Human Phenotype Ontology

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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:
Abnormal cerebellum morphology (HP:0001317)

Grandparent Node:
Aplasia/Hypoplasia involving the central nervous system (HP:0002977)

Parent Node:
Aplasia/Hypoplasia of the cerebellum (HP:0007360)

..Starting node
..Cerebellar hypoplasia (HP:0001321)

Term ID:

1321

Name:

Cerebellar hypoplasia

Synonym:

Congenital cerebellar hypoplasia; Hypoplasia of cerebellum; Hypoplastic cerebellum; Small cerebellum; Underdeveloped cerebellum

Definition:

Cerebellar hypoplasia is a descriptive term implying a cerebellum with a reduced volume, but a normal shape and is stable over time.

Comments:

Reference:

HP:0001321

Genes and Diseases:

Child Nodes:

........

Olivopontocerebellar hypoplasia (HP:0006955)

........

Cerebellar hemisphere hypoplasia (HP:0100307)

Sister Nodes:

Cerebellar agenesis (HP:0012642)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ABAT CL E G H	18	23	OMIM:613163	GABA-transaminase deficiency	.	120
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ACD CL E G H	65057	25070	OMIM:616553	Dyskeratosis congenita, autosomal dominant 6	.	11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ACD CL E G H	65057	25070	ORPHA:3322	Hoyeraal-Hreidarsson syndrome	HP:0040281 - Very frequent	11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ADGRG1 CL E G H	9289	4512	ORPHA:101070	Bilateral frontoparietal polymicrogyria		88
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ADGRG1 CL E G H	9289	4512	ORPHA:98889	Bilateral perisylvian polymicrogyria		88
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ADGRG1 CL E G H	9289	4512	OMIM:606854	Polymicrogyria, bilateral frontoparietal	.	88
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AFF3 CL E G H	3899	6473	OMIM:619297	KINSSHIP SYNDROME; KINS		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AFG3L2 CL E G H	10939	315	ORPHA:313772	Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome	HP:0040282 - Frequent	86
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AHCY CL E G H	191	343	ORPHA:88618	S-adenosylhomocysteine hydrolase deficiency	HP:0040282 - Frequent	31
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AHI1 CL E G H	54806	21575	ORPHA:475	Joubert syndrome		175
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AHI1 CL E G H	54806	21575	OMIM:608629	Joubert syndrome 3		175
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AHI1 CL E G H	54806	21575	ORPHA:220493	Joubert syndrome with ocular defect		175
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ALG12 CL E G H	79087	19358	ORPHA:79324	ALG12-CDG	HP:0040283 - Occasional	68
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ALG3 CL E G H	10195	23056	ORPHA:79321	ALG3-CDG		37
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ALG6 CL E G H	29929	23157	ORPHA:79320	ALG6-CDG	HP:0040284 - Very rare	66
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ALX4 CL E G H	60529	450	OMIM:613451	Frontonasal dysplasia 2		132
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	AP1S2 CL E G H	8905	560	OMIM:304340	Pettigrew syndrome		13
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	APC2 CL E G H	10297	24036	OMIM:618677	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 10; CDCBM10		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	APC2 CL E G H	10297	24036	ORPHA:821	Sotos syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARHGEF2 CL E G H	9181	682	OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARID1A CL E G H	8289	11110	ORPHA:1465	Coffin-Siris syndrome		88
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARID1A CL E G H	8289	11110	OMIM:614607	Coffin-Siris syndrome 2		88
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARID1B CL E G H	57492	18040	ORPHA:1465	Coffin-Siris syndrome		219
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARID1B CL E G H	57492	18040	OMIM:135900	Coffin-Siris syndrome 1		219
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARID2 CL E G H	196528	18037	ORPHA:1465	Coffin-Siris syndrome		25
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARL13B CL E G H	200894	25419	ORPHA:475	Joubert syndrome		62
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARL3 CL E G H	403	694	ORPHA:475	Joubert syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARL3 CL E G H	403	694	OMIM:618161	JOUBERT SYNDROME 35; JBTS35		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARMC9 CL E G H	80210	20730	ORPHA:475	Joubert syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARMC9 CL E G H	80210	20730	OMIM:617622	JOUBERT SYNDROME 30; JBTS30
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ARSI CL E G H	340075	32521	ORPHA:401815	Autosomal recessive spastic paraplegia type 66	HP:0040282 - Frequent	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ASNS CL E G H	440	753	OMIM:615574	Asparagine synthetase deficiency	.	17
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ASPM CL E G H	259266	19048	OMIM:608716	Microcephaly 5, primary, autosomal recessive	HP:0040283 - Occasional	512
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ASXL1 CL E G H	171023	18318	ORPHA:97297	Bohring-Opitz syndrome		145
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ASXL1 CL E G H	171023	18318	OMIM:605039	Bohring-Opitz syndrome		145
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ASXL3 CL E G H	80816	29357	ORPHA:352577	Bainbridge-Ropers syndrome		49
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ASXL3 CL E G H	80816	29357	OMIM:615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		49
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATAD3A CL E G H	55210	25567	OMIM:618810	PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL; PHRINL		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATCAY CL E G H	85300	779	OMIM:601238	Cerebellar ataxia, Cayman type		72
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATCAY CL E G H	85300	779	ORPHA:94122	Cerebellar ataxia, Cayman type	HP:0040282 - Frequent	72
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATG5 CL E G H	9474	589	OMIM:617584	Spinocerebellar ataxia, autosomal recessive 25	.	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATG7 CL E G H	10533	16935	OMIM:619422	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 31; SCAR31		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATN1 CL E G H	1822	3033	OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies		16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP2B3 CL E G H	492	816	ORPHA:314978	X-linked non progressive cerebellar ataxia	HP:0040282 - Frequent	19
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP5F1A CL E G H	498	823	OMIM:615228	Mitochondrial complex V (atp synthase) deficiency, nuclear type 4	.
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V0A1 CL E G H	535	865	OMIM:619971			1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V0A2 CL E G H	23545	18481	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	HP:0040282 - Frequent	140
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V0A2 CL E G H	23545	18481	OMIM:219200	Cutis laxa, autosomal recessive, type IIA		140
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V0A2 CL E G H	23545	18481	ORPHA:2834	Wrinkly skin syndrome		140
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V1A CL E G H	523	851	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	HP:0040282 - Frequent	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V1B2 CL E G H	526	854	ORPHA:79500	DOORS syndrome		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATP6V1E1 CL E G H	529	857	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	HP:0040282 - Frequent	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATR CL E G H	545	882	OMIM:210600	Seckel syndrome 1		168
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ATXN2 CL E G H	6311	10555	ORPHA:98756	Spinocerebellar ataxia type 2		11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B3GALNT2 CL E G H	148789	28596	OMIM:615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11	.	43
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B3GALNT2 CL E G H	148789	28596	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	43
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B4GALT1 CL E G H	2683	924	ORPHA:79332	B4GALT1-CDG		85
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B4GALT1 CL E G H	2683	924	OMIM:607091	Congenital disorder of glycosylation, type IID		85
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B4GAT1 CL E G H	11041	15685	OMIM:615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13	.	17
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B4GAT1 CL E G H	11041	15685	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	17
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B9D1 CL E G H	27077	24123	ORPHA:475	Joubert syndrome		28
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B9D1 CL E G H	27077	24123	ORPHA:564	Meckel syndrome		28
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B9D2 CL E G H	80776	28636	ORPHA:475	Joubert syndrome		34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B9D2 CL E G H	80776	28636	ORPHA:564	Meckel syndrome		34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	B9D2 CL E G H	80776	28636	OMIM:614175	Meckel syndrome, type 10		34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BCOR CL E G H	54880	20893	OMIM:300166	Microphthalmia, syndromic 2		101
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BICD2 CL E G H	23299	17208	OMIM:618291	Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant	.	46
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BLTP1 CL E G H	84162	26953	OMIM:617822	Alkuraya-Kucinskas syndrome	.
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BMP4 CL E G H	652	1071	ORPHA:139471	Microphthalmia with brain and digit anomalies		38
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BMP4 CL E G H	652	1071	OMIM:607932	Microphthalmia, syndromic 6		38
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BRF1 CL E G H	2972	11551	ORPHA:444072	Cerebellar-facial-dental syndrome	HP:0040281 - Very frequent	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BRF1 CL E G H	2972	11551	OMIM:616202	Cerebellofaciodental syndrome	.	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BUB1 CL E G H	699	1148	ORPHA:1052	Mosaic variegated aneuploidy syndrome		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BUB1B CL E G H	701	1149	ORPHA:1052	Mosaic variegated aneuploidy syndrome		76
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BUB1B CL E G H	701	1149	OMIM:257300	Mosaic variegated aneuploidy syndrome 1	.	76
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	BUB3 CL E G H	9184	1151	ORPHA:1052	Mosaic variegated aneuploidy syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	C2CD3 CL E G H	26005	24564	ORPHA:434179	Orofaciodigital syndrome type 14		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	C2CD3 CL E G H	26005	24564	OMIM:615948	Orofaciodigital syndrome XIV	.	27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CACNA1G CL E G H	8913	1394	OMIM:618087	Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits	.	32
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CAMTA1 CL E G H	23261	18806	OMIM:614756	Cerebellar ataxia, nonprogressive, with mental retardation	HP:0040283 - Occasional	34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CAMTA1 CL E G H	23261	18806	ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability	HP:0040282 - Frequent	34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CARS2 CL E G H	79587	25695	OMIM:616672	Combined oxidative phosphorylation deficiency 27	.	35
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CASK CL E G H	8573	1497	OMIM:300749	Mental retardation and microcephaly with pontine and cerebellar hypoplasia		118
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CASK CL E G H	8573	1497	ORPHA:163937	X-linked intellectual disability, Najm type	HP:0040281 - Very frequent	118
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CBY1 CL E G H	25776	1307	ORPHA:475	Joubert syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CC2D2A CL E G H	57545	29253	OMIM:619111	COACH SYNDROME 2; COACH2		247
