G H	284217	615960	Poretti-Boltshauser syndrome	615960	C4014821	OMIM	1	1264	6481	150320
HP:0001270	HP:0025336	Delayed ability to sit	2	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0032989	Delayed ability to roll over	2	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0033128	Delayed ability to crawl	2	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0031936	Delayed ability to walk	2	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0025335	Delayed ability to stand	2	LAMA2 CL E G H	3908	607855	Merosin deficient congenital muscular dystrophy	607855	C1263858	OMIM	1	4179	6482	156225
HP:0001270	HP:0031936	Delayed ability to walk	2	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0033128	Delayed ability to crawl	2	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0025335	Delayed ability to stand	2	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0025336	Delayed ability to sit	2	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0032989	Delayed ability to roll over	2	LAMA2 CL E G H	3908	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23	618138		OMIM	1	4179	6482	156225
HP:0001270	HP:0033128	Delayed ability to crawl	2	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0031936	Delayed ability to walk	2	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0025335	Delayed ability to stand	2	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0025336	Delayed ability to sit	2	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0032989	Delayed ability to roll over	2	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LAMA2 CL E G H	3908	258	Schmitt Gillenwater Kelly syndrome			ORPHA	1	4179	6482	156225
HP:0001270	HP:0033128	Delayed ability to crawl	2	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0031936	Delayed ability to walk	2	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0025335	Delayed ability to stand	2	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0025336	Delayed ability to sit	2	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0032989	Delayed ability to roll over	2	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LARGE1 CL E G H	9215	608840	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6	608840	C1837229	OMIM	1	786	6511	603590
HP:0001270	HP:0033128	Delayed ability to crawl	2	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0031936	Delayed ability to walk	2	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0025335	Delayed ability to stand	2	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0025336	Delayed ability to sit	2	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0032989	Delayed ability to roll over	2	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LIAS CL E G H	11019	614462	Pyruvate dehydrogenase lipoic acid synthetase deficiency	614462	C3280887	OMIM	1	410	16429	607031
HP:0001270	HP:0025336	Delayed ability to sit	2	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0032989	Delayed ability to roll over	2	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0033128	Delayed ability to crawl	2	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0031936	Delayed ability to walk	2	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0025335	Delayed ability to stand	2	LMNA CL E G H	4000	613205	Congenital muscular dystrophy, LMNA-related	613205	C2750785	OMIM	1	1814	6636	150330
HP:0001270	HP:0032989	Delayed ability to roll over	2	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0033128	Delayed ability to crawl	2	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0031936	Delayed ability to walk	2	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0025335	Delayed ability to stand	2	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0025336	Delayed ability to sit	2	LMOD3 CL E G H	56203	171430				ORPHA	1	392	6649	616112
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0032989	Delayed ability to roll over	2	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0031936	Delayed ability to walk	2	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0033128	Delayed ability to crawl	2	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0025335	Delayed ability to stand	2	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0025336	Delayed ability to sit	2	LTBP4 CL E G H	8425	98896				ORPHA	1	773	6717	604710
HP:0001270	HP:0033128	Delayed ability to crawl	2	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0031936	Delayed ability to walk	2	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0025335	Delayed ability to stand	2	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0025336	Delayed ability to sit	2	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0032989	Delayed ability to roll over	2	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MAGEL2 CL E G H	54551	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	1013	6814	605283
HP:0001270	HP:0033128	Delayed ability to crawl	2	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0031936	Delayed ability to walk	2	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0025335	Delayed ability to stand	2	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0025336	Delayed ability to sit	2	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0032989	Delayed ability to roll over	2	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MAP3K20 CL E G H	51776	2020				ORPHA	1	368	17797	609479
HP:0001270	HP:0025335	Delayed ability to stand	2	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0025336	Delayed ability to sit	2	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0032989	Delayed ability to roll over	2	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0033128	Delayed ability to crawl	2	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0031936	Delayed ability to walk	2	MAP3K20 CL E G H	51776	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION	617760	C4540345	OMIM	1	368	17797	609479
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0032989	Delayed ability to roll over	2	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0031936	Delayed ability to walk	2	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0033128	Delayed ability to crawl	2	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0025335	Delayed ability to stand	2	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0025336	Delayed ability to sit	2	MAPRE2 CL E G H	10982	616734	Skin creases, congenital symmetric circumferential, 2	616734	C4225225	OMIM	1	73	6891	605789
HP:0001270	HP:0033128	Delayed ability to crawl	2	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0031936	Delayed ability to walk	2	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0025335	Delayed ability to stand	2	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0025336	Delayed ability to sit	2	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0032989	Delayed ability to roll over	2	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MBD5 CL E G H	55777	156200	Mental retardation, autosomal dominant 1	156200	C1969562	OMIM	1	1375	20444	611472
HP:0001270	HP:0033128	Delayed ability to crawl	2	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0031936	Delayed ability to walk	2	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0025335	Delayed ability to stand	2	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0025336	Delayed ability to sit	2	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0032989	Delayed ability to roll over	2	MCM3AP CL E G H	8888	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT	618124	CN253838	OMIM	1	1245	6946	603294
HP:0001270	HP:0025335	Delayed ability to stand	2	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0025336	Delayed ability to sit	2	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0032989	Delayed ability to roll over	2	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0033128	Delayed ability to crawl	2	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0031936	Delayed ability to walk	2	MED12 CL E G H	9968	305450	FG syndrome	305450	C0220769	OMIM	1	1573	11957	300188
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0032989	Delayed ability to roll over	2	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0031936	Delayed ability to walk	2	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0033128	Delayed ability to crawl	2	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0025335	Delayed ability to stand	2	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0025336	Delayed ability to sit	2	MED13L CL E G H	23389	616789	Mental retardation and distinctive facial features with or without cardiac defects	616789	C4225208	OMIM	1	1047	22962	608771
HP:0001270	HP:0025336	Delayed ability to sit	2	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0032989	Delayed ability to roll over	2	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0033128	Delayed ability to crawl	2	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0031936	Delayed ability to walk	2	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0025335	Delayed ability to stand	2	MEF2C CL E G H	4208	613443	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations	613443	C3150700	OMIM	1	515	6996	600662
HP:0001270	HP:0025336	Delayed ability to sit	2	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0032989	Delayed ability to roll over	2	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0031936	Delayed ability to walk	2	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0033128	Delayed ability to crawl	2	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0025335	Delayed ability to stand	2	MEGF10 CL E G H	84466	614399	Myopathy, areflexia, respiratory distress, and dysphagia, early-onset	614399	C3280679	OMIM	1	969	29634	612453
HP:0001270	HP:0025336	Delayed ability to sit	2	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0032989	Delayed ability to roll over	2	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0033128	Delayed ability to crawl	2	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0031936	Delayed ability to walk	2	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0025335	Delayed ability to stand	2	MICU1 CL E G H	10367	615673	Myopathy with extrapyramidal signs	615673	C3810285	OMIM	1	265	1530	605084
HP:0001270	HP:0025336	Delayed ability to sit	2	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0032989	Delayed ability to roll over	2	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0033128	Delayed ability to crawl	2	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0031936	Delayed ability to walk	2	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0025335	Delayed ability to stand	2	MKRN3 CL E G H	7681	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	357	7114	603856
HP:0001270	HP:0033128	Delayed ability to crawl	2	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0031936	Delayed ability to walk	2	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0025335	Delayed ability to stand	2	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0025336	Delayed ability to sit	2	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0032989	Delayed ability to roll over	2	MKRN3-AS1 CL E G H	10108	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1		12910	603857
HP:0001270	HP:0025335	Delayed ability to stand	2	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0025336	Delayed ability to sit	2	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0032989	Delayed ability to roll over	2	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0033128	Delayed ability to crawl	2	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0031936	Delayed ability to walk	2	MLC1 CL E G H	23209	604004	Megalencephalic leukoencephalopathy with subcortical cysts 1	604004	C1858854	OMIM	1	677	17082	605908
HP:0001270	HP:0031936	Delayed ability to walk	2	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0033128	Delayed ability to crawl	2	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0025335	Delayed ability to stand	2	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0025336	Delayed ability to sit	2	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0032989	Delayed ability to roll over	2	MMP13 CL E G H	4322	250400	Metaphyseal chondrodysplasia, Spahr type	250400	C0432225	OMIM	1	274	7159	600108
HP:0001270	HP:0025336	Delayed ability to sit	2	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0032989	Delayed ability to roll over	2	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0033128	Delayed ability to crawl	2	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0031936	Delayed ability to walk	2	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0025335	Delayed ability to stand	2	MPDZ CL E G H	8777	615219	Hydrocephalus, congenital, 2, with or without brain or eye anomalies	615219	C3554691	OMIM	1	1610	7208	603785
HP:0001270	HP:0025336	Delayed ability to sit	2	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0032989	Delayed ability to roll over	2	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0033128	Delayed ability to crawl	2	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0031936	Delayed ability to walk	2	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0025335	Delayed ability to stand	2	MPZ CL E G H	4359	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	607	7225	159440
HP:0001270	HP:0033128	Delayed ability to crawl	2	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0031936	Delayed ability to walk	2	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0025335	Delayed ability to stand	2	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0025336	Delayed ability to sit	2	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0032989	Delayed ability to roll over	2	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MPZ CL E G H	4359	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	607	7225	159440
HP:0001270	HP:0025336	Delayed ability to sit	2	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0032989	Delayed ability to roll over	2	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0033128	Delayed ability to crawl	2	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0031936	Delayed ability to walk	2	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0025335	Delayed ability to stand	2	MSTO1 CL E G H	55154	502423				ORPHA	1	158	29678	617619
HP:0001270	HP:0025335	Delayed ability to stand	2	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0025336	Delayed ability to sit	2	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0032989	Delayed ability to roll over	2	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0033128	Delayed ability to crawl	2	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0031936	Delayed ability to walk	2	MSTO1 CL E G H	55154	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA	617675	C4540096	OMIM	1	158	29678	617619
HP:0001270	HP:0025336	Delayed ability to sit	2	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0032989	Delayed ability to roll over	2	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0033128	Delayed ability to crawl	2	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0031936	Delayed ability to walk	2	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0025335	Delayed ability to stand	2	MT-TN CL E G H	4570	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7493	590010
HP:0001270	HP:0033128	Delayed ability to crawl	2	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0031936	Delayed ability to walk	2	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0025335	Delayed ability to stand	2	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0025336	Delayed ability to sit	2	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0032989	Delayed ability to roll over	2	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MT-TS1 CL E G H	4574	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1		7497	590080
HP:0001270	HP:0031936	Delayed ability to walk	2	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0033128	Delayed ability to crawl	2	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0025335	Delayed ability to stand	2	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0025336	Delayed ability to sit	2	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0032989	Delayed ability to roll over	2	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MT-TW CL E G H	4578	251900	Mitochondrial myopathy	251900	C0162670	OMIM	1		7501	590095
HP:0001270	HP:0025335	Delayed ability to stand	2	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0025336	Delayed ability to sit	2	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0032989	Delayed ability to roll over	2	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0033128	Delayed ability to crawl	2	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0031936	Delayed ability to walk	2	MTMR2 CL E G H	8898	601382	Charcot-Marie-Tooth disease, type 4B1	601382	C1832399	OMIM	1	540	7450	603557
HP:0001270	HP:0033128	Delayed ability to crawl	2	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0031936	Delayed ability to walk	2	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0025335	Delayed ability to stand	2	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0025336	Delayed ability to sit	2	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0032989	Delayed ability to roll over	2	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MTPAP CL E G H	55149	254343				ORPHA	1	346	25532	613669
HP:0001270	HP:0025336	Delayed ability to sit	2	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0031936	Delayed ability to walk	2	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0025335	Delayed ability to stand	2	MYL2 CL E G H	4633	2020				ORPHA	1	496	7583	160781
HP:0001270	HP:0025336	Delayed ability to sit	2	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0031936	Delayed ability to walk	2	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0025335	Delayed ability to stand	2	MYMK CL E G H	389827	254940	Congenital nonprogressive myopathy with Moebius and Robin sequences	254940	C1850746	OMIM	1	86	33778	615345