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CC2D2A CL E G H	57545	29253	ORPHA:1454	Joubert syndrome with hepatic defect		247
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CC2D2A CL E G H	57545	29253	ORPHA:2318	Joubert syndrome with oculorenal defect		247
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CC2D2A CL E G H	57545	29253	ORPHA:564	Meckel syndrome		247
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CCDC22 CL E G H	28952	28909	ORPHA:7	3C syndrome		33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CCDC22 CL E G H	28952	28909	OMIM:300963	Ritscher-Schinzel syndrome 2	.	33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CCDC32 CL E G H	90416	28295	OMIM:619123	CARDIOFACIONEURODEVELOPMENTAL SYNDROME; CFNDS		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CDC40 CL E G H	51362	17350	OMIM:619302	PONTOCEREBELLAR HYPOPLASIA, TYPE 15; PCH15
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CDC42 CL E G H	998	1736	ORPHA:487796	Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome		6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CDC42 CL E G H	998	1736	OMIM:616737	Takenouchi-Kosaki syndrome	.	6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CDC42BPB CL E G H	9578	1738	OMIM:619841
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CDK5 CL E G H	1020	1774	OMIM:616342	Lissencephaly 7 with cerebellar hypoplasia	.	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CDKN1C CL E G H	1028	1786	OMIM:130650	Beckwith-Wiedemann syndrome		114
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CENPE CL E G H	1062	1856	OMIM:616051	Microcephaly 13, primary, autosomal recessive	.	20
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CENPF CL E G H	1063	1857	OMIM:243605	Stromme syndrome	.	27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP104 CL E G H	9731	24866	ORPHA:475	Joubert syndrome		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP104 CL E G H	9731	24866	OMIM:616781	Joubert syndrome 25	.	5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP120 CL E G H	153241	26690	ORPHA:475	Joubert syndrome		7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP120 CL E G H	153241	26690	ORPHA:220493	Joubert syndrome with ocular defect		7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP120 CL E G H	153241	26690	OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly	.	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP164 CL E G H	22897	29182	OMIM:614845	Nephronophthisis 15		34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP290 CL E G H	80184	29021	ORPHA:2318	Joubert syndrome with oculorenal defect		342
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP290 CL E G H	80184	29021	ORPHA:564	Meckel syndrome		342
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP290 CL E G H	80184	29021	OMIM:611134	Meckel syndrome, type 4		342
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP41 CL E G H	95681	12370	ORPHA:475	Joubert syndrome		90
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP41 CL E G H	95681	12370	ORPHA:220493	Joubert syndrome with ocular defect		90
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP55 CL E G H	55165	1161	OMIM:236500	Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CEP57 CL E G H	9702	30794	ORPHA:1052	Mosaic variegated aneuploidy syndrome		17
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CHD7 CL E G H	55636	20626	ORPHA:138	CHARGE syndrome		515
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CHMP1A CL E G H	5119	8740	OMIM:614961	Pontocerebellar hypoplasia, type 8	.	19
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CIT CL E G H	11113	1985	OMIM:617090	Microcephaly 17, primary, autosomal recessive	.	15
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CLCN3 CL E G H	1182	2021	OMIM:619512	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES; NEDHYBA		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	COASY CL E G H	80347	29932	OMIM:618266	Pontocerebellar hypoplasia, type 12	.	16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	COG1 CL E G H	9382	6545	ORPHA:263508	COG1-CDG		52
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	COL3A1 CL E G H	1281	2201	OMIM:618343	Polymicrogyria with or without vascular-type ehlers-danlos syndrome	.	749
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	COL4A1 CL E G H	1282	2202	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	193
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	COQ4 CL E G H	51117	19693	OMIM:616276	Coenzyme Q10 deficiency, primary, 7	HP:0040283 - Occasional	24
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CPLANE1 CL E G H	65250	25801	ORPHA:475	Joubert syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CPLANE1 CL E G H	65250	25801	ORPHA:2754	Orofaciodigital syndrome type 6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CPLANE1 CL E G H	65250	25801	OMIM:277170	Orofaciodigital syndrome VI
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CPSF3 CL E G H	51692	2326	OMIM:619876
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CPT2 CL E G H	1376	2330	ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form		101
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CPT2 CL E G H	1376	2330	ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		101
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CRPPA CL E G H	729920	37276	OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7	.
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CRPPA CL E G H	729920	37276	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CSF1R CL E G H	1436	2433	OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis	.	149
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CSPP1 CL E G H	79848	26193	ORPHA:475	Joubert syndrome		57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CSPP1 CL E G H	79848	26193	ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	HP:0040282 - Frequent	57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CSPP1 CL E G H	79848	26193	ORPHA:564	Meckel syndrome		57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CTNNA2 CL E G H	1496	2510	OMIM:618174	Cortical dysplasia, complex, with other brain malformations 9	.	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CWF19L1 CL E G H	55280	25613	ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency		9
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	CWF19L1 CL E G H	55280	25613	OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17	.	9
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DAG1 CL E G H	1605	2666	ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy		108
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DAG1 CL E G H	1605	2666	OMIM:616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9		108
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DAG1 CL E G H	1605	2666	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	108
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DCHS1 CL E G H	8642	13681	ORPHA:314679	Cerebrofacioarticular syndrome		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DENND5A CL E G H	23258	19344	OMIM:617281	Epileptic encephalopathy, early infantile, 49		6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DHCR7 CL E G H	1717	2860	OMIM:270400	Smith-Lemli-Opitz syndrome		159
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DHFR CL E G H	1719	2861	OMIM:613839	Megaloblastic anemia due to dihydrofolate reductase deficiency	.	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DHX37 CL E G H	57647	17210	OMIM:618731	NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES; NEDBAVC		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DISC1 CL E G H	27185	2888	ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome	HP:0040282 - Frequent	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DKC1 CL E G H	1736	2890	OMIM:305000	Dyskeratosis congenita, X-linked	HP:0040283 - Occasional	65
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DKC1 CL E G H	1736	2890	ORPHA:3322	Hoyeraal-Hreidarsson syndrome	HP:0040281 - Very frequent	65
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DMXL2 CL E G H	23312	2938	OMIM:616113	Polyendocrine-Polyneuropathy syndrome	HP:0040283 - Occasional	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DMXL2 CL E G H	23312	2938	ORPHA:453533	Polyendocrine-polyneuropathy syndrome	HP:0040283 - Occasional	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DOCK6 CL E G H	57572	19189	OMIM:614219	Adams-Oliver syndrome 2	HP:0040283 - Occasional	18
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DOK7 CL E G H	285489	26594	ORPHA:994	Fetal akinesia deformation sequence		91
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPAGT1 CL E G H	1798	2995	ORPHA:86309	DPAGT1-CDG	HP:0040283 - Occasional	38
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPF2 CL E G H	5977	9964	ORPHA:1465	Coffin-Siris syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPH1 CL E G H	1801	3003	ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPH1 CL E G H	1801	3003	OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPH5 CL E G H	51611	24270	OMIM:620070
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPM2 CL E G H	8818	3006	OMIM:615042	Congenital disorder of glycosylation, type Iu	.	26
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPM2 CL E G H	8818	3006	ORPHA:329178	Congenital muscular dystrophy with intellectual disability and severe epilepsy	HP:0040282 - Frequent	26
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DPYSL5 CL E G H	56896	20637	OMIM:619435	RITSCHER-SCHINZEL SYNDROME 4; RTSC4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DYNC1H1 CL E G H	1778	2961	OMIM:614563	Mental retardation, autosomal dominant 13	HP:0040283 - Occasional	427
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DYNC2H1 CL E G H	79659	2962	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional	304
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DYNC2I1 CL E G H	55112	21862	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	DYNC2I2 CL E G H	89891	28296	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EBF3 CL E G H	253738	19087	OMIM:617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		25
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EBP CL E G H	10682	3133	OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		51
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EBP CL E G H	10682	3133	ORPHA:401973	MEND syndrome		51
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EBP CL E G H	10682	3133	OMIM:300960	Mend syndrome		51
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EHMT1 CL E G H	79813	24650	ORPHA:261652	Kleefstra syndrome due to a point mutation	HP:0040283 - Occasional	223
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ELN CL E G H	2006	3327	OMIM:194050	Williams-Beuren syndrome		172
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EOMES CL E G H	8320	3372	ORPHA:171703	Microcephaly-polymicrogyria-corpus callosum agenesis syndrome	HP:0040282 - Frequent	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EPG5 CL E G H	57724	29331	OMIM:242840	Vici syndrome		40
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EPG5 CL E G H	57724	29331	ORPHA:1493	Vici syndrome	HP:0040282 - Frequent	40
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ERCC1 CL E G H	2067	3433	OMIM:610758	Cerebrooculofacioskeletal syndrome 4	.	20
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ERCC5 CL E G H	2073	3437	OMIM:616570	Cerebrooculofacioskeletal syndrome 3		83
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ERCC6 CL E G H	2074	3438	OMIM:214150	Cerebrooculofacioskeletal syndrome 1	.	199
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ERF CL E G H	2077	3444	ORPHA:207	Crouzon disease	HP:0040282 - Frequent	12
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ERMARD CL E G H	55780	21056	ORPHA:75857	6q terminal deletion syndrome	HP:0040281 - Very frequent	36
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ESCO2 CL E G H	157570	27230	ORPHA:2319	Juberg-Hayward syndrome		92
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EVC CL E G H	2121	3497	OMIM:225500	Ellis-Van creveld syndrome		209