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0031936	Delayed ability to walk	2	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0025335	Delayed ability to stand	2	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0025336	Delayed ability to sit	2	MYO7A CL E G H	4647	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	3599	7606	276903
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0031936	Delayed ability to walk	2	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0031936	Delayed ability to walk	2	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0025335	Delayed ability to stand	2	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0025335	Delayed ability to stand	2	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0025336	Delayed ability to sit	2	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0025336	Delayed ability to sit	2	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYPN CL E G H	84665	171439				ORPHA	1	1485	23246	608517
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYPN CL E G H	84665	171881				ORPHA	1	1485	23246	608517
HP:0001270	HP:0025335	Delayed ability to stand	2	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0025336	Delayed ability to sit	2	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0032989	Delayed ability to roll over	2	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0031936	Delayed ability to walk	2	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0033128	Delayed ability to crawl	2	NAA10 CL E G H	8260	309800	Lenz microphthalmia syndrome	309800	C0796016	OMIM	1	401	18704	300013
HP:0001270	HP:0025335	Delayed ability to stand	2	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0025336	Delayed ability to sit	2	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0032989	Delayed ability to roll over	2	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0033128	Delayed ability to crawl	2	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0031936	Delayed ability to walk	2	NAA15 CL E G H	80155	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50	617787	C4540470	OMIM	1	317	30782	608000
HP:0001270	HP:0025336	Delayed ability to sit	2	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0032989	Delayed ability to roll over	2	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0033128	Delayed ability to crawl	2	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0031936	Delayed ability to walk	2	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0025335	Delayed ability to stand	2	NDN CL E G H	4692	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	328	7675	602117
HP:0001270	HP:0025336	Delayed ability to sit	2	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0025335	Delayed ability to stand	2	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0031936	Delayed ability to walk	2	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0025336	Delayed ability to sit	2	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0031936	Delayed ability to walk	2	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0025335	Delayed ability to stand	2	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0025335	Delayed ability to stand	2	NEB CL E G H	4703	171439				ORPHA	1	8530	7720	161650
HP:0001270	HP:0031936	Delayed ability to walk	2	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0025336	Delayed ability to sit	2	NEB CL E G H	4703	171433				ORPHA	1	8530	7720	161650
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEB CL E G H	4703	171430				ORPHA	1	8530	7720	161650
HP:0001270	HP:0025336	Delayed ability to sit	2	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0031936	Delayed ability to walk	2	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0025335	Delayed ability to stand	2	NEB CL E G H	4703	256030	Nemaline myopathy 2	256030	C1850569	OMIM	1	8530	7720	161650
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0031936	Delayed ability to walk	2	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0025335	Delayed ability to stand	2	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0025336	Delayed ability to sit	2	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEFL CL E G H	4747	607734	Charcot-Marie-Tooth disease, demyelinating, type 1f	607734	C1843164	OMIM	1	614	7739	162280
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0031936	Delayed ability to walk	2	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0025335	Delayed ability to stand	2	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0025336	Delayed ability to sit	2	NEFL CL E G H	4747	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G	617882	CN847583	OMIM	1	614	7739	162280
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0032989	Delayed ability to roll over	2	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0033128	Delayed ability to crawl	2	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0031936	Delayed ability to walk	2	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0025335	Delayed ability to stand	2	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0025336	Delayed ability to sit	2	NFIX CL E G H	4784	602535	Marshall-Smith syndrome	602535	C0265211	OMIM	1	348	7788	164005
HP:0001270	HP:0025336	Delayed ability to sit	2	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0032989	Delayed ability to roll over	2	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0033128	Delayed ability to crawl	2	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0031936	Delayed ability to walk	2	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0025335	Delayed ability to stand	2	NFIX CL E G H	4784	614753	Sotos syndrome 2	614753	C3553660	OMIM	1	348	7788	164005
HP:0001270	HP:0031936	Delayed ability to walk	2	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0033128	Delayed ability to crawl	2	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0025335	Delayed ability to stand	2	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0025336	Delayed ability to sit	2	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0032989	Delayed ability to roll over	2	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NKX2-1 CL E G H	7080	118700	Benign hereditary chorea	118700	C0393584	OMIM	1	317	11825	600635
HP:0001270	HP:0031936	Delayed ability to walk	2	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0033128	Delayed ability to crawl	2	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0025335	Delayed ability to stand	2	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0025336	Delayed ability to sit	2	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0032989	Delayed ability to roll over	2	NKX2-1 CL E G H	7080	610978	Choreoathetosis, hypothyroidism, and neonatal respiratory distress	610978	C1970269	OMIM	1	317	11825	600635
HP:0001270	HP:0025335	Delayed ability to stand	2	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0025336	Delayed ability to sit	2	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0032989	Delayed ability to roll over	2	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0033128	Delayed ability to crawl	2	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0031936	Delayed ability to walk	2	NKX6-2 CL E G H	84504	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY	617560	C4479653	OMIM	1	233	19321	605955
HP:0001270	HP:0025335	Delayed ability to stand	2	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0025336	Delayed ability to sit	2	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0032989	Delayed ability to roll over	2	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0033128	Delayed ability to crawl	2	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0031936	Delayed ability to walk	2	NONO CL E G H	4841	300967	Mental retardation, X-linked, syndromic 34	300967	C4225417	OMIM	1	243	7871	300084
HP:0001270	HP:0025336	Delayed ability to sit	2	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0032989	Delayed ability to roll over	2	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0033128	Delayed ability to crawl	2	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0031936	Delayed ability to walk	2	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0025335	Delayed ability to stand	2	NOTCH3 CL E G H	4854	130720	Lehman syndrome	130720	C1851710	OMIM	1	1343	7883	600276
HP:0001270	HP:0031936	Delayed ability to walk	2	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0033128	Delayed ability to crawl	2	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0025335	Delayed ability to stand	2	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0025336	Delayed ability to sit	2	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0032989	Delayed ability to roll over	2	NPAP1 CL E G H	23742	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	387	1190	610922
HP:0001270	HP:0031936	Delayed ability to walk	2	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0033128	Delayed ability to crawl	2	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0025335	Delayed ability to stand	2	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0025336	Delayed ability to sit	2	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0032989	Delayed ability to roll over	2	NRAS CL E G H	4893	613224	Noonan syndrome 6	613224	C2750732	OMIM	1	281	7989	164790
HP:0001270	HP:0033128	Delayed ability to crawl	2	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0031936	Delayed ability to walk	2	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0025335	Delayed ability to stand	2	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0025336	Delayed ability to sit	2	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0032989	Delayed ability to roll over	2	NT5C2 CL E G H	22978	320396				ORPHA	1	230	8022	600417
HP:0001270	HP:0033128	Delayed ability to crawl	2	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0031936	Delayed ability to walk	2	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0025335	Delayed ability to stand	2	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0025336	Delayed ability to sit	2	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0032989	Delayed ability to roll over	2	NT5C2 CL E G H	22978	613162	Spastic paraplegia 45, autosomal recessive	613162	C3888209	OMIM	1	230	8022	600417
HP:0001270	HP:0025336	Delayed ability to sit	2	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0033257	Delayed ability to walk with support	2	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0032989	Delayed ability to roll over	2	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0031936	Delayed ability to walk	2	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0033128	Delayed ability to crawl	2	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0025335	Delayed ability to stand	2	OPA1 CL E G H	4976	210000	Abortive cerebellar ataxia	210000	C0221061	OMIM	1	1224	8140	605290
HP:0001270	HP:0032989	Delayed ability to roll over	2	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0033128	Delayed ability to crawl	2	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0031936	Delayed ability to walk	2	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0025335	Delayed ability to stand	2	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0025336	Delayed ability to sit	2	PBX1 CL E G H	5087	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY	617641	C4539968	OMIM	1	109	8632	176310
HP:0001270	HP:0025336	Delayed ability to sit	2	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0032989	Delayed ability to roll over	2	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0031936	Delayed ability to walk	2	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0033128	Delayed ability to crawl	2	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0025335	Delayed ability to stand	2	PCBD1 CL E G H	5092	264070	Hyperphenylalaninemia, BH4-deficient, D	264070	C1849700	OMIM	1	91	8646	126090
HP:0001270	HP:0032989	Delayed ability to roll over	2	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0033128	Delayed ability to crawl	2	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0031936	Delayed ability to walk	2	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0025335	Delayed ability to stand	2	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0025336	Delayed ability to sit	2	PCDH15 CL E G H	65217	602083	Usher syndrome, type 1F	602083	C1865885	OMIM	1	2917	14674	605514
HP:0001270	HP:0033128	Delayed ability to crawl	2	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0031936	Delayed ability to walk	2	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0025335	Delayed ability to stand	2	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0025336	Delayed ability to sit	2	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0032989	Delayed ability to roll over	2	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PDE10A CL E G H	10846	494526				ORPHA	1	222	8772	610652
HP:0001270	HP:0025335	Delayed ability to stand	2	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0025336	Delayed ability to sit	2	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0032989	Delayed ability to roll over	2	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0033128	Delayed ability to crawl	2	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0031936	Delayed ability to walk	2	PDE10A CL E G H	10846	616921	Dyskinesia, limb and orofacial, infantile-onset	616921	C4310792	OMIM	1	222	8772	610652
HP:0001270	HP:0025335	Delayed ability to stand	2	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0025336	Delayed ability to sit	2	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0032989	Delayed ability to roll over	2	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0033128	Delayed ability to crawl	2	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0031936	Delayed ability to walk	2	PDX1 CL E G H	3651	99885				ORPHA	1	170	6107	600733
HP:0001270	HP:0025336	Delayed ability to sit	2	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0032989	Delayed ability to roll over	2	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0033128	Delayed ability to crawl	2	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0031936	Delayed ability to walk	2	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0025335	Delayed ability to stand	2	PDX1 CL E G H	3651	606176	Permanent neonatal diabetes mellitus	606176	C1833104	OMIM	1	170	6107	600733
HP:0001270	HP:0033128	Delayed ability to crawl	2	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0031936	Delayed ability to walk	2	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0025335	Delayed ability to stand	2	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0025336	Delayed ability to sit	2	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0032989	Delayed ability to roll over	2	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PET100 CL E G H	100131801	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	76	40038	614770
HP:0001270	HP:0032989	Delayed ability to roll over	2	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0033128	Delayed ability to crawl	2	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0031936	Delayed ability to walk	2	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0025335	Delayed ability to stand	2	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0025336	Delayed ability to sit	2	PHKA2 CL E G H	5256	306000	Glycogen storage disease type IXa1	306000	C0017927	OMIM	1	596	8926	300798
HP:0001270	HP:0025336	Delayed ability to sit	2	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0032989	Delayed ability to roll over	2	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0031936	Delayed ability to walk	2	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0033128	Delayed ability to crawl	2	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0025335	Delayed ability to stand	2	PHKG2 CL E G H	5261	613027	Glycogen storage disease IXc	613027	C2751643	OMIM	1	216	8931	172471
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0032989	Delayed ability to roll over	2	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0031936	Delayed ability to walk	2	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0033128	Delayed ability to crawl	2	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0025335	Delayed ability to stand	2	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0025336	Delayed ability to sit	2	PLAGL1 CL E G H	5325	99886				ORPHA	1	48	9046	603044
HP:0001270	HP:0025336	Delayed ability to sit	2	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0032989	Delayed ability to roll over	2	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0033128	Delayed ability to crawl	2	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0031936	Delayed ability to walk	2	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0025335	Delayed ability to stand	2	PLEC CL E G H	5339	613723	Limb-girdle muscular dystrophy, type 2Q	613723	C3150989	OMIM	1	5068	9069	601282
HP:0001270	HP:0025336	Delayed ability to sit	2	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0032989	Delayed ability to roll over	2	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0033128	Delayed ability to crawl	2	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0031936	Delayed ability to walk	2	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0025335	Delayed ability to stand	2	PLOD1 CL E G H	5351	225400	Ehlers-Danlos syndrome, hydroxylysine-deficient	225400	C0268342	OMIM	1	931	9081	153454
HP:0001270	HP:0033128	Delayed ability to crawl	2	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0031936	Delayed ability to walk	2	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0025335	Delayed ability to stand	2	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0025336	Delayed ability to sit	2	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0032989	Delayed ability to roll over	2	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PLXND1 CL E G H	23129	570				ORPHA	1	214	9107	604282
HP:0001270	HP:0033128	Delayed ability to crawl	2	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0031936	Delayed ability to walk	2	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0025335	Delayed ability to stand	2	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0025336	Delayed ability to sit	2	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0032989	Delayed ability to roll over	2	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PMP22 CL E G H	5376	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	492	9118	601097
HP:0001270	HP:0025336	Delayed ability to sit	2	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0032989	Delayed ability to roll over	2	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0033128	Delayed ability to crawl	2	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0031936	Delayed ability to walk	2	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0025335	Delayed ability to stand	2	PMP22 CL E G H	5376	180800	Roussy-Lévy syndrome	180800	C0205713	OMIM	1	492	9118	601097
HP:0001270	HP:0031936	Delayed ability to walk	2	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0033128	Delayed ability to crawl	2	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0025335	Delayed ability to stand	2	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0025336	Delayed ability to sit	2	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0032989	Delayed ability to roll over	2	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PNKP CL E G H	11284	613402	Early infantile epileptic encephalopathy 10	613402	C3150667	OMIM	1	1028	9154	605610
HP:0001270	HP:0025336	Delayed ability to sit	2	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0032989	Delayed ability to roll over	2	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0033128	Delayed ability to crawl	2	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0031936	Delayed ability to walk	2	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0025335	Delayed ability to stand	2	PNP CL E G H	4860	613179	Purine-nucleoside phosphorylase deficiency	613179	C0268125	OMIM	1	258	7892	164050
HP:0001270	HP:0025335	Delayed ability to stand	2	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0025336	Delayed ability to sit	2	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0032989	Delayed ability to roll over	2	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0033128	Delayed ability to crawl	2	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0031936	Delayed ability to walk	2	PNPLA2 CL E G H	57104	98908				ORPHA	1	566	30802	609059
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0031936	Delayed ability to walk	2	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0025335	Delayed ability to stand	2	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0025336	Delayed ability to sit	2	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMGNT1 CL E G H	55624	613151	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3	613151	C3150412	OMIM	1	1174	19139	606822
HP:0001270	HP:0025335	Delayed ability to stand	2	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0025336	Delayed ability to sit	2	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0031936	Delayed ability to walk	2	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMK CL E G H	84197	616094	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12	616094	C4015184	OMIM	1	307	26267	615247
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0031936	Delayed ability to walk	2	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0025335	Delayed ability to stand	2	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0025336	Delayed ability to sit	2	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMT1 CL E G H	10585	370980				ORPHA	1	906	9202	607423
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0031936	Delayed ability to walk	2	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0025335	Delayed ability to stand	2	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0025336	Delayed ability to sit	2	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMT1 CL E G H	10585	609308	Limb-girdle muscular dystrophy-dystroglycanopathy, type C1	609308	C1836373	OMIM	1	906	9202	607423
HP:0001270	HP:0025336	Delayed ability to sit	2	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0031936	Delayed ability to walk	2	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0025335	Delayed ability to stand	2	POMT2 CL E G H	29954	613156	Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2	613156	C3150416	OMIM	1	936	19743	607439
HP:0001270	HP:0025336	Delayed ability to sit	2	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0031936	Delayed ability to walk	2	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0025335	Delayed ability to stand	2	POMT2 CL E G H	29954	613158	Limb-girdle muscular dystrophy-dystroglycanopathy, type C2	613158	C3150418	OMIM	1	936	19743	607439
HP:0001270	HP:0032989	Delayed ability to roll over	2	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0033128	Delayed ability to crawl	2	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0031936	Delayed ability to walk	2	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0025335	Delayed ability to stand	2	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0025336	Delayed ability to sit	2	PREPL CL E G H	9581	616224	Myasthenic syndrome, congenital, 22	616224	C4479088	OMIM	1	708	30228	609557
HP:0001270	HP:0033128	Delayed ability to crawl	2	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0031936	Delayed ability to walk	2	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0025335	Delayed ability to stand	2	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0025336	Delayed ability to sit	2	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0032989	Delayed ability to roll over	2	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PRKRA CL E G H	8575	612067	Dystonia 16	612067	C2677567	OMIM	1	192	9438	603424
HP:0001270	HP:0025335	Delayed ability to stand	2	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0025336	Delayed ability to sit	2	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0032989	Delayed ability to roll over	2	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0031936	Delayed ability to walk	2	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0033128	Delayed ability to crawl	2	PRPS1 CL E G H	5631	311070	Charcot-Marie-Tooth disease, X-linked recessive, type 5	311070	C1839566	OMIM	1	415	9462	311850
HP:0001270	HP:0032989	Delayed ability to roll over	2	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0033128	Delayed ability to crawl	2	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0031936	Delayed ability to walk	2	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0025335	Delayed ability to stand	2	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0025336	Delayed ability to sit	2	PRPS1 CL E G H	5631	300661	Phosphoribosylpyrophosphate synthetase superactivity	300661	C1970827	OMIM	1	415	9462	311850
HP:0001270	HP:0025336	Delayed ability to sit	2	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0032989	Delayed ability to roll over	2	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0033128	Delayed ability to crawl	2	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0031936	Delayed ability to walk	2	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0025335	Delayed ability to stand	2	PRX CL E G H	57716	614895	Charcot-Marie-Tooth disease, demyelinating, type 4f	614895	C3540453	OMIM	1	1243	13797	605725
HP:0001270	HP:0025336	Delayed ability to sit	2	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0032989	Delayed ability to roll over	2	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0033128	Delayed ability to crawl	2	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0031936	Delayed ability to walk	2	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0025335	Delayed ability to stand	2	PRX CL E G H	57716	145900	Dejerine-Sottas disease	145900	C0011195	OMIM	1	1243	13797	605725
HP:0001270	HP:0025336	Delayed ability to sit	2	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0032989	Delayed ability to roll over	2	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0033128	Delayed ability to crawl	2	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0031936	Delayed ability to walk	2	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0025335	Delayed ability to stand	2	PTCH1 CL E G H	5727	109400	Gorlin syndrome	109400	C0004779	OMIM	1	4487	9585	601309
HP:0001270	HP:0031936	Delayed ability to walk	2	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0033128	Delayed ability to crawl	2	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0025335	Delayed ability to stand	2	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0025336	Delayed ability to sit	2	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0032989	Delayed ability to roll over	2	PTCH2 CL E G H	8643	109400	Gorlin syndrome	109400	C0004779	OMIM	1	791	9586	603673
HP:0001270	HP:0025336	Delayed ability to sit	2	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0032989	Delayed ability to roll over	2	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0033128	Delayed ability to crawl	2	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0031936	Delayed ability to walk	2	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0025335	Delayed ability to stand	2	PTPRQ CL E G H	374462	613391	Deafness, autosomal recessive 84	613391	C3150654	OMIM	1	420	9679	603317
HP:0001270	HP:0033128	Delayed ability to crawl	2	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0031936	Delayed ability to walk	2	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0025335	Delayed ability to stand	2	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0025336	Delayed ability to sit	2	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0032989	Delayed ability to roll over	2	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PUM1 CL E G H	9698	617931	SPINOCEREBELLAR ATAXIA 47	617931	CN244564	OMIM	1	175	14957	607204
HP:0001270	HP:0025336	Delayed ability to sit	2	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0032989	Delayed ability to roll over	2	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0033128	Delayed ability to crawl	2	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0031936	Delayed ability to walk	2	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0025335	Delayed ability to stand	2	PWAR1 CL E G H	145624	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	303	30089	600161
HP:0001270	HP:0031936	Delayed ability to walk	2	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0033128	Delayed ability to crawl	2	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0025335	Delayed ability to stand	2	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0025336	Delayed ability to sit	2	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0032989	Delayed ability to roll over	2	PWRN1 CL E G H	791114	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	314	33235	611215
HP:0001270	HP:0025335	Delayed ability to stand	2	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0025336	Delayed ability to sit	2	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0032989	Delayed ability to roll over	2	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0033128	Delayed ability to crawl	2	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0031936	Delayed ability to walk	2	RBM8A CL E G H	9939	274000	Radial aplasia-thrombocytopenia syndrome	274000	C0175703	OMIM	1	252	9905	605313
HP:0001270	HP:0025336	Delayed ability to sit	2	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0033257	Delayed ability to walk with support	2	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0032989	Delayed ability to roll over	2	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0033128	Delayed ability to crawl	2	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0031936	Delayed ability to walk	2	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0025335	Delayed ability to stand	2	REV3L CL E G H	5980	570				ORPHA	1	212	9968	602776
HP:0001270	HP:0025336	Delayed ability to sit	2	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0032989	Delayed ability to roll over	2	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0033128	Delayed ability to crawl	2	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0031936	Delayed ability to walk	2	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0025335	Delayed ability to stand	2	RORA CL E G H	6095	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA	618060	CN252646	OMIM	1	138	10258	600825
HP:0001270	HP:0032989	Delayed ability to roll over	2	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0033128	Delayed ability to crawl	2	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0031936	Delayed ability to walk	2	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0025335	Delayed ability to stand	2	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0025336	Delayed ability to sit	2	RPS23 CL E G H	6228	617412	MacInnes syndrome	617412	C4479431	OMIM	1	18	10410	603683
HP:0001270	HP:0032989	Delayed ability to roll over	2	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0033128	Delayed ability to crawl	2	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0031936	Delayed ability to walk	2	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0025335	Delayed ability to stand	2	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0025336	Delayed ability to sit	2	RPS6KA3 CL E G H	6197	300844	Mental retardation, X-linked 19	300844	C0796225	OMIM	1	515	10432	300075
HP:0001270	HP:0025335	Delayed ability to stand	2	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0025336	Delayed ability to sit	2	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0032989	Delayed ability to roll over	2	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0033128	Delayed ability to crawl	2	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0031936	Delayed ability to walk	2	RSPRY1 CL E G H	89970	616723	Spondyloepimetaphyseal dysplasia, Faden-Alkuraya type	616723	C4225232	OMIM	1	139	29420	616585
HP:0001270	HP:0033128	Delayed ability to crawl	2	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0031936	Delayed ability to walk	2	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0025335	Delayed ability to stand	2	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0025336	Delayed ability to sit	2	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0032989	Delayed ability to roll over	2	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RUBCN CL E G H	9711	615705	Spinocerebellar ataxia, autosomal recessive 15	615705	C3810326	OMIM	1	162	28991	613516
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	597				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	324581				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	424107				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	98905				ORPHA	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	169186				ORPHA	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	117000	117000	117000		OMIM	1	6164	10483	180901
HP:0001270	HP:0025336	Delayed ability to sit	2	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0033257	Delayed ability to walk with support	2	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0033128	Delayed ability to crawl	2	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0031936	Delayed ability to walk	2	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0025335	Delayed ability to stand	2	RYR1 CL E G H	6261	255320	Minicore myopathy	255320	C1850674	OMIM	1	6164	10483	180901
HP:0001270	HP:0032989	Delayed ability to roll over	2	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0033128	Delayed ability to crawl	2	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0031936	Delayed ability to walk	2	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0025335	Delayed ability to stand	2	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0025336	Delayed ability to sit	2	SAMD9 CL E G H	54809	617053	Mirage syndrome	617053	C4284088	OMIM	1	748	1348	610456
HP:0001270	HP:0025336	Delayed ability to sit	2	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0032989	Delayed ability to roll over	2	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0033128	Delayed ability to crawl	2	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0031936	Delayed ability to walk	2	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0025335	Delayed ability to stand	2	SCN11A CL E G H	11280	615548	Neuropathy, hereditary sensory and autonomic, type VII	615548	C3809882	OMIM	1	1212	10583	604385
HP:0001270	HP:0025336	Delayed ability to sit	2	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0032989	Delayed ability to roll over	2	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0033128	Delayed ability to crawl	2	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0031936	Delayed ability to walk	2	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0025335	Delayed ability to stand	2	SCN1A CL E G H	6323	607208	Severe myoclonic epilepsy in infancy	607208	C0751122	OMIM	1	4030	10585	182389
HP:0001270	HP:0025336	Delayed ability to sit	2	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0032989	Delayed ability to roll over	2	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0031936	Delayed ability to walk	2	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0033128	Delayed ability to crawl	2	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0025335	Delayed ability to stand	2	SCN4A CL E G H	6329	614198	Congenital myasthenic syndrome, acetazolamide-responsive	614198	C3502630	OMIM	1	1765	10591	603967
HP:0001270	HP:0025336	Delayed ability to sit	2	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0032989	Delayed ability to roll over	2	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0033128	Delayed ability to crawl	2	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0031936	Delayed ability to walk	2	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0025335	Delayed ability to stand	2	SCO1 CL E G H	6341	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	212	10603	603644
HP:0001270	HP:0033128	Delayed ability to crawl	2	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0031936	Delayed ability to walk	2	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0025335	Delayed ability to stand	2	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0025336	Delayed ability to sit	2	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0032989	Delayed ability to roll over	2	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SCO2 CL E G H	9997	521411				ORPHA	1	701	10604	604272