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EVC2 CL E G H	132884	19747	OMIM:225500	Ellis-Van creveld syndrome		137
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EXOC2 CL E G H	55770	24968	OMIM:619306	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA; NEDFACH		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EXOC7 CL E G H	23265	23214	OMIM:619072	NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY; NEDSEBA
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EXOSC1 CL E G H	51013	17286	OMIM:619304	PONTOCEREBELLAR HYPOPLASIA, TYPE 1F; PCH1F
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EXOSC8 CL E G H	11340	17035	OMIM:616081	Pontocerebellar hypoplasia, type 1C		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	EZH2 CL E G H	2146	3527	OMIM:277590	Weaver syndrome		81
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FAM149B1 CL E G H	317662	29162	ORPHA:2754	Orofaciodigital syndrome type 6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FANCB CL E G H	2187	3583	OMIM:300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		58
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FANCL CL E G H	55120	20748	OMIM:614083	Fanconi anemia, complementation group L		53
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FAR1 CL E G H	84188	26222	ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FAR1 CL E G H	84188	26222	OMIM:616154	PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER; PFCRD		7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FAT4 CL E G H	79633	23109	ORPHA:314679	Cerebrofacioarticular syndrome		114
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FDXR CL E G H	2232	3642	ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FGFR1 CL E G H	2260	3688	OMIM:613001	Encephalocraniocutaneous lipomatosis	.	172
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FGFR2 CL E G H	2263	3689	OMIM:101200	Apert syndrome		175
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FGFR2 CL E G H	2263	3689	ORPHA:207	Crouzon disease	HP:0040282 - Frequent	175
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FIG4 CL E G H	9896	16873	ORPHA:3472	Yunis-Varon syndrome	HP:0040283 - Occasional	111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FIG4 CL E G H	9896	16873	OMIM:216340	Yunis-Varon syndrome	HP:0040283 - Occasional	111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKRP CL E G H	79147	17997	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040282 - Frequent	157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKRP CL E G H	79147	17997	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKRP CL E G H	79147	17997	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKRP CL E G H	79147	17997	OMIM:613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5	.	157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKRP CL E G H	79147	17997	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKTN CL E G H	2218	3622	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		184
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKTN CL E G H	2218	3622	OMIM:253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4	.	184
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FKTN CL E G H	2218	3622	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	184
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FLNA CL E G H	2316	3754	OMIM:300049	Heterotopia, periventricular, X-linked dominant		493
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FLNA CL E G H	2316	3754	ORPHA:90652	Otopalatodigital syndrome type 2	HP:0040282 - Frequent	493
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FLVCR2 CL E G H	55640	20105	OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome	.	47
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FOXC1 CL E G H	2296	3800	OMIM:601631	Anterior segment dysgenesis 3		63
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FOXC1 CL E G H	2296	3800	OMIM:602482	Axenfeld-rieger syndrome, type 3		63
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FRMD4A CL E G H	55691	25491	OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia	.	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FRMD4A CL E G H	55691	25491	ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	FTO CL E G H	79068	24678	OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		70
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GEMIN4 CL E G H	50628	15717	OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GFM2 CL E G H	84340	29682	ORPHA:565624	Combined oxidative phosphorylation defect type 39	HP:0040282 - Frequent	43
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GJB2 CL E G H	2706	4284	ORPHA:477	KID syndrome	HP:0040283 - Occasional	199
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GJB6 CL E G H	10804	4288	ORPHA:477	KID syndrome	HP:0040283 - Occasional	56
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GLI3 CL E G H	2737	4319	ORPHA:36	Acrocallosal syndrome		270
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GLI3 CL E G H	2737	4319	ORPHA:672	Pallister-Hall syndrome	HP:0040283 - Occasional	270
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GMPPB CL E G H	29925	22932	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040282 - Frequent	34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GMPPB CL E G H	29925	22932	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GMPPB CL E G H	29925	22932	OMIM:615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14	.	34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GMPPB CL E G H	29925	22932	OMIM:615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14	HP:0040283 - Occasional	34
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GOT2 CL E G H	2806	4433	OMIM:618721	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 82; DEE82
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPAA1 CL E G H	8733	4446	OMIM:617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPAA1 CL E G H	8733	4446	ORPHA:529665	Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome	HP:0040282 - Frequent
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPC3 CL E G H	2719	4451	ORPHA:373	Simpson-Golabi-Behmel syndrome		73
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPC3 CL E G H	2719	4451	OMIM:312870	Simpson-golabi-behmel syndrome, type 1		73
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPC4 CL E G H	2239	4452	ORPHA:373	Simpson-Golabi-Behmel syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPC4 CL E G H	2239	4452	OMIM:312870	Simpson-golabi-behmel syndrome, type 1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPHN CL E G H	10243	15465	OMIM:615501	Molybdenum cofactor deficiency, complementation group C	.	18
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPSM2 CL E G H	29899	29501	OMIM:604213	CHUDLEY-MCCULLOUGH SYNDROME; CMCS		74
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GPX4 CL E G H	2879	4556	ORPHA:93317	Spondylometaphyseal dysplasia, Sedaghatian type	HP:0040282 - Frequent	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GRIA3 CL E G H	2892	4573	ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations		30
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GRM1 CL E G H	2911	4593	OMIM:614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13; SCAR13		8
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	GTPBP2 CL E G H	54676	4670	OMIM:617988	Jaberi-Elahi syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	H19-ICR CL E G H	105259599		OMIM:130650	Beckwith-Wiedemann syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	H3-3A CL E G H	3020	4764	OMIM:619720	BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 1; BRYLIB1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HDAC6 CL E G H	10013	14064	ORPHA:163966	X-linked dominant chondrodysplasia, Chassaing-Lacombe type	HP:0040283 - Occasional	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HERC1 CL E G H	8925	4867	ORPHA:457359	Megalencephaly-severe kyphoscoliosis-overgrowth syndrome	HP:0040283 - Occasional	16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HHAT CL E G H	55733	18270	OMIM:600092	Nivelon-Nivelon-Mabille syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HNRNPH1 CL E G H	3187	5041	OMIM:620083
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HNRNPH2 CL E G H	3188	5042	OMIM:300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HNRNPR CL E G H	10236	5047	OMIM:620073
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HRAS CL E G H	3265	5173	ORPHA:2612	Linear nevus sebaceus syndrome		113
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HYLS1 CL E G H	219844	26558	OMIM:236680	Hydrolethalus syndrome 1		31
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	HYLS1 CL E G H	219844	26558	ORPHA:475	Joubert syndrome		31
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	IER3IP1 CL E G H	51124	18550	OMIM:614231	Microcephaly, epilepsy, and diabetes syndrome	HP:0040283 - Occasional	6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	IFT172 CL E G H	26160	30391	OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly		48
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	IFT80 CL E G H	57560	29262	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional	65
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	IGF2 CL E G H	3481	5466	OMIM:130650	Beckwith-Wiedemann syndrome		9
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INPP5E CL E G H	56623	21474	ORPHA:475	Joubert syndrome		111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INPP5E CL E G H	56623	21474	OMIM:213300	Joubert syndrome 1		111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INPP5E CL E G H	56623	21474	ORPHA:1454	Joubert syndrome with hepatic defect		111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INPP5E CL E G H	56623	21474	ORPHA:220493	Joubert syndrome with ocular defect		111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INPP5K CL E G H	51763	33882	ORPHA:559	Marinesco-Sjögren syndrome	HP:0040281 - Very frequent	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INTS1 CL E G H	26173	24555	OMIM:618571	NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES; NDCAGF
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	INTS8 CL E G H	55656	26048	OMIM:618572	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY; NEDCHS		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ITPR1 CL E G H	3708	6180	OMIM:206700	Gillespie syndrome	.	177
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ITPR1 CL E G H	3708	6180	OMIM:117360	Spinocerebellar ataxia 29		177
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	JAM3 CL E G H	83700	15532	OMIM:613730	Hemorrhagic destruction of the brain, subependymal calcification,and cataracts	HP:0040283 - Occasional	4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KATNIP CL E G H	23247	29068	ORPHA:475	Joubert syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KATNIP CL E G H	23247	29068	OMIM:616784	JOUBERT SYNDROME 26; JBTS26
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KCNQ1 CL E G H	3784	6294	OMIM:130650	Beckwith-Wiedemann syndrome		730
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KCNQ1OT1 CL E G H	10984	6295	OMIM:130650	Beckwith-Wiedemann syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIAA0586 CL E G H	9786	19960	ORPHA:475	Joubert syndrome		24
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIAA0586 CL E G H	9786	19960	ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	HP:0040282 - Frequent	24
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIAA0586 CL E G H	9786	19960	OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly		24
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIAA0753 CL E G H	9851	29110	OMIM:619476	JOUBERT SYNDROME 38; JBTS38		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIAA0753 CL E G H	9851	29110	ORPHA:2754	Orofaciodigital syndrome type 6		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIDINS220 CL E G H	57498	29508	OMIM:619501	VENTRICULOMEGALY AND ARTHROGRYPOSIS; VENARG		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIF14 CL E G H	9928	19181	OMIM:616258	Meckel syndrome 12	.	9
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIF7 CL E G H	374654	30497	ORPHA:36	Acrocallosal syndrome		167