HP:0001270	HP:0025335	Delayed ability to stand	2	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0025336	Delayed ability to sit	2	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0032989	Delayed ability to roll over	2	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0033128	Delayed ability to crawl	2	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0031936	Delayed ability to walk	2	SCYL1 CL E G H	57410	616719	Spinocerebellar ataxia, autosomal recessive 21	616719	C4225236	OMIM	1	128	14372	607982
HP:0001270	HP:0025336	Delayed ability to sit	2	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0032989	Delayed ability to roll over	2	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0033128	Delayed ability to crawl	2	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0031936	Delayed ability to walk	2	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0025335	Delayed ability to stand	2	SDHA CL E G H	6389	3208				ORPHA	1	2503	10680	600857
HP:0001270	HP:0031936	Delayed ability to walk	2	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0033128	Delayed ability to crawl	2	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0025335	Delayed ability to stand	2	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0025336	Delayed ability to sit	2	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0032989	Delayed ability to roll over	2	SDHAF1 CL E G H	644096	3208				ORPHA	1	77	33867	612848
HP:0001270	HP:0025336	Delayed ability to sit	2	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0032989	Delayed ability to roll over	2	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0033128	Delayed ability to crawl	2	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0031936	Delayed ability to walk	2	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0025335	Delayed ability to stand	2	SDHB CL E G H	6390	3208				ORPHA	1	1249	10681	185470
HP:0001270	HP:0031936	Delayed ability to walk	2	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0033128	Delayed ability to crawl	2	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0025335	Delayed ability to stand	2	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0025336	Delayed ability to sit	2	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0032989	Delayed ability to roll over	2	SDHD CL E G H	6392	3208				ORPHA	1	686	10683	602690
HP:0001270	HP:0033128	Delayed ability to crawl	2	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0031936	Delayed ability to walk	2	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0025335	Delayed ability to stand	2	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0025336	Delayed ability to sit	2	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0032989	Delayed ability to roll over	2	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SELENON CL E G H	57190	2020				ORPHA	1	651	15999	606210
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0032989	Delayed ability to roll over	2	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0031936	Delayed ability to walk	2	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0033128	Delayed ability to crawl	2	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0025335	Delayed ability to stand	2	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0025336	Delayed ability to sit	2	SELENON CL E G H	57190	602771	Eichsfeld type congenital muscular dystrophy	602771	C0410180	OMIM	1	651	15999	606210
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0033128	Delayed ability to crawl	2	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0031936	Delayed ability to walk	2	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0025335	Delayed ability to stand	2	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0025336	Delayed ability to sit	2	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0032989	Delayed ability to roll over	2	SETBP1 CL E G H	26040	616078	Mental retardation, autosomal dominant 29	616078	C4015141	OMIM	1	1190	15573	611060
HP:0001270	HP:0032989	Delayed ability to roll over	2	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0033128	Delayed ability to crawl	2	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0031936	Delayed ability to walk	2	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0025335	Delayed ability to stand	2	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0025336	Delayed ability to sit	2	SH3TC2 CL E G H	79628	601596	Charcot-Marie-Tooth disease, type 4C	601596	C1866636	OMIM	1	1674	29427	608206
HP:0001270	HP:0031936	Delayed ability to walk	2	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0033128	Delayed ability to crawl	2	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0025335	Delayed ability to stand	2	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0025336	Delayed ability to sit	2	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0032989	Delayed ability to roll over	2	SHANK3 CL E G H	85358	606232	22q13.3 deletion syndrome	606232	C1853490	OMIM	1	936	14294	606230
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC12A6 CL E G H	9990	218000	Andermann syndrome	218000	C0795950	OMIM	1	1185	10914	604878
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC1A3 CL E G H	6507	612656	Episodic ataxia, type 6	612656	C2675211	OMIM	1	266	10941	600111
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC6A8 CL E G H	6535	300352	Creatine deficiency, X-linked	300352	C1845862	OMIM	1	1062	11055	300036
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC9A1 CL E G H	6548	616291	Lichtenstein-knorr syndrome	616291	C4225383	OMIM	1	162	11071	107310
HP:0001270	HP:0033128	Delayed ability to crawl	2	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0031936	Delayed ability to walk	2	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0025335	Delayed ability to stand	2	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0025336	Delayed ability to sit	2	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0032989	Delayed ability to roll over	2	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SMARCAL1 CL E G H	50485	242900	Schimke immunoosseous dysplasia	242900	C0877024	OMIM	1	942	11102	606622
HP:0001270	HP:0025336	Delayed ability to sit	2	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0032989	Delayed ability to roll over	2	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0033128	Delayed ability to crawl	2	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0031936	Delayed ability to walk	2	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0025335	Delayed ability to stand	2	SNORD115-1 CL E G H	338433	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33020	609837
HP:0001270	HP:0031936	Delayed ability to walk	2	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0033128	Delayed ability to crawl	2	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0025335	Delayed ability to stand	2	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0025336	Delayed ability to sit	2	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0032989	Delayed ability to roll over	2	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SNORD116-1 CL E G H	100033413	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	305	33067	605436
HP:0001270	HP:0025336	Delayed ability to sit	2	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0032989	Delayed ability to roll over	2	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0033128	Delayed ability to crawl	2	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0031936	Delayed ability to walk	2	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0025335	Delayed ability to stand	2	SNRPN CL E G H	6638	176270	Prader-Willi syndrome	176270	C0032897	OMIM	1	396	11164	182279
HP:0001270	HP:0033128	Delayed ability to crawl	2	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0031936	Delayed ability to walk	2	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0025335	Delayed ability to stand	2	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0025336	Delayed ability to sit	2	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0032989	Delayed ability to roll over	2	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SOX5 CL E G H	6660	313892				ORPHA	1	264	11201	604975
HP:0001270	HP:0025336	Delayed ability to sit	2	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0032989	Delayed ability to roll over	2	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0033128	Delayed ability to crawl	2	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0031936	Delayed ability to walk	2	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0025335	Delayed ability to stand	2	SP7 CL E G H	121340	613849	Osteogenesis imperfecta type 12	613849	C3151433	OMIM	1	132	17321	606633
HP:0001270	HP:0025335	Delayed ability to stand	2	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0025336	Delayed ability to sit	2	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0031936	Delayed ability to walk	2	SPARC CL E G H	6678	616507	Osteogenesis imperfecta, type xvii	616507	C4225301	OMIM	1	168	11219	182120
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0031936	Delayed ability to walk	2	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0025335	Delayed ability to stand	2	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0025336	Delayed ability to sit	2	SPART CL E G H	23111	101000				ORPHA	1	353	18514	607111
HP:0001270	HP:0025335	Delayed ability to stand	2	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0025336	Delayed ability to sit	2	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0031936	Delayed ability to walk	2	SPART CL E G H	23111	275900	Troyer syndrome	275900	C0393559	OMIM	1	353	18514	607111
HP:0001270	HP:0025335	Delayed ability to stand	2	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0025336	Delayed ability to sit	2	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0031936	Delayed ability to walk	2	SPEG CL E G H	10290	169186				ORPHA	1	1482	16901	615950
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0031936	Delayed ability to walk	2	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0025335	Delayed ability to stand	2	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0025336	Delayed ability to sit	2	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPEG CL E G H	10290	615959	Myopathy, centronuclear, 5	615959	C4014814	OMIM	1	1482	16901	615950
HP:0001270	HP:0025336	Delayed ability to sit	2	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0031936	Delayed ability to walk	2	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0025335	Delayed ability to stand	2	SPR CL E G H	6697	70594				ORPHA	1	198	11257	182125
HP:0001270	HP:0033128	Delayed ability to crawl	2	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0031936	Delayed ability to walk	2	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0025335	Delayed ability to stand	2	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0025336	Delayed ability to sit	2	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0032989	Delayed ability to roll over	2	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SRD5A3 CL E G H	79644	612379	Congenital disorder of glycosylation type 1Q	612379	C3150191	OMIM	1	236	25812	611715
HP:0001270	HP:0033128	Delayed ability to crawl	2	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0031936	Delayed ability to walk	2	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0025335	Delayed ability to stand	2	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0025336	Delayed ability to sit	2	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0032989	Delayed ability to roll over	2	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SRD5A3 CL E G H	79644	612713	Kahrizi syndrome	612713	C2675185	OMIM	1	236	25812	611715
HP:0001270	HP:0033128	Delayed ability to crawl	2	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0031936	Delayed ability to walk	2	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0025335	Delayed ability to stand	2	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0025336	Delayed ability to sit	2	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0032989	Delayed ability to roll over	2	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0033257	Delayed ability to walk with support	2	STAC3 CL E G H	246329	255995	Native American myopathy	255995	C1850625	OMIM	1	236	28423	615521
HP:0001270	HP:0032989	Delayed ability to roll over	2	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0033257	Delayed ability to walk with support	2	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0033128	Delayed ability to crawl	2	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0031936	Delayed ability to walk	2	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0025335	Delayed ability to stand	2	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0025336	Delayed ability to sit	2	STAT3 CL E G H	6774	99885				ORPHA	1	639	11364	102582
HP:0001270	HP:0025336	Delayed ability to sit	2	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0032989	Delayed ability to roll over	2	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0033128	Delayed ability to crawl	2	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0031936	Delayed ability to walk	2	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0025335	Delayed ability to stand	2	SUFU CL E G H	51684	109400	Gorlin syndrome	109400	C0004779	OMIM	1	1306	16466	607035
HP:0001270	HP:0033128	Delayed ability to crawl	2	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0031936	Delayed ability to walk	2	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0025335	Delayed ability to stand	2	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0025336	Delayed ability to sit	2	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0032989	Delayed ability to roll over	2	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SYNGAP1 CL E G H	8831	612621	Mental retardation, autosomal dominant 5	612621	C2675473	OMIM	1	1335	11497	603384
HP:0001270	HP:0033128	Delayed ability to crawl	2	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0031936	Delayed ability to walk	2	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0025335	Delayed ability to stand	2	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0025336	Delayed ability to sit	2	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0032989	Delayed ability to roll over	2	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TACO1 CL E G H	51204	220110	Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency	220110	C0268237	OMIM	1	117	24316	612958
HP:0001270	HP:0032989	Delayed ability to roll over	2	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0033128	Delayed ability to crawl	2	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0031936	Delayed ability to walk	2	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0025335	Delayed ability to stand	2	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0025336	Delayed ability to sit	2	TAZ CL E G H	6901	302060	3-Methylglutaconic aciduria type 2	302060	C0574083	OMIM	1		11577	300394
HP:0001270	HP:0025336	Delayed ability to sit	2	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0032989	Delayed ability to roll over	2	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0033128	Delayed ability to crawl	2	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0031936	Delayed ability to walk	2	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0025335	Delayed ability to stand	2	TCF4 CL E G H	6925	610954	Pitt-Hopkins syndrome	610954	C1970431	OMIM	1	1069	11634	602272
HP:0001270	HP:0025336	Delayed ability to sit	2	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0032989	Delayed ability to roll over	2	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0033128	Delayed ability to crawl	2	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0031936	Delayed ability to walk	2	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0025335	Delayed ability to stand	2	TENT5A CL E G H	55603	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII	617952	CN244563	OMIM	1	129	18345	611357
HP:0001270	HP:0032989	Delayed ability to roll over	2	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0033128	Delayed ability to crawl	2	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0031936	Delayed ability to walk	2	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0025335	Delayed ability to stand	2	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0025336	Delayed ability to sit	2	TH CL E G H	7054	101150				ORPHA	1	967	11782	191290
HP:0001270	HP:0025335	Delayed ability to stand	2	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0025336	Delayed ability to sit	2	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0032989	Delayed ability to roll over	2	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0033128	Delayed ability to crawl	2	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0031936	Delayed ability to walk	2	TH CL E G H	7054	605407	Segawa syndrome, autosomal recessive	605407	C1854299	OMIM	1	967	11782	191290
HP:0001270	HP:0025336	Delayed ability to sit	2	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0032989	Delayed ability to roll over	2	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0031936	Delayed ability to walk	2	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0033128	Delayed ability to crawl	2	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0025335	Delayed ability to stand	2	TK2 CL E G H	7084	254875				ORPHA	1	442	11831	188250
HP:0001270	HP:0033128	Delayed ability to crawl	2	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0031936	Delayed ability to walk	2	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0025335	Delayed ability to stand	2	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0025336	Delayed ability to sit	2	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0032989	Delayed ability to roll over	2	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TLK2 CL E G H	11011	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57	618050	CN252334	OMIM	1	170	11842	608439