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KIF7 CL E G H	374654	30497	ORPHA:2754	Orofaciodigital syndrome type 6		167
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KMT2C CL E G H	58508	13726	ORPHA:261652	Kleefstra syndrome due to a point mutation	HP:0040283 - Occasional	99
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	KRAS CL E G H	3845	6407	ORPHA:2612	Linear nevus sebaceus syndrome		196
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	L1CAM CL E G H	3897	6470	OMIM:304100	Corpus callosum, partial agenesis of, X-linked	.	134
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	L1CAM CL E G H	3897	6470	ORPHA:1497	X-linked complicated corpus callosum dysgenesis	HP:0040282 - Frequent	134
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LAMA1 CL E G H	284217	6481	ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		35
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LAMA1 CL E G H	284217	6481	OMIM:615960	Poretti-Boltshauser syndrome		35
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LAMB1 CL E G H	3912	6486	ORPHA:352682	Cobblestone lissencephaly without muscular or ocular involvement	HP:0040282 - Frequent	71
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LAMB1 CL E G H	3912	6486	OMIM:615191	Lissencephaly 5		71
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LARGE1 CL E G H	9215	6511	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	136
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LARGE1 CL E G H	9215	6511	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		136
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LARGE1 CL E G H	9215	6511	OMIM:613154	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6		136
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LARGE1 CL E G H	9215	6511	OMIM:608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6	.	136
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LARGE1 CL E G H	9215	6511	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	136
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LETM1 CL E G H	3954	6556	OMIM:620089			2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	LRRC32 CL E G H	2615	4161	OMIM:619074	CLEFT PALATE, PROLIFERATIVE RETINOPATHY, AND DEVELOPMENTAL DELAY; CPPRDD
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAB21L1 CL E G H	4081	6757	OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome	.
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MACF1 CL E G H	23499	13664	OMIM:618325	Lissencephaly 9 with complex brainstem malformation	.	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAN1B1 CL E G H	11253	6823	ORPHA:397941	MAN1B1-CDG	HP:0040283 - Occasional	93
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAN1B1 CL E G H	11253	6823	OMIM:614202	Rafiq syndrome		93
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAN2C1 CL E G H	4123	6827	OMIM:619775	CONGENITAL DISORDER OF DEGLYCOSYLATION 2; CDDG2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAP2K2 CL E G H	5605	6842	OMIM:615280	Cardiofaciocutaneous syndrome 4	.	178
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAPK8IP3 CL E G H	23162	6884	OMIM:618443	Neurodevelopmental disorder with or without variable brain abnormalities	.
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAPKAPK5 CL E G H	8550	6889	OMIM:619869
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MARS2 CL E G H	92935	25133	ORPHA:314603	Autosomal recessive spastic ataxia with leukoencephalopathy	HP:0040281 - Very frequent	25
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MAST1 CL E G H	22983	19034	OMIM:618273	Mega-Corpus-Callosum syndrome with cerebellar hypoplasia and cortical malformations	.	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MBD5 CL E G H	55777	20444	OMIM:156200	Mental retardation, autosomal dominant 1		252
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MBTPS2 CL E G H	51360	15455	ORPHA:2273	Ichthyosis follicularis-alopecia-photophobia syndrome	HP:0040283 - Occasional	22
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MDH1 CL E G H	4190	6970	OMIM:618959	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88; DEE88
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MFSD2A CL E G H	84879	25897	OMIM:616486	Microcephaly 15, primary, autosomal recessive	.	5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MICOS13 CL E G H	125988	33702	OMIM:618329	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 37; COXPD37
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MID1 CL E G H	4281	7095	ORPHA:2745	Opitz GBBB syndrome		57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MID1 CL E G H	4281	7095	OMIM:300000	Opitz gbbb syndrome, type I		57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MINPP1 CL E G H	9562	7102	ORPHA:284339	Pontocerebellar hypoplasia type 7		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MINPP1 CL E G H	9562	7102	OMIM:619527	PONTOCEREBELLAR HYPOPLASIA, TYPE 16; PCH16		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MKS1 CL E G H	54903	7121	ORPHA:475	Joubert syndrome		127
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MKS1 CL E G H	54903	7121	ORPHA:220493	Joubert syndrome with ocular defect		127
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MKS1 CL E G H	54903	7121	ORPHA:564	Meckel syndrome		127
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MKS1 CL E G H	54903	7121	OMIM:249000	Meckel syndrome 1	.	127
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MLXIPL CL E G H	51085	12744	OMIM:194050	Williams-Beuren syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MPL CL E G H	4352	7217	OMIM:604498	Amegakaryocytic thrombocytopenia, congenital		97
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MRE11 CL E G H	4361	7230	ORPHA:251347	Ataxia-telangiectasia-like disorder		532
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MSTO1 CL E G H	55154	29678	ORPHA:502423	Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome	HP:0040282 - Frequent
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MTM1 CL E G H	4534	7448	OMIM:310400	Myopathy, centronuclear, X-linked		185
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MUSK CL E G H	4593	7525	OMIM:208150	Fetal akinesia deformation sequence	.	72
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MUSK CL E G H	4593	7525	ORPHA:994	Fetal akinesia deformation sequence		72
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MYO5A CL E G H	4644	7602	ORPHA:33445	Neuroectodermal melanolysosomal disease	HP:0040283 - Occasional	35
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	MYOD1 CL E G H	4654	7611	ORPHA:994	Fetal akinesia deformation sequence
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NCAPG2 CL E G H	54892	21904	OMIM:618460	Khan-Khan-Katsanis syndrome		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NDE1 CL E G H	54820	17619	OMIM:614019	Lissencephaly 4	.	96
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NDE1 CL E G H	54820	17619	OMIM:605013	MICROHYDRANENCEPHALY	.	96
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NDUFA6 CL E G H	4700	7690	OMIM:618253	Mitochondrial complex I deficiency, nuclear type 33	.	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NEK1 CL E G H	4750	7744	OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly		101
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NFIX CL E G H	4784	7788	ORPHA:561	Marshall-Smith syndrome	HP:0040283 - Occasional	40
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NFIX CL E G H	4784	7788	OMIM:602535	Marshall-Smith syndrome		40
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NODAL CL E G H	4838	7865	OMIM:270100	Heterotaxy, visceral, 5		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NONO CL E G H	4841	7871	ORPHA:466791	Macrocephaly-intellectual disability-left ventricular non compaction syndrome	HP:0040283 - Occasional	10
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NONO CL E G H	4841	7871	OMIM:300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		10
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NPHP1 CL E G H	4867	7905	OMIM:609583	Joubert syndrome 4		85
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NPHP1 CL E G H	4867	7905	ORPHA:220497	Joubert syndrome with renal defect		85
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NPHP3 CL E G H	27031	7907	OMIM:267010	MECKEL SYNDROME, TYPE 7; MKS7		157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NPHP3 CL E G H	27031	7907	ORPHA:3032	NPHP3-related Meckel-like syndrome		157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NPHP3 CL E G H	27031	7907	OMIM:208540	Renal-Hepatic-Pancreatic dysplasia		157
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NRAS CL E G H	4893	7989	ORPHA:2612	Linear nevus sebaceus syndrome		102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NRAS CL E G H	4893	7989	OMIM:249400	Neurocutaneous melanosis, somatic		102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NSD1 CL E G H	64324	14234	ORPHA:821	Sotos syndrome		544
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NSRP1 CL E G H	84081	25305	OMIM:620001
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NUP37 CL E G H	79023	29929	OMIM:618179	Microcephaly 24, primary, autosomal recessive
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	NUP88 CL E G H	4927	8067	ORPHA:994	Fetal akinesia deformation sequence
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OCLN CL E G H	100506658	8104	OMIM:251290	Band-Like calcification with simplified gyration and polymicrogyria	.	23
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OFD1 CL E G H	8481	2567	OMIM:300804	Joubert syndrome 10		201
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OFD1 CL E G H	8481	2567	ORPHA:2750	Orofaciodigital syndrome type 1		201
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OFD1 CL E G H	8481	2567	ORPHA:2754	Orofaciodigital syndrome type 6		201
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OPHN1 CL E G H	4983	8148	OMIM:300486	Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance		55
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OPHN1 CL E G H	4983	8148	ORPHA:137831	X-linked intellectual disability-cerebellar hypoplasia syndrome	HP:0040281 - Very frequent	55
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OTUD5 CL E G H	55593	25402	OMIM:301056	MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	OXR1 CL E G H	55074	15822	OMIM:213000	Cerebellar hypoplasia	.	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PACS1 CL E G H	55690	30032	ORPHA:329224	Intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome	HP:0040283 - Occasional	24
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PACS1 CL E G H	55690	30032	OMIM:615009	Schuurs-Hoeijmakers syndrome	HP:0040283 - Occasional	24
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PAFAH1B1 CL E G H	5048	8574	OMIM:607432	Lissencephaly 1	.	231
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PAFAH1B1 CL E G H	5048	8574	ORPHA:95232	Lissencephaly due to LIS1 mutation		231
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PARN CL E G H	5073	8609	OMIM:616353	Dyskeratosis congenita, autosomal recessive 6	.	26
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PARN CL E G H	5073	8609	ORPHA:3322	Hoyeraal-Hreidarsson syndrome	HP:0040281 - Very frequent	26
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PCGF2 CL E G H	7703	12929	OMIM:618371	Turnpenny-Fry syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PCLO CL E G H	27445	13406	OMIM:608027	Pontocerebellar hypoplasia, type 3	.	6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PDE6D CL E G H	5147	8788	ORPHA:2754	Orofaciodigital syndrome type 6		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PDHB CL E G H	5162	8808	ORPHA:255138	Pyruvate dehydrogenase E1-beta deficiency	HP:0040283 - Occasional	37
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PGAP1 CL E G H	80055	25712	OMIM:615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		20
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PHGDH CL E G H	26227	8923	OMIM:256520	Neu-Laxova syndrome	.	37