HP:0001270	HP:0025336	Delayed ability to sit	2	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0032989	Delayed ability to roll over	2	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0031936	Delayed ability to walk	2	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0033128	Delayed ability to crawl	2	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0025335	Delayed ability to stand	2	TMCO1 CL E G H	54499	213980	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	213980	C1859252	OMIM	1	75	18188	614123
HP:0001270	HP:0025336	Delayed ability to sit	2	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0032989	Delayed ability to roll over	2	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0033128	Delayed ability to crawl	2	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0031936	Delayed ability to walk	2	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0025335	Delayed ability to stand	2	TNFRSF11A CL E G H	8792	612301	Osteopetrosis autosomal recessive 7	612301	C2676766	OMIM	1	572	11908	603499
HP:0001270	HP:0025335	Delayed ability to stand	2	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0025336	Delayed ability to sit	2	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0032989	Delayed ability to roll over	2	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0033128	Delayed ability to crawl	2	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0031936	Delayed ability to walk	2	TNNT1 CL E G H	7138	98902				ORPHA	1	372	11948	191041
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM2 CL E G H	7169	2020				ORPHA	1	341	12011	190990
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM2 CL E G H	7169	171881				ORPHA	1	341	12011	190990
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM2 CL E G H	7169	171439				ORPHA	1	341	12011	190990
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM2 CL E G H	7169	609285	Nemaline myopathy 4	609285	C1836447	OMIM	1	341	12011	190990
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM3 CL E G H	7170	2020				ORPHA	1	343	12012	191030
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM3 CL E G H	7170	171881				ORPHA	1	343	12012	191030
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM3 CL E G H	7170	171439				ORPHA	1	343	12012	191030
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM3 CL E G H	7170	171433				ORPHA	1	343	12012	191030
HP:0001270	HP:0033128	Delayed ability to crawl	2	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0031936	Delayed ability to walk	2	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0025335	Delayed ability to stand	2	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0025336	Delayed ability to sit	2	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0032989	Delayed ability to roll over	2	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TPM3 CL E G H	7170	609284	Nemaline myopathy 1	609284	C1836448	OMIM	1	343	12012	191030
HP:0001270	HP:0025335	Delayed ability to stand	2	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0025336	Delayed ability to sit	2	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0031936	Delayed ability to walk	2	TRIO CL E G H	7204	617061	Mental retardation, autosomal dominant 44	617061	C4310740	OMIM	1	1276	12303	601893
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0031936	Delayed ability to walk	2	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0025335	Delayed ability to stand	2	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0025336	Delayed ability to sit	2	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRIP11 CL E G H	9321	184260	Goldblatt hypertension	184260	C0018036	OMIM	1	774	12305	604505
HP:0001270	HP:0025336	Delayed ability to sit	2	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0031936	Delayed ability to walk	2	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0025335	Delayed ability to stand	2	TRIP4 CL E G H	9325	486815				ORPHA	1	212	12310	604501
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0031936	Delayed ability to walk	2	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0025335	Delayed ability to stand	2	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0025336	Delayed ability to sit	2	TRIP4 CL E G H	9325	617066	Muscular dystrophy, congenital, davignon-chauveau type	617066	C4310736	OMIM	1	212	12310	604501
HP:0001270	HP:0025336	Delayed ability to sit	2	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0031936	Delayed ability to walk	2	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0025335	Delayed ability to stand	2	TRMT10A CL E G H	93587	616033	Microcephaly, short stature, and impaired glucose metabolism 1	616033	C4014997	OMIM	1	133	28403	616013
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0031936	Delayed ability to walk	2	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0025335	Delayed ability to stand	2	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0025336	Delayed ability to sit	2	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRPV4 CL E G H	59341	181405	Scapuloperoneal spinal muscular atrophy	181405	C0751335	OMIM	1	1018	18083	605427
HP:0001270	HP:0025336	Delayed ability to sit	2	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0032989	Delayed ability to roll over	2	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0033128	Delayed ability to crawl	2	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0031936	Delayed ability to walk	2	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0025335	Delayed ability to stand	2	TRPV6 CL E G H	55503	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL	618188		OMIM	1	110	14006	606680
HP:0001270	HP:0025336	Delayed ability to sit	2	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0032989	Delayed ability to roll over	2	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0032989	Delayed ability to roll over	2	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0033128	Delayed ability to crawl	2	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0031936	Delayed ability to walk	2	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0033128	Delayed ability to crawl	2	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0031936	Delayed ability to walk	2	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0025335	Delayed ability to stand	2	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0025335	Delayed ability to stand	2	TSHR CL E G H	7253	424				ORPHA	1	249	12373	603372
HP:0001270	HP:0025336	Delayed ability to sit	2	TSHR CL E G H	7253	99819				ORPHA	1	249	12373	603372
HP:0001270	HP:0025336	Delayed ability to sit	2	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0032989	Delayed ability to roll over	2	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0033128	Delayed ability to crawl	2	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0031936	Delayed ability to walk	2	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0025335	Delayed ability to stand	2	TSHR CL E G H	7253	609152	Hyperthyroidism, nonautoimmune	609152	C1836706	OMIM	1	249	12373	603372
HP:0001270	HP:0032989	Delayed ability to roll over	2	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0033128	Delayed ability to crawl	2	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0031936	Delayed ability to walk	2	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0025335	Delayed ability to stand	2	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0025336	Delayed ability to sit	2	TTN CL E G H	7273	169186				ORPHA	1	27503	12403	188840
HP:0001270	HP:0025336	Delayed ability to sit	2	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0032989	Delayed ability to roll over	2	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0033128	Delayed ability to crawl	2	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0031936	Delayed ability to walk	2	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0025335	Delayed ability to stand	2	TTN CL E G H	7273	611705	Myopathy, early-onset, with fatal cardiomyopathy	611705	C2673677	OMIM	1	27503	12403	188840
HP:0001270	HP:0033128	Delayed ability to crawl	2	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0031936	Delayed ability to walk	2	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0025335	Delayed ability to stand	2	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0025336	Delayed ability to sit	2	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0032989	Delayed ability to roll over	2	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TUBA1A CL E G H	7846	611603	Lissencephaly 3	611603	C1969029	OMIM	1	325	20766	602529
HP:0001270	HP:0033128	Delayed ability to crawl	2	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0031936	Delayed ability to walk	2	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0025335	Delayed ability to stand	2	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0025336	Delayed ability to sit	2	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0032989	Delayed ability to roll over	2	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TUBB CL E G H	203068	156610	Michelin-tire baby	156610	C0473586	OMIM	1	94	20778	191130
HP:0001270	HP:0031936	Delayed ability to walk	2	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0033128	Delayed ability to crawl	2	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0025335	Delayed ability to stand	2	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0025336	Delayed ability to sit	2	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0032989	Delayed ability to roll over	2	TUBB2B CL E G H	347733	610031	Polymicrogyria, asymmetric	610031	C2750247	OMIM	1	204	30829	612850
HP:0001270	HP:0025336	Delayed ability to sit	2	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0032989	Delayed ability to roll over	2	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0033128	Delayed ability to crawl	2	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0031936	Delayed ability to walk	2	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0025335	Delayed ability to stand	2	TUBB4A CL E G H	10382	612438	Leukodystrophy, hypomyelinating, 6	612438	C2676244	OMIM	1	272	20774	602662
HP:0001270	HP:0033128	Delayed ability to crawl	2	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0031936	Delayed ability to walk	2	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0025335	Delayed ability to stand	2	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0025336	Delayed ability to sit	2	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0033257	Delayed ability to walk with support	2	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0032989	Delayed ability to roll over	2	UBE3A CL E G H	7337	105830	Angelman syndrome	105830	C0162635	OMIM	1	1108	12496	601623
HP:0001270	HP:0025335	Delayed ability to stand	2	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0025336	Delayed ability to sit	2	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0032989	Delayed ability to roll over	2	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0033257	Delayed ability to walk with support	2	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0033128	Delayed ability to crawl	2	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0031936	Delayed ability to walk	2	USH1C CL E G H	10083	276900	Usher syndrome, type 1	276900	C1568247	OMIM	1	1146	12597	605242
HP:0001270	HP:0032989	Delayed ability to roll over	2	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0033257	Delayed ability to walk with support	2	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0033128	Delayed ability to crawl	2	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0031936	Delayed ability to walk	2	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0025335	Delayed ability to stand	2	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0025336	Delayed ability to sit	2	VDR CL E G H	7421	277440	Vitamin D-dependent rickets, type 2	277440	C0342646	OMIM	1	345	12679	601769
HP:0001270	HP:0025336	Delayed ability to sit	2	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0033257	Delayed ability to walk with support	2	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0032989	Delayed ability to roll over	2	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0031936	Delayed ability to walk	2	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0033128	Delayed ability to crawl	2	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0025335	Delayed ability to stand	2	VPS13B CL E G H	157680	216550	Cohen syndrome	216550	C0265223	OMIM	1	4876	2183	607817
HP:0001270	HP:0033128	Delayed ability to crawl	2	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0031936	Delayed ability to walk	2	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0025335	Delayed ability to stand	2	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0025336	Delayed ability to sit	2	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0032989	Delayed ability to roll over	2	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0033257	Delayed ability to walk with support	2	WDR73 CL E G H	84942	83472				ORPHA	1	220	25928	616144
HP:0001270	HP:0025336	Delayed ability to sit	2	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0032989	Delayed ability to roll over	2	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0033257	Delayed ability to walk with support	2	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0033128	Delayed ability to crawl	2	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0031936	Delayed ability to walk	2	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0025335	Delayed ability to stand	2	WWOX CL E G H	51741	284282				ORPHA	1	1102	12799	605131
HP:0001270	HP:0033128	Delayed ability to crawl	2	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0031936	Delayed ability to walk	2	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0025335	Delayed ability to stand	2	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0025336	Delayed ability to sit	2	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0032989	Delayed ability to roll over	2	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ZBTB24 CL E G H	9841	614069	Immunodeficiency-centromeric instability-facial anomalies syndrome 2	614069	C3279748	OMIM	1	334	21143	614064
HP:0001270	HP:0025336	Delayed ability to sit	2	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0032989	Delayed ability to roll over	2	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0031936	Delayed ability to walk	2	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0033128	Delayed ability to crawl	2	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0025335	Delayed ability to stand	2	ZEB2 CL E G H	9839	235730	Mowat-Wilson syndrome	235730	C1856113	OMIM	1	1206	14881	605802
HP:0001270	HP:0025335	Delayed ability to stand	2	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0025336	Delayed ability to sit	2	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0032989	Delayed ability to roll over	2	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0033128	Delayed ability to crawl	2	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0031936	Delayed ability to walk	2	ZFP57 CL E G H	346171	99886				ORPHA	1	112	18791	612192
HP:0001270	HP:0025336	Delayed ability to sit	2	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0032989	Delayed ability to roll over	2	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0033128	Delayed ability to crawl	2	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0031936	Delayed ability to walk	2	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0025335	Delayed ability to stand	2	ZNF592 CL E G H	9640	83472				ORPHA	1	128	28986	613624
HP:0001270	HP:0025335	Delayed ability to stand	2	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0025336	Delayed ability to sit	2	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0032989	Delayed ability to roll over	2	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0033128	Delayed ability to crawl	2	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HP:0001270	HP:0031936	Delayed ability to walk	2	ZNF711 CL E G H	7552	300803	ZNF711-Related X-linked Mental Retardation	300803	C2749020	OMIM	1	282	13128	314990