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PI4KA CL E G H	5297	8983	ORPHA:98889	Bilateral perisylvian polymicrogyria		11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PI4KA CL E G H	5297	8983	OMIM:619708	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME 2; GIDID2		11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PI4KA CL E G H	5297	8983	OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis	.	11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIBF1 CL E G H	10464	23352	ORPHA:475	Joubert syndrome		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIEZO2 CL E G H	63895	26270	OMIM:248700	Marden-Walker syndrome	.	77
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIEZO2 CL E G H	63895	26270	ORPHA:2461	Marden-Walker syndrome	HP:0040283 - Occasional	77
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIGA CL E G H	5277	8957	OMIM:300868	Multiple congenital anomalies-hypotonia-seizures syndrome 2	.	46
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIGG CL E G H	54872	25985	ORPHA:488635	Early-onset epilepsy-intellectual disability-brain anomalies syndrome	HP:0040282 - Frequent	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIGG CL E G H	54872	25985	OMIM:616917	Mental retardation, autosomal recessive 53	.	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIGN CL E G H	23556	8967	ORPHA:2059	Fryns syndrome		37
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIGT CL E G H	51604	14938	OMIM:615398	Multiple congenital anomalies-hypotonia-seizures syndrome 3	.	12
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PIGU CL E G H	128869	15791	OMIM:618590	NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES, SEIZURES, AND SCOLIOSIS; NEDBSS
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PLCH1 CL E G H	23007	29185	OMIM:619895
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PLG CL E G H	5340	9071	ORPHA:722	Hypoplasminogenemia		11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PLG CL E G H	5340	9071	OMIM:217090	Plasminogen deficiency, type iligneous conjunctivitis, included	.	11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PLP1 CL E G H	5354	9086	ORPHA:280210	Pelizaeus-Merzbacher disease, connatal form	HP:0040283 - Occasional	60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PMM2 CL E G H	5373	9115	OMIM:212065	Congenital disorder of glycosylation, type Ia		150
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PMM2 CL E G H	5373	9115	ORPHA:79318	PMM2-CDG	HP:0040282 - Frequent	150
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PMPCA CL E G H	23203	18667	OMIM:213200	Spinocerebellar ataxia, autosomal recessive 2	.	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POLR3A CL E G H	11128	30074	ORPHA:447896	Tremor-ataxia-central hypomyelination syndrome	HP:0040282 - Frequent	138
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POLR3A CL E G H	11128	30074	OMIM:264090	Wiedemann-Rautenstrauch syndrome		138
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POLR3A CL E G H	11128	30074	ORPHA:3455	Wiedemann-Rautenstrauch syndrome	HP:0040283 - Occasional	138
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMGNT1 CL E G H	55624	19139	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040282 - Frequent	180
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMGNT1 CL E G H	55624	19139	OMIM:253280	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3	.	180
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMGNT1 CL E G H	55624	19139	OMIM:613151	Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3	.	180
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMGNT1 CL E G H	55624	19139	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	180
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMGNT2 CL E G H	84892	25902	OMIM:614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8	.	33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMGNT2 CL E G H	84892	25902	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMK CL E G H	84197	26267	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040282 - Frequent	18
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMK CL E G H	84197	26267	OMIM:615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12	HP:0040283 - Occasional	18
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMK CL E G H	84197	26267	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	18
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT1 CL E G H	10585	9202	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040282 - Frequent	213
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT1 CL E G H	10585	9202	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	213
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT1 CL E G H	10585	9202	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		213
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT1 CL E G H	10585	9202	OMIM:613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1	.	213
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT1 CL E G H	10585	9202	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	213
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT2 CL E G H	29954	19743	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040282 - Frequent	221
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT2 CL E G H	29954	19743	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	221
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT2 CL E G H	29954	19743	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		221
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT2 CL E G H	29954	19743	OMIM:613150	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2		221
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT2 CL E G H	29954	19743	OMIM:613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2	.	221
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POMT2 CL E G H	29954	19743	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent	221
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	POU4F1 CL E G H	5457	9218	ORPHA:314647	Non-progressive cerebellar ataxia with intellectual disability	HP:0040282 - Frequent
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PPFIBP1 CL E G H	8496	9249	OMIM:620024
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PPIL1 CL E G H	51645	9260	OMIM:619301	PONTOCEREBELLAR HYPOPLASIA, TYPE 14; PCH14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PPP1CB CL E G H	5500	9282	OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		9
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PPP1R15B CL E G H	84919	14951	ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome	HP:0040283 - Occasional	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PPP1R21 CL E G H	129285	30595	OMIM:619383	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PPP2R1A CL E G H	5518	9302	ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome		13
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PRDM13 CL E G H	59336	13998	OMIM:619909			2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PRDM13 CL E G H	59336	13998	OMIM:619761	CEREBELLAR DYSFUNCTION, IMPAIRED INTELLECTUAL DEVELOPMENT, AND HYPOGONADOTROPIC HYPOGONADISM; CDIDHH		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PRKDC CL E G H	5591	9413	OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities		42
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PSAT1 CL E G H	29968	19129	OMIM:616038	Neu-Laxova syndrome 2		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PSAT1 CL E G H	29968	19129	OMIM:610992	Phosphoserine aminotransferase deficiency		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PSAT1 CL E G H	29968	19129	ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PTEN CL E G H	5728	9588	ORPHA:101070	Bilateral frontoparietal polymicrogyria		948
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PTF1A CL E G H	256297	23734	OMIM:609069	Pancreatic and cerebellar agenesis	.	22
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PTF1A CL E G H	256297	23734	ORPHA:65288	Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome	HP:0040281 - Very frequent	22
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	PTRH2 CL E G H	51651	24265	ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease		6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAB11B CL E G H	9230	9761	OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAB18 CL E G H	22931	14244	ORPHA:2510	Micro syndrome		85
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAB3GAP1 CL E G H	22930	17063	ORPHA:2510	Micro syndrome		90
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAB3GAP1 CL E G H	22930	17063	OMIM:600118	Warburg micro syndrome 1		90
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAB3GAP2 CL E G H	25782	17168	ORPHA:2510	Micro syndrome		135
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAC1 CL E G H	5879	9801	OMIM:617751	Mental retardation, autosomal dominant 48	.	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAC1 CL E G H	5879	9801	ORPHA:500159	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom	HP:0040283 - Occasional	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RAPSN CL E G H	5913	9863	ORPHA:994	Fetal akinesia deformation sequence		73
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RARS2 CL E G H	57038	21406	OMIM:611523	Pontocerebellar hypoplasia, type 6	.	93
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RBBP8 CL E G H	5932	9891	OMIM:606744	Seckel syndrome 2		68
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RBM10 CL E G H	8241	9896	OMIM:311900	Tarp syndrome	.	16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RBM10 CL E G H	8241	9896	ORPHA:2886	TARP syndrome	HP:0040283 - Occasional	16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RBM8A CL E G H	9939	9905	OMIM:274000	Thrombocytopenia-absent radius syndrome		10
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RELN CL E G H	5649	9957	OMIM:257320	Lissencephaly 2		334
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RERE CL E G H	473	9965	OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RERE CL E G H	473	9965	ORPHA:494344	RERE-related neurodevelopmental syndrome		16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RHOBTB2 CL E G H	23221	18756	OMIM:618004	Epileptic encephalopathy, early infantile, 64	.	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RNF113A CL E G H	7737	12974	OMIM:300953	Trichothiodystrophy 5, nonphotosensitive	.	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RNU4ATAC CL E G H	100151683	34016	OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		15
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ROBO3 CL E G H	64221	13433	OMIM:607313	Gaze palsy, familial horizontal, with progressive scoliosis, 1	.	90
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ROGDI CL E G H	79641	29478	OMIM:226750	Kohlschutter-Tonz syndrome	.	57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RORA CL E G H	6095	10258	OMIM:618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPE65 CL E G H	6121	10294	OMIM:204100	Leber congenital amaurosis, type II		129
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPGRIP1 CL E G H	57096	13436	ORPHA:564	Meckel syndrome		109
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPGRIP1L CL E G H	23322	29168	ORPHA:1454	Joubert syndrome with hepatic defect		167
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPGRIP1L CL E G H	23322	29168	ORPHA:220497	Joubert syndrome with renal defect		167
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPGRIP1L CL E G H	23322	29168	ORPHA:564	Meckel syndrome		167
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPL10 CL E G H	6134	10298	OMIM:300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		10
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RPL10 CL E G H	6134	10298	ORPHA:459070	X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome	HP:0040282 - Frequent	10
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RTEL1 CL E G H	51750	15888	OMIM:615190	Dyskeratosis congenita, autosomal recessive 5	HP:0040281 - Very frequent	77
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RTEL1 CL E G H	51750	15888	ORPHA:3322	Hoyeraal-Hreidarsson syndrome	HP:0040281 - Very frequent	77
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RTTN CL E G H	25914	18654	ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency	HP:0040283 - Occasional	113
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	RXYLT1 CL E G H	10329	13530	ORPHA:899	Walker-Warburg syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SACS CL E G H	26278	10519	ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay		309
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SASS6 CL E G H	163786	25403	OMIM:616402	Microcephaly 14, primary, autosomal recessive	HP:0040283 - Occasional	4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SEMA3E CL E G H	9723	10727	ORPHA:138	CHARGE syndrome		16
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SEMA6B CL E G H	10501	10739	OMIM:618876	EPILEPSY, PROGRESSIVE MYOCLONIC, 11; EPM11
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SEPSECS CL E G H	51091	30605	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	66
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SETD2 CL E G H	29072	18420	ORPHA:821	Sotos syndrome		60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SHQ1 CL E G H	55164	25543	OMIM:619922
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SIL1 CL E G H	64374	24624	ORPHA:559	Marinesco-Sjögren syndrome	HP:0040281 - Very frequent	67
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SIX3 CL E G H	6496	10889	OMIM:157170	Holoprosencephaly 2	.	32
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC18A3 CL E G H	6572	10936	ORPHA:994	Fetal akinesia deformation sequence		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC1A3 CL E G H	6507	10941	OMIM:612656	Episodic ataxia, type 6	.	63
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC25A1 CL E G H	6576	10979	OMIM:615182	Combined d-2- and l-2-hydroxyglutaric aciduria	.	28
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC25A19 CL E G H	60386	14409	ORPHA:99742	Amish lethal microcephaly		36
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC25A19 CL E G H	60386	14409	OMIM:607196	Microcephaly, Amish type	.	36
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC25A24 CL E G H	29957	20662	OMIM:612289	Fontaine progeroid syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC25A46 CL E G H	91137	25198	OMIM:619303	PONTOCEREBELLAR HYPOPLASIA, TYPE 1E; PCH1E		14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC35A2 CL E G H	7355	11022	OMIM:300896	Congenital disorder of glycosylation, type IIm		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SLC35A2 CL E G H	7355	11022	ORPHA:356961	SLC35A2-CDG		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCA4 CL E G H	6597	11100	ORPHA:1465	Coffin-Siris syndrome		617
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCA4 CL E G H	6597	11100	OMIM:614609	Coffin-Siris syndrome 4		617
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCB1 CL E G H	6598	11103	ORPHA:1465	Coffin-Siris syndrome		87
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCB1 CL E G H	6598	11103	OMIM:614608	Coffin-Siris syndrome 3		87
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCC2 CL E G H	6601	11105	ORPHA:1465	Coffin-Siris syndrome		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCD1 CL E G H	6602	11106	ORPHA:1465	Coffin-Siris syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCE1 CL E G H	6605	11109	ORPHA:1465	Coffin-Siris syndrome		47
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMARCE1 CL E G H	6605	11109	OMIM:616938	Coffin-Siris syndrome 5	.	47
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMG9 CL E G H	56006	25763	OMIM:616920	Heart and brain malformation syndrome		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SMPD4 CL E G H	55627	32949	OMIM:618622	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES; NEDMABA		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SNX14 CL E G H	57231	14977	OMIM:616354	Spinocerebellar ataxia, autosomal recessive 20	.	14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SON CL E G H	6651	11183	ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome		12
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SON CL E G H	6651	11183	OMIM:617140	Zttk syndrome	.	12
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SOX11 CL E G H	6664	11191	ORPHA:1465	Coffin-Siris syndrome		14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SOX4 CL E G H	6659	11200	ORPHA:1465	Coffin-Siris syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SRD5A3 CL E G H	79644	25812	OMIM:612379	Congenital disorder of glycosylation, type IQ		80
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SRPX2 CL E G H	27286	30668	ORPHA:98889	Bilateral perisylvian polymicrogyria		50
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	STAG2 CL E G H	10735	11355	ORPHA:521258	Xq25 microduplication syndrome	HP:0040282 - Frequent	1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	STAT2 CL E G H	6773	11363	OMIM:618886	PSEUDO-TORCH SYNDROME 3; PTORCH3		9
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	STUB1 CL E G H	10273	11427	ORPHA:412057	Autosomal recessive cerebellar ataxia due to STUB1 deficiency	HP:0040283 - Occasional	14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	STUB1 CL E G H	10273	11427	OMIM:615768	Spinocerebellar ataxia, autosomal recessive 16	.	14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SUFU CL E G H	51684	16466	ORPHA:475	Joubert syndrome		124
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SUOX CL E G H	6821	11460	OMIM:272300	SULFOCYSTEINURIA		40
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	SYT2 CL E G H	127833	11510	OMIM:619461	MYASTHENIC SYNDROME, CONGENITAL, 7B, PRESYNAPTIC, AUTOSOMAL RECESSIVE; CMS7B		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TAF1 CL E G H	6872	11535	OMIM:300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33; MRXS33		21
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TAPT1 CL E G H	202018	26887	OMIM:616897	Osteochondrodysplasia, complex lethal, Symoens-Barnes-Gistelinck type		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TBC1D20 CL E G H	128637	16133	ORPHA:2510	Micro syndrome		15
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TBC1D24 CL E G H	57465	29203	ORPHA:79500	DOORS syndrome		271
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TBC1D24 CL E G H	57465	29203	OMIM:220500	Doors syndrome		271
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TBCK CL E G H	93627	28261	OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3	.	13
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN1 CL E G H	79600	26113	ORPHA:475	Joubert syndrome		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN1 CL E G H	79600	26113	OMIM:614173	Joubert syndrome 13		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN1 CL E G H	79600	26113	ORPHA:564	Meckel syndrome		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN2 CL E G H	79867	25774	ORPHA:475	Joubert syndrome		76
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN2 CL E G H	79867	25774	OMIM:616654	Joubert syndrome 24	.	76
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN2 CL E G H	79867	25774	ORPHA:564	Meckel syndrome		76
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN3 CL E G H	26123	24519	ORPHA:564	Meckel syndrome		31
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TCTN3 CL E G H	26123	24519	ORPHA:2754	Orofaciodigital syndrome type 6		31
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TERC CL E G H	7012	11727	OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1	.	48
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TERT CL E G H	7015	11730	OMIM:613989	Dyskeratosis congenita, autosomal dominant 2	.	238
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TERT CL E G H	7015	11730	OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1	.	238
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TERT CL E G H	7015	11730	ORPHA:3322	Hoyeraal-Hreidarsson syndrome	HP:0040281 - Very frequent	238
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	THG1L CL E G H	54974	26053	OMIM:618800	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 28; SCAR28
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	THOC2 CL E G H	57187	19073	OMIM:300957	Mental retardation, X-linked 12/35		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TINF2 CL E G H	26277	11824	OMIM:613990	Dyskeratosis congenita, autosomal dominant 3	.	60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TINF2 CL E G H	26277	11824	OMIM:127550	Dyskeratosis congenita, autosomal dominant, 1	.	60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TINF2 CL E G H	26277	11824	ORPHA:3322	Hoyeraal-Hreidarsson syndrome	HP:0040281 - Very frequent	60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TINF2 CL E G H	26277	11824	OMIM:268130	Revesz syndrome	.	60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TKFC CL E G H	26007	24552	OMIM:618805	TRIOKINASE AND FMN CYCLASE DEFICIENCY SYNDROME; TKFCD
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMCO1 CL E G H	54499	18188	ORPHA:1394	Cerebrofaciothoracic dysplasia		6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM107 CL E G H	84314	28128	ORPHA:564	Meckel syndrome		4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM107 CL E G H	84314	28128	OMIM:617562	Meckel syndrome 13	.	4
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM138 CL E G H	51524	26944	OMIM:614465	JOUBERT SYNDROME 16; JBTS16		39
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM138 CL E G H	51524	26944	ORPHA:2318	Joubert syndrome with oculorenal defect		39
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM216 CL E G H	51259	25018	ORPHA:2318	Joubert syndrome with oculorenal defect		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM216 CL E G H	51259	25018	ORPHA:564	Meckel syndrome		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM216 CL E G H	51259	25018	OMIM:603194	Meckel syndrome, type 2		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM216 CL E G H	51259	25018	ORPHA:2754	Orofaciodigital syndrome type 6		45
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM218 CL E G H	219854	27344	ORPHA:475	Joubert syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM218 CL E G H	219854	27344	OMIM:619562	JOUBERT SYNDROME 39; JBTS39
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM231 CL E G H	79583	37234	ORPHA:2318	Joubert syndrome with oculorenal defect		33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM231 CL E G H	79583	37234	ORPHA:564	Meckel syndrome		33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM231 CL E G H	79583	37234	ORPHA:2752	Orofaciodigital syndrome type 3		33
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM237 CL E G H	65062	14432	ORPHA:475	Joubert syndrome		82
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM237 CL E G H	65062	14432	OMIM:614424	Joubert syndrome 14		82
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM237 CL E G H	65062	14432	ORPHA:2318	Joubert syndrome with oculorenal defect		82
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM237 CL E G H	65062	14432	ORPHA:220497	Joubert syndrome with renal defect		82
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM237 CL E G H	65062	14432	ORPHA:564	Meckel syndrome		82
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM67 CL E G H	91147	28396	OMIM:216360	Coach syndrome 1		166
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM67 CL E G H	91147	28396	ORPHA:475	Joubert syndrome		166
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM67 CL E G H	91147	28396	OMIM:610688	Joubert syndrome 6		166
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM67 CL E G H	91147	28396	ORPHA:1454	Joubert syndrome with hepatic defect		166
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM67 CL E G H	91147	28396	ORPHA:564	Meckel syndrome		166
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMEM67 CL E G H	91147	28396	OMIM:607361	Meckel syndrome 3		166
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TMTC3 CL E G H	160418	26899	OMIM:617255	Lissencephaly 8		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TNPO2 CL E G H	30000	19998	OMIM:619556	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED SPEECH, AND DYSMORPHIC FACIES; IDDHISD
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TOE1 CL E G H	114034	15954	ORPHA:284339	Pontocerebellar hypoplasia type 7		6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TOE1 CL E G H	114034	15954	OMIM:614969	Pontocerebellar hypoplasia, type 7	.	6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TOGARAM1 CL E G H	23116	19959	ORPHA:475	Joubert syndrome