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001270	HP:0001270	Motor delay	0	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0001270	Motor delay	0	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0001270	Motor delay	0	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0001270	Motor delay	0	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0001270	Motor delay	0	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0001270	Motor delay	0	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0001270	Motor delay	0	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0001270	Motor delay	0	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0001270	Motor delay	0	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0001270	Motor delay	0	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0001270	Motor delay	0	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0001270	Motor delay	0	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0001270	Motor delay	0	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0001270	Motor delay	0	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0001270	Motor delay	0	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0001270	Motor delay	0	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0001270	Motor delay	0	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0001270	Motor delay	0	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0001270	Motor delay	0	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0001270	Motor delay	0	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0001270	Motor delay	0	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0001270	Motor delay	0	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0001270	Motor delay	0	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0001270	Motor delay	0	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0001270	Motor delay	0	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0001270	Motor delay	0	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0001270	Motor delay	0	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0001270	Motor delay	0	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0001270	Motor delay	0	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0001270	Motor delay	0	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0001270	Motor delay	0	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0001270	Motor delay	0	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0001270	Motor delay	0	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0001270	Motor delay	0	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0001270	Motor delay	0	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0001270	Motor delay	0	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0001270	Motor delay	0	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0001270	Motor delay	0	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0001270	Motor delay	0	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0001270	Motor delay	0	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0001270	Motor delay	0	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0001270	Motor delay	0	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0001270	Motor delay	0	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0001270	Motor delay	0	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0001270	Motor delay	0	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0001270	Motor delay	0	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0001270	Motor delay	0	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0001270	Motor delay	0	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0001270	Motor delay	0	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0001270	Motor delay	0	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0001270	Motor delay	0	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0001270	Motor delay	0	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0001270	Motor delay	0	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0001270	Motor delay	0	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0001270	Motor delay	0	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0001270	Motor delay	0	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0001270	Motor delay	0	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0001270	Motor delay	0	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0001270	Motor delay	0	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0001270	Motor delay	0	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0010862	Delayed fine motor development	1	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0032988	Persistent head lag	1	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0002194	Delayed gross motor development	1	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0002194	Delayed gross motor development	1	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0032988	Persistent head lag	1	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0010862	Delayed fine motor development	1	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0002194	Delayed gross motor development	1	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0032988	Persistent head lag	1	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0010862	Delayed fine motor development	1	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0002194	Delayed gross motor development	1	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0010862	Delayed fine motor development	1	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0032988	Persistent head lag	1	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0002194	Delayed gross motor development	1	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0010862	Delayed fine motor development	1	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0032988	Persistent head lag	1	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0002194	Delayed gross motor development	1	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0010862	Delayed fine motor development	1	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0032988	Persistent head lag	1	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0002194	Delayed gross motor development	1	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0010862	Delayed fine motor development	1	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0032988	Persistent head lag	1	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0002194	Delayed gross motor development	1	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0010862	Delayed fine motor development	1	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0032988	Persistent head lag	1	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0010862	Delayed fine motor development	1	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0032988	Persistent head lag	1	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0002194	Delayed gross motor development	1	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0002194	Delayed gross motor development	1	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0010862	Delayed fine motor development	1	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0032988	Persistent head lag	1	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0002194	Delayed gross motor development	1	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0032988	Persistent head lag	1	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0010862	Delayed fine motor development	1	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0002194	Delayed gross motor development	1	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0010862	Delayed fine motor development	1	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0032988	Persistent head lag	1	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0002194	Delayed gross motor development	1	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0032988	Persistent head lag	1	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0010862	Delayed fine motor development	1	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0010862	Delayed fine motor development	1	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0032988	Persistent head lag	1	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0002194	Delayed gross motor development	1	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0002194	Delayed gross motor development	1	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0032988	Persistent head lag	1	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0010862	Delayed fine motor development	1	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0002194	Delayed gross motor development	1	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0032988	Persistent head lag	1	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0010862	Delayed fine motor development	1	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0002194	Delayed gross motor development	1	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0010862	Delayed fine motor development	1	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0032988	Persistent head lag	1	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0002194	Delayed gross motor development	1	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0032988	Persistent head lag	1	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0010862	Delayed fine motor development	1	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0002194	Delayed gross motor development	1	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0032988	Persistent head lag	1	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0010862	Delayed fine motor development	1	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0002194	Delayed gross motor development	1	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0010862	Delayed fine motor development	1	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0032988	Persistent head lag	1	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0032988	Persistent head lag	1	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0010862	Delayed fine motor development	1	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0002194	Delayed gross motor development	1	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0002194	Delayed gross motor development	1	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0032988	Persistent head lag	1	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0010862	Delayed fine motor development	1	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0002194	Delayed gross motor development	1	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0010862	Delayed fine motor development	1	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0032988	Persistent head lag	1	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0002194	Delayed gross motor development	1	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0010862	Delayed fine motor development	1	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0032988	Persistent head lag	1	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0002194	Delayed gross motor development	1	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0010862	Delayed fine motor development	1	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0032988	Persistent head lag	1	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0002194	Delayed gross motor development	1	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0032988	Persistent head lag	1	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0010862	Delayed fine motor development	1	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0032988	Persistent head lag	1	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0002194	Delayed gross motor development	1	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0032988	Persistent head lag	1	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0010862	Delayed fine motor development	1	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0002194	Delayed gross motor development	1	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0032988	Persistent head lag	1	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0010862	Delayed fine motor development	1	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0002194	Delayed gross motor development	1	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0010862	Delayed fine motor development	1	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0032988	Persistent head lag	1	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0002194	Delayed gross motor development	1	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0010862	Delayed fine motor development	1	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0032988	Persistent head lag	1	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0002194	Delayed gross motor development	1	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0010862	Delayed fine motor development	1	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0032988	Persistent head lag	1	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0002194	Delayed gross motor development	1	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0010862	Delayed fine motor development	1	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0032988	Persistent head lag	1	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0002194	Delayed gross motor development	1	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0010862	Delayed fine motor development	1	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0032988	Persistent head lag	1	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0032988	Persistent head lag	1	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0010862	Delayed fine motor development	1	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0002194	Delayed gross motor development	1	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0002194	Delayed gross motor development	1	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0010862	Delayed fine motor development	1	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0032988	Persistent head lag	1	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0010862	Delayed fine motor development	1	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0032988	Persistent head lag	1	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0002194	Delayed gross motor development	1	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0002194	Delayed gross motor development	1	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0010862	Delayed fine motor development	1	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0032988	Persistent head lag	1	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0002194	Delayed gross motor development	1	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0010862	Delayed fine motor development	1	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0032988	Persistent head lag	1	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0032988	Persistent head lag	1	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0010862	Delayed fine motor development	1	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0002194	Delayed gross motor development	1	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0002194	Delayed gross motor development	1	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0032988	Persistent head lag	1	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0010862	Delayed fine motor development	1	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0002194	Delayed gross motor development	1	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0010862	Delayed fine motor development	1	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0032988	Persistent head lag	1	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0002194	Delayed gross motor development	1	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0032988	Persistent head lag	1	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0010862	Delayed fine motor development	1	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0010862	Delayed fine motor development	1	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0032988	Persistent head lag	1	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0002194	Delayed gross motor development	1	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0032988	Persistent head lag	1	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0010862	Delayed fine motor development	1	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0002194	Delayed gross motor development	1	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0010862	Delayed fine motor development	1	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0032988	Persistent head lag	1	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0002194	Delayed gross motor development	1	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0010862	Delayed fine motor development	1	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0032988	Persistent head lag	1	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0002194	Delayed gross motor development	1	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0032988	Persistent head lag	1	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0032988	Persistent head lag	1	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0002194	Delayed gross motor development	1	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0010862	Delayed fine motor development	1	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0032988	Persistent head lag	1	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0002194	Delayed gross motor development	1	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0032988	Persistent head lag	1	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0010862	Delayed fine motor development	1	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0002194	Delayed gross motor development	1	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0032988	Persistent head lag	1	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0010862	Delayed fine motor development	1	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0002194	Delayed gross motor development	1	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0010862	Delayed fine motor development	1	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0032988	Persistent head lag	1	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0002194	Delayed gross motor development	1	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0032988	Persistent head lag	1	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0010862	Delayed fine motor development	1	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0002194	Delayed gross motor development	1	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0010862	Delayed fine motor development	1	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0032988	Persistent head lag	1	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0002194	Delayed gross motor development	1	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0010862	Delayed fine motor development	1	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0032988	Persistent head lag	1	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0010862	Delayed fine motor development	1	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0032988	Persistent head lag	1	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0002194	Delayed gross motor development	1	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0002194	Delayed gross motor development	1	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0032988	Persistent head lag	1	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0010862	Delayed fine motor development	1	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0002194	Delayed gross motor development	1	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0010862	Delayed fine motor development	1	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0032988	Persistent head lag	1	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0010862	Delayed fine motor development	1	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0032988	Persistent head lag	1	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0002194	Delayed gross motor development	1	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0025336	Delayed ability to sit	2	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0032989	Delayed ability to roll over	2	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0033128	Delayed ability to crawl	2	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0031936	Delayed ability to walk	2	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0025335	Delayed ability to stand	2	ADCY5 CL E G H	111	606703	Dyskinesia, familial, with facial myokymia	606703	C1847627	OMIM	0	653	236	600293