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TOGARAM1 CL E G H	23116	19959	OMIM:619185	JOUBERT SYNDROME 37; JBTS37
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TOPORS CL E G H	10210	21653	ORPHA:2754	Orofaciodigital syndrome type 6		61
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TP53RK CL E G H	112858	16197	OMIM:617730	Galloway-Mowat syndrome 4	.
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TRAPPC9 CL E G H	83696	30832	ORPHA:352530	Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome	HP:0040281 - Very frequent	158
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TRAPPC9 CL E G H	83696	30832	OMIM:613192	Mental retardation, autosomal recessive 13		158
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TRIP13 CL E G H	9319	12307	ORPHA:1052	Mosaic variegated aneuploidy syndrome		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TRMT10A CL E G H	93587	28403	ORPHA:391408	Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome	HP:0040283 - Occasional	7
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TRRAP CL E G H	8295	12347	OMIM:618454	Developmental delay with or without dysmorphic facies and autism		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN15 CL E G H	116461	16791	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN15 CL E G H	116461	16791	OMIM:617026	Pontocerebellar hypoplasia, type 2F		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN2 CL E G H	80746	28422	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	84
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN2 CL E G H	80746	28422	OMIM:612389	Pontocerebellar hypoplasia, type 2B	.	84
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN34 CL E G H	79042	15506	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN34 CL E G H	79042	15506	OMIM:612390	PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		57
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN54 CL E G H	283989	27561	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN54 CL E G H	283989	27561	ORPHA:166063	Pontocerebellar hypoplasia type 4		102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN54 CL E G H	283989	27561	OMIM:277470	Pontocerebellar hypoplasia, type 2A		102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN54 CL E G H	283989	27561	OMIM:225753	Pontocerebellar hypoplasia, type 4		102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TSEN54 CL E G H	283989	27561	OMIM:610204	Pontocerebellar hypoplasia, type 5		102
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBA1A CL E G H	7846	20766	ORPHA:994	Fetal akinesia deformation sequence		106
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBA1A CL E G H	7846	20766	OMIM:611603	Lissencephaly 3		106
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBA1A CL E G H	7846	20766	ORPHA:171680	Lissencephaly due to TUBA1A mutation		106
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBA1A CL E G H	7846	20766	ORPHA:467166	Tubulinopathy-associated dysgyria		106
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBB CL E G H	203068	20778	OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6	.	14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBB CL E G H	203068	20778	OMIM:156610	Skin creases, congenital symmetric circumferential, 1		14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBB2B CL E G H	347733	30829	OMIM:610031	Cortical dysplasia, complex, with other brain malformations 7	.	39
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBB2B CL E G H	347733	30829	ORPHA:467166	Tubulinopathy-associated dysgyria		39
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBB3 CL E G H	10381	20772	ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	HP:0040282 - Frequent	64
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBB3 CL E G H	10381	20772	ORPHA:467166	Tubulinopathy-associated dysgyria		64
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TUBGCP6 CL E G H	85378	18127	OMIM:251270	Microcephaly and chorioretinopathy, autosomal recessive, 1	.	61
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TWIST1 CL E G H	7291	12428	OMIM:617746	Sweeney-Cox syndrome	.	18
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	TXNDC15 CL E G H	79770	20652	ORPHA:564	Meckel syndrome		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	UFSP2 CL E G H	55325	25640	OMIM:620028			2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	USP18 CL E G H	11274	12616	OMIM:617397	Pseudo-Torch syndrome 2	.	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	USP9X CL E G H	8239	12632	OMIM:300968	Mental retardation, X-linked 99, syndromic, female-restricted		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	USP9X CL E G H	8239	12632	ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability	HP:0040283 - Occasional	27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VAC14 CL E G H	55697	25507	ORPHA:3472	Yunis-Varon syndrome	HP:0040283 - Occasional	6
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VARS2 CL E G H	57176	21642	OMIM:615917	Combined oxidative phosphorylation deficiency 20		56
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VLDLR CL E G H	7436	12698	OMIM:224050	Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1	.	111
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VPS13B CL E G H	157680	2183	OMIM:216550	Cohen syndrome	.	546
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VPS35L CL E G H	57020	24641	OMIM:619135	RITSCHER-SCHINZEL SYNDROME 3; RTSC3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VPS4A CL E G H	27183	13488	OMIM:619273	CIMDAG SYNDROME; CIMDAG		1
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VPS51 CL E G H	738	1172	OMIM:618606	PONTOCEREBELLAR HYPOPLASIA, TYPE 13; PCH13
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	VRK1 CL E G H	7443	12718	OMIM:607596	Pontocerebellar hypoplasia type 1A	.	32
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WAC CL E G H	51322	17327	ORPHA:284169	Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion	HP:0040283 - Occasional	20
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WARS2 CL E G H	10352	12730	ORPHA:572798	WARS2-related combined oxidative phosphorylation defect		2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WASHC5 CL E G H	9897	28984	ORPHA:7	3C syndrome		83
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WASHC5 CL E G H	9897	28984	OMIM:220210	Ritscher-Schinzel syndrome 1		83
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WDR26 CL E G H	80232	21208	ORPHA:513456	Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome	HP:0040283 - Occasional	8
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WDR35 CL E G H	57539	29250	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional	136
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WDR73 CL E G H	84942	25928	OMIM:251300	Galloway-mowat syndrome 1		14
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WDR81 CL E G H	124997	26600	OMIM:610185	Cerebellar ataxia, mental retardation, and dysequilibrium syndrome2	.	27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WDR81 CL E G H	124997	26600	OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		27
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WLS CL E G H	79971	30238	OMIM:619648	ZAKI SYNDROME; ZKS
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	WNT1 CL E G H	7471	12774	OMIM:615220	Osteogenesis imperfecta, type XV	.	12
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	YME1L1 CL E G H	10730	12843	OMIM:617302	Optic atrophy 11	.	2
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZBTB11 CL E G H	27107	16740	OMIM:618383	Intellectual developmental disorder, autosomal recessive 69	HP:0040284 - Very rare
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZEB2 CL E G H	9839	14881	ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation	HP:0040284 - Very rare	362
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZEB2 CL E G H	9839	14881	ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22	HP:0040284 - Very rare	362
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZIC1 CL E G H	7545	12872	OMIM:616602	Craniosynostosis 6		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZIC1 CL E G H	7545	12872	OMIM:618736	STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS		5
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZIC3 CL E G H	7547	12874	OMIM:306955	Heterotaxy, visceral, 1, X-linked		39
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZNF292 CL E G H	23036	18410	OMIM:619188	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 64; MRD64		3
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZNF335 CL E G H	63925	15807	OMIM:615095	Microcephaly 10, primary, autosomal recessive		60
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZNF423 CL E G H	23090	16762	ORPHA:2318	Joubert syndrome with oculorenal defect		49
HP:0001321	HP:0001321	Cerebellar hypoplasia	0	ZNF423 CL E G H	23090	16762	OMIM:614844	Nephronophthisis 14		49
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ADGRG1 CL E G H	9289	4512	ORPHA:101070	Bilateral frontoparietal polymicrogyria	HP:0040282 - Frequent	88
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ADGRG1 CL E G H	9289	4512	ORPHA:98889	Bilateral perisylvian polymicrogyria	HP:0040283 - Occasional	88
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	AFF3 CL E G H	3899	6473	OMIM:619297	KINSSHIP SYNDROME; KINS		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	AHI1 CL E G H	54806	21575	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	175
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	AHI1 CL E G H	54806	21575	OMIM:608629	Joubert syndrome 3	.	175
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	AHI1 CL E G H	54806	21575	ORPHA:220493	Joubert syndrome with ocular defect	HP:0040281 - Very frequent	175
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ALG3 CL E G H	10195	23056	ORPHA:79321	ALG3-CDG		37
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ALX4 CL E G H	60529	450	OMIM:613451	Frontonasal dysplasia 2	.	132
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	AP1S2 CL E G H	8905	560	OMIM:304340	Pettigrew syndrome		13
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	APC2 CL E G H	10297	24036	ORPHA:821	Sotos syndrome	HP:0040283 - Occasional	1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARHGEF2 CL E G H	9181	682	OMIM:617523	Neurodevelopmental disorder with midbrain and hindbrain malformations		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARID1A CL E G H	8289	11110	ORPHA:1465	Coffin-Siris syndrome		88
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARID1A CL E G H	8289	11110	OMIM:614607	Coffin-Siris syndrome 2		88
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARID1B CL E G H	57492	18040	ORPHA:1465	Coffin-Siris syndrome		219
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARID1B CL E G H	57492	18040	OMIM:135900	Coffin-Siris syndrome 1		219
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARID2 CL E G H	196528	18037	ORPHA:1465	Coffin-Siris syndrome		25
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARL13B CL E G H	200894	25419	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	62
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARL3 CL E G H	403	694	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARL3 CL E G H	403	694	OMIM:618161	JOUBERT SYNDROME 35; JBTS35		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARMC9 CL E G H	80210	20730	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ARMC9 CL E G H	80210	20730	OMIM:617622	JOUBERT SYNDROME 30; JBTS30
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ASXL1 CL E G H	171023	18318	ORPHA:97297	Bohring-Opitz syndrome		145
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ASXL1 CL E G H	171023	18318	OMIM:605039	Bohring-Opitz syndrome		145
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ASXL3 CL E G H	80816	29357	ORPHA:352577	Bainbridge-Ropers syndrome	HP:0040283 - Occasional	49
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ASXL3 CL E G H	80816	29357	OMIM:615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		49