HP:0001270	HP:0032989	Delayed ability to roll over	2	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0033257	Delayed ability to walk with support	2	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0033128	Delayed ability to crawl	2	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0031936	Delayed ability to walk	2	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0025335	Delayed ability to stand	2	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0025336	Delayed ability to sit	2	AGRN CL E G H	375790	98914				ORPHA	0	2176	329	103320
HP:0001270	HP:0025335	Delayed ability to stand	2	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0025336	Delayed ability to sit	2	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0032989	Delayed ability to roll over	2	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0031936	Delayed ability to walk	2	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0033128	Delayed ability to crawl	2	ALG2 CL E G H	85365	616228	Myasthenic syndrome, congenital, 14	616228	C4015597	OMIM	0	335	23159	607905
HP:0001270	HP:0033128	Delayed ability to crawl	2	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0031936	Delayed ability to walk	2	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0025335	Delayed ability to stand	2	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0025336	Delayed ability to sit	2	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0032989	Delayed ability to roll over	2	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ANTXR1 CL E G H	84168	230740	Odontotrichomelic syndrome	230740	C0406723	OMIM	0	142	21014	606410
HP:0001270	HP:0025335	Delayed ability to stand	2	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0025336	Delayed ability to sit	2	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0032989	Delayed ability to roll over	2	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0033128	Delayed ability to crawl	2	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0031936	Delayed ability to walk	2	ATL1 CL E G H	51062	100984				ORPHA	0	517	11231	606439
HP:0001270	HP:0033128	Delayed ability to crawl	2	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0031936	Delayed ability to walk	2	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0025335	Delayed ability to stand	2	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0025336	Delayed ability to sit	2	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0032989	Delayed ability to roll over	2	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0033257	Delayed ability to walk with support	2	B3GAT3 CL E G H	26229	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	219	923	606374
HP:0001270	HP:0033128	Delayed ability to crawl	2	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0031936	Delayed ability to walk	2	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0025335	Delayed ability to stand	2	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0025336	Delayed ability to sit	2	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0032989	Delayed ability to roll over	2	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0033257	Delayed ability to walk with support	2	BICD2 CL E G H	23299	363454				ORPHA	0	740	17208	609797
HP:0001270	HP:0025335	Delayed ability to stand	2	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0025336	Delayed ability to sit	2	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0031936	Delayed ability to walk	2	CHAT CL E G H	1103	98914				ORPHA	0	984	1912	118490
HP:0001270	HP:0025336	Delayed ability to sit	2	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0032989	Delayed ability to roll over	2	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0033128	Delayed ability to crawl	2	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0031936	Delayed ability to walk	2	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0025335	Delayed ability to stand	2	CHST3 CL E G H	9469	245600	Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects	245600	C3278404	OMIM	0	445	1971	603799
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0031936	Delayed ability to walk	2	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0025335	Delayed ability to stand	2	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0025336	Delayed ability to sit	2	COL13A1 CL E G H	1305	98914				ORPHA	0	559	2190	120350
HP:0001270	HP:0032989	Delayed ability to roll over	2	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0033257	Delayed ability to walk with support	2	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0033128	Delayed ability to crawl	2	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0031936	Delayed ability to walk	2	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0025335	Delayed ability to stand	2	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0025336	Delayed ability to sit	2	COL13A1 CL E G H	1305	616720	Myasthenic syndrome, congenital, 19	616720	C4225235	OMIM	0	559	2190	120350
HP:0001270	HP:0025335	Delayed ability to stand	2	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0025336	Delayed ability to sit	2	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0032989	Delayed ability to roll over	2	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0033257	Delayed ability to walk with support	2	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0033128	Delayed ability to crawl	2	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0031936	Delayed ability to walk	2	CUL4B CL E G H	8450	300354	Syndromic X-linked mental retardation, Cabezas type	300354	C1845861	OMIM	0	415	2555	300304
HP:0001270	HP:0033128	Delayed ability to crawl	2	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0031936	Delayed ability to walk	2	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0025335	Delayed ability to stand	2	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0025336	Delayed ability to sit	2	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0032989	Delayed ability to roll over	2	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FIG4 CL E G H	9896	611228	Charcot-Marie-Tooth disease, type 4J	611228	C1970011	OMIM	0	926	16873	609390
HP:0001270	HP:0025336	Delayed ability to sit	2	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0032989	Delayed ability to roll over	2	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0033257	Delayed ability to walk with support	2	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0033128	Delayed ability to crawl	2	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0031936	Delayed ability to walk	2	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0025335	Delayed ability to stand	2	FKRP CL E G H	79147	34515				ORPHA	0	950	17997	606596
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0032989	Delayed ability to roll over	2	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0031936	Delayed ability to walk	2	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0033128	Delayed ability to crawl	2	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0025335	Delayed ability to stand	2	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0025336	Delayed ability to sit	2	GDAP1 CL E G H	54332	99944				ORPHA	0	537	15968	606598
HP:0001270	HP:0031936	Delayed ability to walk	2	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0033128	Delayed ability to crawl	2	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0025335	Delayed ability to stand	2	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0025336	Delayed ability to sit	2	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0032989	Delayed ability to roll over	2	GFPT1 CL E G H	2673	610542	Congenital myasthenic syndrome 12	610542	C3552335	OMIM	0	524	4241	138292
HP:0001270	HP:0025335	Delayed ability to stand	2	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0025336	Delayed ability to sit	2	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0032989	Delayed ability to roll over	2	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0033128	Delayed ability to crawl	2	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0031936	Delayed ability to walk	2	GMNN CL E G H	51053	616835	Meier-gorlin syndrome 6	616835	C4225188	OMIM	0	80	17493	602842
HP:0001270	HP:0031936	Delayed ability to walk	2	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0033128	Delayed ability to crawl	2	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0025335	Delayed ability to stand	2	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0025336	Delayed ability to sit	2	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0033257	Delayed ability to walk with support	2	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0032989	Delayed ability to roll over	2	GMPPB CL E G H	29925	615352	Muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14	615352	C3714932	OMIM	0	364	22932	615320
HP:0001270	HP:0033128	Delayed ability to crawl	2	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0031936	Delayed ability to walk	2	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0025335	Delayed ability to stand	2	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0025336	Delayed ability to sit	2	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0032989	Delayed ability to roll over	2	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HADH CL E G H	3033	71212				ORPHA	0	229	4799	601609
HP:0001270	HP:0033128	Delayed ability to crawl	2	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0031936	Delayed ability to walk	2	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0025335	Delayed ability to stand	2	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0025336	Delayed ability to sit	2	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0032989	Delayed ability to roll over	2	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HADHA CL E G H	3030	746	Apert like polydactyly syndrome			ORPHA	0	792	4801	600890
HP:0001270	HP:0025336	Delayed ability to sit	2	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0032989	Delayed ability to roll over	2	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0031936	Delayed ability to walk	2	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0033128	Delayed ability to crawl	2	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0025335	Delayed ability to stand	2	HADHB CL E G H	3032	746	Apert like polydactyly syndrome			ORPHA	0	367	4803	143450
HP:0001270	HP:0032989	Delayed ability to roll over	2	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0033128	Delayed ability to crawl	2	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0031936	Delayed ability to walk	2	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0025335	Delayed ability to stand	2	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0025336	Delayed ability to sit	2	HELLS CL E G H	3070	616911	Immunodeficiency-centromeric instability-facial anomalies syndrome 4	616911	C4310798	OMIM	0	297	4861	603946
HP:0001270	HP:0025335	Delayed ability to stand	2	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0025336	Delayed ability to sit	2	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0032989	Delayed ability to roll over	2	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0033128	Delayed ability to crawl	2	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0031936	Delayed ability to walk	2	HNMT CL E G H	3176	616739	Mental retardation, autosomal recessive 51	616739	C4225220	OMIM	0	53	5028	605238
HP:0001270	HP:0033128	Delayed ability to crawl	2	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0031936	Delayed ability to walk	2	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0025335	Delayed ability to stand	2	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0025336	Delayed ability to sit	2	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0032989	Delayed ability to roll over	2	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0033257	Delayed ability to walk with support	2	HSD17B4 CL E G H	3295	233400	Perrault syndrome 1	233400		OMIM	0	983	5213	601860
HP:0001270	HP:0033128	Delayed ability to crawl	2	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0031936	Delayed ability to walk	2	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0025335	Delayed ability to stand	2	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0025336	Delayed ability to sit	2	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0032989	Delayed ability to roll over	2	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	IGF1 CL E G H	3479	73272				ORPHA	0	197	5464	147440
HP:0001270	HP:0025335	Delayed ability to stand	2	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0025336	Delayed ability to sit	2	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0032989	Delayed ability to roll over	2	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0031936	Delayed ability to walk	2	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0033128	Delayed ability to crawl	2	KATNB1 CL E G H	10300	616212	Lissencephaly 6, with microcephaly	616212	C4015525	OMIM	0	314	6217	602703
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNA1 CL E G H	3736	37612				ORPHA	0	575	6218	176260
HP:0001270	HP:0033128	Delayed ability to crawl	2	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0031936	Delayed ability to walk	2	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0025335	Delayed ability to stand	2	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0025336	Delayed ability to sit	2	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0032989	Delayed ability to roll over	2	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KCNQ2 CL E G H	3785	121200	Benign familial neonatal seizures 1	121200	C1852587	OMIM	0	1962	6296	602235
HP:0001270	HP:0025335	Delayed ability to stand	2	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0025336	Delayed ability to sit	2	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0033257	Delayed ability to walk with support	2	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0032989	Delayed ability to roll over	2	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0031936	Delayed ability to walk	2	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0033128	Delayed ability to crawl	2	KMT2B CL E G H	9757	617284	Dystonia 28, childhood-onset	617284	C4310633	OMIM	0	1303	15840	606834
HP:0001270	HP:0032989	Delayed ability to roll over	2	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0033257	Delayed ability to walk with support	2	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0033128	Delayed ability to crawl	2	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0031936	Delayed ability to walk	2	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0025335	Delayed ability to stand	2	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0025336	Delayed ability to sit	2	LONP1 CL E G H	9361	600373	CODAS syndrome	600373	C1838180	OMIM	0	749	9479	605490
HP:0001270	HP:0025335	Delayed ability to stand	2	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0025336	Delayed ability to sit	2	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0032989	Delayed ability to roll over	2	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0033128	Delayed ability to crawl	2	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0031936	Delayed ability to walk	2	MAOA CL E G H	4128	300615	Monoamine oxidase A deficiency	300615	C0796275	OMIM	0	303	6833	309850
HP:0001270	HP:0032989	Delayed ability to roll over	2	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0033128	Delayed ability to crawl	2	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0031936	Delayed ability to walk	2	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0025335	Delayed ability to stand	2	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0025336	Delayed ability to sit	2	MECR CL E G H	51102	617282	Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities	617282	C4310634	OMIM	0	151	19691	608205
HP:0001270	HP:0032989	Delayed ability to roll over	2	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0033128	Delayed ability to crawl	2	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0031936	Delayed ability to walk	2	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0025335	Delayed ability to stand	2	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0025336	Delayed ability to sit	2	MORC2 CL E G H	22880	616688	Charcot-Marie-Tooth disease, axonal, type 2z	616688	C4225243	OMIM	0	726	23573	616661
HP:0001270	HP:0025335	Delayed ability to stand	2	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0025336	Delayed ability to sit	2	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0032989	Delayed ability to roll over	2	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0033128	Delayed ability to crawl	2	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0031936	Delayed ability to walk	2	MPZ CL E G H	4359	101082				ORPHA	0	607	7225	159440
HP:0001270	HP:0025336	Delayed ability to sit	2	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0031936	Delayed ability to walk	2	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0025335	Delayed ability to stand	2	MYH3 CL E G H	4621	193700	Freeman-Sheldon syndrome	193700	C0265224	OMIM	0	1136	7573	160720
HP:0001270	HP:0025335	Delayed ability to stand	2	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0025336	Delayed ability to sit	2	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0032989	Delayed ability to roll over	2	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0033257	Delayed ability to walk with support	2	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0033128	Delayed ability to crawl	2	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0031936	Delayed ability to walk	2	MYO9A CL E G H	4649	98914				ORPHA	0	280	7608	604875
HP:0001270	HP:0025336	Delayed ability to sit	2	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0031936	Delayed ability to walk	2	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0025335	Delayed ability to stand	2	NEFL CL E G H	4747	607684	Charcot-Marie-Tooth disease type 2E	607684	C1843225	OMIM	0	614	7739	162280
HP:0001270	HP:0033128	Delayed ability to crawl	2	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0031936	Delayed ability to walk	2	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0025335	Delayed ability to stand	2	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0025336	Delayed ability to sit	2	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0032989	Delayed ability to roll over	2	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NEK1 CL E G H	4750	263520	Short rib-polydactyly syndrome, Majewski type	263520	C0024507	OMIM	0	679	7744	604588
HP:0001270	HP:0025335	Delayed ability to stand	2	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0025336	Delayed ability to sit	2	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0032989	Delayed ability to roll over	2	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0033257	Delayed ability to walk with support	2	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0033128	Delayed ability to crawl	2	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0031936	Delayed ability to walk	2	NUS1 CL E G H	116150	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES	617831	CN757796	OMIM	0	326	21042	610463
HP:0001270	HP:0025336	Delayed ability to sit	2	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0032989	Delayed ability to roll over	2	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0033257	Delayed ability to walk with support	2	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0033128	Delayed ability to crawl	2	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0031936	Delayed ability to walk	2	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0025335	Delayed ability to stand	2	ORC6 CL E G H	23594	613803	Meier-Gorlin syndrome 3	613803	C3151113	OMIM	0	164	17151	607213
HP:0001270	HP:0031936	Delayed ability to walk	2	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0033128	Delayed ability to crawl	2	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0025335	Delayed ability to stand	2	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0025336	Delayed ability to sit	2	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0032989	Delayed ability to roll over	2	PAK1 CL E G H	5058	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY	618158		OMIM	0	79	8590	602590
HP:0001270	HP:0032989	Delayed ability to roll over	2	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0033128	Delayed ability to crawl	2	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0031936	Delayed ability to walk	2	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0025335	Delayed ability to stand	2	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0025336	Delayed ability to sit	2	PIEZO2 CL E G H	63895	617146	Arthrogryposis, distal, with impaired proprioception and touch	617146	C4310692	OMIM	0	978	26270	613629
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0031936	Delayed ability to walk	2	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0025335	Delayed ability to stand	2	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0025336	Delayed ability to sit	2	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMGNT1 CL E G H	55624	613157	Limb-girdle muscular dystrophy-dystroglycanopathy, type C3	613157	C3150417	OMIM	0	1174	19139	606822
HP:0001270	HP:0025336	Delayed ability to sit	2	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0032989	Delayed ability to roll over	2	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0033257	Delayed ability to walk with support	2	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0033128	Delayed ability to crawl	2	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0031936	Delayed ability to walk	2	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0025335	Delayed ability to stand	2	POMGNT2 CL E G H	84892	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8	618135	CN253928	OMIM	0	416	25902	614828
HP:0001270	HP:0025336	Delayed ability to sit	2	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0032989	Delayed ability to roll over	2	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0031936	Delayed ability to walk	2	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0033128	Delayed ability to crawl	2	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0025335	Delayed ability to stand	2	PRKRA CL E G H	8575	210571				ORPHA	0	192	9438	603424
HP:0001270	HP:0025336	Delayed ability to sit	2	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0032989	Delayed ability to roll over	2	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0033257	Delayed ability to walk with support	2	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0033128	Delayed ability to crawl	2	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0031936	Delayed ability to walk	2	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0025335	Delayed ability to stand	2	PTS CL E G H	5805	13	Brain malformation		C0266449	ORPHA	0	263	9689	612719
HP:0001270	HP:0025336	Delayed ability to sit	2	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0032989	Delayed ability to roll over	2	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0033128	Delayed ability to crawl	2	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0031936	Delayed ability to walk	2	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0025335	Delayed ability to stand	2	SH3PXD2B CL E G H	285590	249420	Frank Ter Haar syndrome	249420	C1855305	OMIM	0	524	29242	613293
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC18A3 CL E G H	6572	98914				ORPHA	0	305	10936	600336
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC25A1 CL E G H	6576	98914				ORPHA	0	568	10979	190315
HP:0001270	HP:0032989	Delayed ability to roll over	2	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0033128	Delayed ability to crawl	2	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0031936	Delayed ability to walk	2	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0025335	Delayed ability to stand	2	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0025336	Delayed ability to sit	2	SLC5A7 CL E G H	60482	98914				ORPHA	0	455	14025	608761
HP:0001270	HP:0025335	Delayed ability to stand	2	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0025336	Delayed ability to sit	2	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0032989	Delayed ability to roll over	2	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0031936	Delayed ability to walk	2	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0033128	Delayed ability to crawl	2	SNAP25 CL E G H	6616	98914				ORPHA	0	218	11132	600322
HP:0001270	HP:0033128	Delayed ability to crawl	2	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0031936	Delayed ability to walk	2	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0025335	Delayed ability to stand	2	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0025336	Delayed ability to sit	2	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0032989	Delayed ability to roll over	2	SPG21 CL E G H	51324	248900	Mast syndrome	248900	C1855346	OMIM	0	162	20373	608181
HP:0001270	HP:0032989	Delayed ability to roll over	2	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0033257	Delayed ability to walk with support	2	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0033128	Delayed ability to crawl	2	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0031936	Delayed ability to walk	2	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0025335	Delayed ability to stand	2	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0025336	Delayed ability to sit	2	SYT2 CL E G H	127833	98914				ORPHA	0	232	11510	600104
HP:0001270	HP:0031936	Delayed ability to walk	2	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0033128	Delayed ability to crawl	2	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0025335	Delayed ability to stand	2	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0025336	Delayed ability to sit	2	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0032989	Delayed ability to roll over	2	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TGFB3 CL E G H	7043	615582	Loeys-Dietz syndrome 5	615582	C3810012	OMIM	0	551	11769	190230
HP:0001270	HP:0033128	Delayed ability to crawl	2	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0031936	Delayed ability to walk	2	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0025335	Delayed ability to stand	2	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0025336	Delayed ability to sit	2	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0032989	Delayed ability to roll over	2	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TNFRSF11B CL E G H	4982	239000	Hyperphosphatasemia with bone disease	239000	C0268414	OMIM	0	208	11909	602643
HP:0001270	HP:0025335	Delayed ability to stand	2	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0025336	Delayed ability to sit	2	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0032989	Delayed ability to roll over	2	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0033257	Delayed ability to walk with support	2	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0033128	Delayed ability to crawl	2	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0031936	Delayed ability to walk	2	TSEN15 CL E G H	116461	617026	Pontocerebellar hypoplasia, type 2f	617026	C4310757	OMIM	0	65	16791	608756
HP:0001270	HP:0025336	Delayed ability to sit	2	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0032989	Delayed ability to roll over	2	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0033257	Delayed ability to walk with support	2	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0033128	Delayed ability to crawl	2	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0031936	Delayed ability to walk	2	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0025335	Delayed ability to stand	2	UBE3B CL E G H	89910	244450	Kaufman oculocerebrofacial syndrome	244450	C1855663	OMIM	0	316	13478	608047
HP:0001270	HP:0025335	Delayed ability to stand	2	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0025336	Delayed ability to sit	2	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0033257	Delayed ability to walk with support	2	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0032989	Delayed ability to roll over	2	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0031936	Delayed ability to walk	2	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0033128	Delayed ability to crawl	2	VAMP1 CL E G H	6843	98914				ORPHA	0	141	12642	185880
HP:0001270	HP:0032989	Delayed ability to roll over	2	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0033257	Delayed ability to walk with support	2	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0033128	Delayed ability to crawl	2	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0031936	Delayed ability to walk	2	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0025335	Delayed ability to stand	2	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0025336	Delayed ability to sit	2	VMA21 CL E G H	203547	310440	Myopathy, X-linked, with excessive autophagy	310440	C1839615	OMIM	0	254	22082	300913
HP:0001270	HP:0025336	Delayed ability to sit	2	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0032989	Delayed ability to roll over	2	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0033257	Delayed ability to walk with support	2	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0033128	Delayed ability to crawl	2	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0031936	Delayed ability to walk	2	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877
HP:0001270	HP:0025335	Delayed ability to stand	2	VPS13D CL E G H	55187	607317	Spinocerebellar ataxia autosomal recessive 4	607317	C1846492	OMIM	0	1034	23595	608877

Genes (424) :ABCC8 ACADSB ACTA1 ADA2 ADAMTS2 ADCY5 AGK AGRN AGTPBP1 AHCY AHI1 AK9 ALDH18A1 ALDH5A1 ALG14 ALG2 ALS2 AMPD2 ANTXR1 AP3B1 APOPT1 ARCN1 ARHGEF2 ARID2 ASAH1 ASPM ASXL3 ATG5 ATL1 ATP1A3 ATP2B3 ATP6AP2 ATP6V0A2 ATP6V1A ATP6V1E1 ATXN7 AUH B3GAT3 BCL11B BCOR BICD2 BIN1 BMP1 BRAT1 BRPF1 BSND CAMK2A CANT1 CDC6 CDK13 CFL2 CHAT CHD3 CHKB CHRNA1 CHRNB1 CHRND CHRNE CHST14 CHST3 CIB2 CLCNKA CLCNKB CLP1 CNTNAP2 COA7 COA8 COG1 COG4 COL11A2 COL12A1 COL13A1 COL1A1 COL1A2 COL2A1 COL6A1 COL6A2 COL6A3 COQ2 COQ7 COX10 COX14 COX20 COX6B1 COX8A CPLX1 CRAT CRPPA CTBP1 CTDP1 CUL4B CYP27B1 CYP2U1 DARS DARS2 DCX DHX30 DLAT DMD DMXL2 DNAJC19 DNM2 DOCK3 DOK7 DPAGT1 DPF2 DPYD DSE DYNC1H1 EBF3 EGR2 EIF2AK3 EP300 EPG5 ERLIN2 EXOSC2 EXTL3 FAM126A FASTKD2 FBN1 FBN2 FBXO11 FDX2 FGD4 FGF3 FGFR3 FIG4 FKBP14 FKRP FKTN FLNA FLRT1 FLVCR1 FOXG1 FOXP1 FRMPD4 FTSJ1 GALE GBA GCK GDAP1 GFM1 GFPT1 GHR GJB1 GJC2 GMNN GMPPB GRIA4 GRM1 GTF2E2 HACD1 HADH HADHA HADHB HARS HECW2 HELLS HEPACAM HERC2 HGSNAT HNMT HOXA1 HPRT1 HSD17B4 HUWE1 HYMAI IARS2 IFT52 IGF1 IGF1R IGF2 INPP5K INS IPW ISPD ITGA7 ITPR1 KAT6B KATNB1 KBTBD13 KCNA1 KCNA4 KCNC3 KCNJ11 KCNQ2 KDM1A KDM5B KIDINS220 KIF14 KIF7 KLC2 KLHL40 KLHL41 KMT2A KMT2B KY LAMA1 LAMA2 LARGE1 LARS LIAS LMNA LMOD3 LONP1 LRP4 LRP5 LTBP4 MAGEL2 MAOA MAP3K20 MAPRE2 MBD5 MBOAT7 MCM3AP MECR MED12 MED13L MEF2C MEGF10 MFN2 MICU1 MKRN3 MKRN3-AS1 MLC1 MMP13 MORC2 MPDZ MPZ MSTO1 MT-TN MT-TS1 MT-TW MTMR14 MTMR2 MTPAP MUSK MYF6 MYH3 MYH7 MYL2 MYMK MYO7A MYO9A MYPN NAA10 NAA15 NDN NDUFA1 NDUFA12 NEB NEFL NEK1 NFIX NKX2-1 NKX6-2 NONO NOTCH3 NPAP1 NPHP1 NRAS NT5C2 NUS1 OPA1 ORC6 PACS2 PAK1 PAK3 PBX1 PCBD1 PCDH15 PDE10A PDX1 PET100 PHKA2 PHKG2 PIEZO2 PIGC PLAGL1 PLEC PLOD1 PLXND1 PMP22 PNKP PNP PNPLA2 POMGNT1 POMGNT2 POMK POMT1 POMT2 PPP2R1A PREPL PRKRA PRMT7 PRPS1 PRX PTCH1 PTCH2 PTEN PTPRQ PTS PUM1 PWAR1 PWRN1 RAB11B RAPSN RBM8A REPS1 REV3L RNU12 RORA RPS23 RPS6KA3 RSPRY1 RUBCN RUSC2 RYR1 SAMD9 SCN11A SCN1A SCN4A SCO1 SCO2 SCYL1 SDHA SDHAF1 SDHB SDHD SELENON SET SETBP1 SH3PXD2B SH3TC2 SHANK3 SLC12A6 SLC18A2 SLC18A3 SLC1A3 SLC25A1 SLC5A7 SLC6A3 SLC6A8 SLC9A1 SMARCAL1 SMC1A SNAP25 SNORD115-1 SNORD116-1 SNRPN SOX5 SP7 SPARC SPART SPEG SPG21 SPR SRD5A3 STAC3 STAT3 SUCLA2 SUFU SYNGAP1 SYT1 SYT2 TACO1 TAF1 TAZ TBC1D24 TCF4 TENT5A TGFB3 TH TIMM50 TK2 TLK2 TMCO1 TMEM94 TMTC3 TNFRSF11A TNFRSF11B TNNT1 TNPO3 TPM2 TPM3 TRAPPC9 TRIO TRIP11 TRIP4 TRMT1 TRMT10A TRMU TRNE TRNN TRNS1 TRNW TRPV4 TRPV6 TSEN15 TSHR TTN TUBA1A TUBB TUBB2B TUBB3 TUBB4A UBE3A UBE3B USH1C VAMP1 VDR VMA21 VPS13B VPS13D WDR26 WDR73 WWOX ZBTB24 ZEB2 ZFP57 ZNF148 ZNF592 ZNF711 ZSWIM6

Diseases (425) :99885 99886 606176 610006 171433 2020 171439 171430 161800 820 225410 606703 212350 98914 618276 613752 447760 271980 353327 616228 607225 230740 608233 617164 617523 617808 228000 608716 100984 182600 71517 314978 302500 300423 357074 219200 617403 94147 250950 245600 309800 300166 363454 618291 615290 169186 255200 602522 251450 613805 602541 608930 608931 601776 263463 614869 613090 220110 436271 618150 616470 616720 156550 158810 254090 607426 616733 617917 370980 617915 604168 300354 264700 615030 615281 611105 300067 98896 616113 160150 614750 274270 614228 605253 145900 1667 242840 617763 617425 610532 284979 121050 251900 609311 100800 611228 300179 614557 34515 613153 613152 611588 309350 613454 231000 99944 214400 609060 610542 633 1175 302800 608804 616835 615352 617691 616943 71212 746 616911 604004 613925 613926 176270 252930 616739 300322 233400 436174 616007 617102 73272 608747 73273 270450 616489 617404 613204 206700 117360 603736 616212 37612 618284 98768 605259 121200 616728 607131 609541 615731 617284 615960 607855 618138 258 608840 614462 613205 600373 300615 617760 616734 156200 618124 617282 305450 616789 613443 614399 615673 250400 616688 615219 101082 180800 502423 617675 601382 254343 193700 254940 276900 171881 617787 256030 607684 607734 617882 263520 602535 614753 118700 610978 617560 300967 130720 613224 320396 613162 617831 210000 613803 618158 617641 264070 602083 494526 616921 306000 613027 617146 613723 225400 570 613402 613179 98908 613151 613157 618135 616094 609308 613156 613158 616224 210571 612067 311070 300661 614895 109400 613391 13 617931 274000 618060 617412 300844 616723 615705 98905 597 324581 424107 117000 255320 617053 615548 607208 614198 521411 616719 3208 602771 616078 249420 601596 606232 218000 612656 300352 616291 242900 313892 613849 616507 101000 275900 615959 248900 70594 612379 612713 255995 612621 302060 610954 617952 615582 101150 605407 254875 618050 213980 612301 239000 98902 609285 609284 617061 184260 486815 617066 616033 181405 618188 617026 424 99819 609152 611705 611603 156610 610031 612438 105830 244450 277440 310440 216550 607317 83472 284282 614069 235730 300803 324588 98913 401805 169189 614856 610687 143095 411493 610042 3450 130060 617821 352582 245348 66634 615539 613684 209951 610706 606612 320406 88628 613670 309549 230350 320401 614504 601536 85328 208513 521390 617914 319182 496689 615438 2788 617087 324604 276432 609583 300558 254361 616362 109 512260 404499 178145 613135 1933 612073 300966 609560 605355 254864 300570 608629 615686 615485 617584 618012 618092 618056 617333 617798 617360 618205 611209 616471 617976 617804 618292 618027 158600 617330 611225 618089 609033 300983 617864 617268 618109 615547 617188 618184 613672 618198 301020 618244 618067 617816 617157 617807 617916 617773 618106 618049 618197 617143 618218 617698 618316 617255 608423 613192 618302 617616 617260 617865

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.

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