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATN1 CL E G H	1822	3033	OMIM:618494	Congenital hypotonia, epilepsy, developmental delay, and digital anomalies	.	16
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP2B3 CL E G H	492	816	ORPHA:314978	X-linked non progressive cerebellar ataxia	HP:0040282 - Frequent	19
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP6V0A2 CL E G H	23545	18481	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		140
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP6V0A2 CL E G H	23545	18481	OMIM:219200	Cutis laxa, autosomal recessive, type IIA		140
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP6V0A2 CL E G H	23545	18481	ORPHA:2834	Wrinkly skin syndrome	HP:0040282 - Frequent	140
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP6V1A CL E G H	523	851	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP6V1B2 CL E G H	526	854	ORPHA:79500	DOORS syndrome		5
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATP6V1E1 CL E G H	529	857	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type		2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ATR CL E G H	545	882	OMIM:210600	Seckel syndrome 1	.	168
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	ATXN2 CL E G H	6311	10555	ORPHA:98756	Spinocerebellar ataxia type 2	HP:0040282 - Frequent	11
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B3GALNT2 CL E G H	148789	28596	ORPHA:899	Walker-Warburg syndrome		43
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B4GALT1 CL E G H	2683	924	ORPHA:79332	B4GALT1-CDG		85
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B4GALT1 CL E G H	2683	924	OMIM:607091	Congenital disorder of glycosylation, type IID		85
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	B4GAT1 CL E G H	11041	15685	OMIM:615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13		17
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B4GAT1 CL E G H	11041	15685	OMIM:615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13		17
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B4GAT1 CL E G H	11041	15685	ORPHA:899	Walker-Warburg syndrome		17
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B9D1 CL E G H	27077	24123	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	28
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B9D1 CL E G H	27077	24123	ORPHA:564	Meckel syndrome		28
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B9D2 CL E G H	80776	28636	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	34
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B9D2 CL E G H	80776	28636	ORPHA:564	Meckel syndrome		34
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	B9D2 CL E G H	80776	28636	OMIM:614175	Meckel syndrome, type 10		34
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BCOR CL E G H	54880	20893	OMIM:300166	Microphthalmia, syndromic 2		101
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BMP4 CL E G H	652	1071	ORPHA:139471	Microphthalmia with brain and digit anomalies		38
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BMP4 CL E G H	652	1071	OMIM:607932	Microphthalmia, syndromic 6		38
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BRF1 CL E G H	2972	11551	ORPHA:444072	Cerebellar-facial-dental syndrome		7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BUB1 CL E G H	699	1148	ORPHA:1052	Mosaic variegated aneuploidy syndrome		5
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BUB1B CL E G H	701	1149	ORPHA:1052	Mosaic variegated aneuploidy syndrome		76
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BUB1B CL E G H	701	1149	OMIM:257300	Mosaic variegated aneuploidy syndrome 1		76
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	BUB3 CL E G H	9184	1151	ORPHA:1052	Mosaic variegated aneuploidy syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	C2CD3 CL E G H	26005	24564	ORPHA:434179	Orofaciodigital syndrome type 14		27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	C2CD3 CL E G H	26005	24564	OMIM:615948	Orofaciodigital syndrome XIV		27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CBY1 CL E G H	25776	1307	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CC2D2A CL E G H	57545	29253	OMIM:619111	COACH SYNDROME 2; COACH2		247
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CC2D2A CL E G H	57545	29253	ORPHA:1454	Joubert syndrome with hepatic defect	HP:0040281 - Very frequent	247
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CC2D2A CL E G H	57545	29253	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	247
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CC2D2A CL E G H	57545	29253	ORPHA:564	Meckel syndrome		247
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CCDC22 CL E G H	28952	28909	ORPHA:7	3C syndrome		33
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CCDC22 CL E G H	28952	28909	OMIM:300963	Ritscher-Schinzel syndrome 2		33
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CCDC32 CL E G H	90416	28295	OMIM:619123	CARDIOFACIONEURODEVELOPMENTAL SYNDROME; CFNDS		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CDC42 CL E G H	998	1736	ORPHA:487796	Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome		6
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CDC42BPB CL E G H	9578	1738	OMIM:619841
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CDKN1C CL E G H	1028	1786	OMIM:130650	Beckwith-Wiedemann syndrome		114
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CENPF CL E G H	1063	1857	OMIM:243605	Stromme syndrome		27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP104 CL E G H	9731	24866	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	5
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP120 CL E G H	153241	26690	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP120 CL E G H	153241	26690	ORPHA:220493	Joubert syndrome with ocular defect	HP:0040281 - Very frequent	7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP120 CL E G H	153241	26690	OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly		7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP164 CL E G H	22897	29182	OMIM:614845	Nephronophthisis 15	HP:0040283 - Occasional	34
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP290 CL E G H	80184	29021	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	342
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP290 CL E G H	80184	29021	ORPHA:564	Meckel syndrome		342
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP290 CL E G H	80184	29021	OMIM:611134	Meckel syndrome, type 4		342
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP41 CL E G H	95681	12370	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	90
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP41 CL E G H	95681	12370	ORPHA:220493	Joubert syndrome with ocular defect	HP:0040281 - Very frequent	90
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CEP57 CL E G H	9702	30794	ORPHA:1052	Mosaic variegated aneuploidy syndrome		17
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CHD7 CL E G H	55636	20626	ORPHA:138	CHARGE syndrome		515
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	COG1 CL E G H	9382	6545	ORPHA:263508	COG1-CDG	HP:0040282 - Frequent	52
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	COL4A1 CL E G H	1282	2202	ORPHA:899	Walker-Warburg syndrome		193
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CPLANE1 CL E G H	65250	25801	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CPLANE1 CL E G H	65250	25801	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CPLANE1 CL E G H	65250	25801	OMIM:277170	Orofaciodigital syndrome VI	.
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CPSF3 CL E G H	51692	2326	OMIM:619876
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CPT2 CL E G H	1376	2330	ORPHA:228308	Carnitine palmitoyl transferase II deficiency, neonatal form	HP:0040283 - Occasional	101
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CPT2 CL E G H	1376	2330	ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form		101
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CRPPA CL E G H	729920	37276	OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CRPPA CL E G H	729920	37276	ORPHA:899	Walker-Warburg syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CSF1R CL E G H	1436	2433	OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		149
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CSPP1 CL E G H	79848	26193	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	57
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CSPP1 CL E G H	79848	26193	ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	HP:0040283 - Occasional	57
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CSPP1 CL E G H	79848	26193	ORPHA:564	Meckel syndrome		57
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CWF19L1 CL E G H	55280	25613	ORPHA:453521	Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency	HP:0040282 - Frequent	9
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	CWF19L1 CL E G H	55280	25613	OMIM:616127	Spinocerebellar ataxia, autosomal recessive 17		9
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DAG1 CL E G H	1605	2666	ORPHA:370997	Muscle-eye-brain disease with bilateral multicystic leucodystrophy	HP:0040282 - Frequent	108
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DAG1 CL E G H	1605	2666	OMIM:616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9	.	108
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DAG1 CL E G H	1605	2666	ORPHA:899	Walker-Warburg syndrome		108
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DCHS1 CL E G H	8642	13681	ORPHA:314679	Cerebrofacioarticular syndrome	HP:0040283 - Occasional	27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DENND5A CL E G H	23258	19344	OMIM:617281	Epileptic encephalopathy, early infantile, 49		6
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DHCR7 CL E G H	1717	2860	OMIM:270400	Smith-Lemli-Opitz syndrome		159
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DOK7 CL E G H	285489	26594	ORPHA:994	Fetal akinesia deformation sequence		91
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DPF2 CL E G H	5977	9964	ORPHA:1465	Coffin-Siris syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DPH1 CL E G H	1801	3003	ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome	HP:0040282 - Frequent	3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DPH1 CL E G H	1801	3003	OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair	HP:0040283 - Occasional	3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DPH5 CL E G H	51611	24270	OMIM:620070
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DPYSL5 CL E G H	56896	20637	OMIM:619435	RITSCHER-SCHINZEL SYNDROME 4; RTSC4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DYNC1H1 CL E G H	1778	2961	OMIM:614563	Mental retardation, autosomal dominant 13		427
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DYNC2H1 CL E G H	79659	2962	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		304
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DYNC2I1 CL E G H	55112	21862	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	DYNC2I2 CL E G H	89891	28296	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EBF3 CL E G H	253738	19087	OMIM:617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		25
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EBP CL E G H	10682	3133	OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant		51
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EBP CL E G H	10682	3133	ORPHA:401973	MEND syndrome		51
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EBP CL E G H	10682	3133	OMIM:300960	Mend syndrome		51
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EPG5 CL E G H	57724	29331	OMIM:242840	Vici syndrome	.	40
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ESCO2 CL E G H	157570	27230	ORPHA:2319	Juberg-Hayward syndrome		92
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EVC CL E G H	2121	3497	OMIM:225500	Ellis-Van creveld syndrome		209
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EVC2 CL E G H	132884	19747	OMIM:225500	Ellis-Van creveld syndrome		137
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EXOC2 CL E G H	55770	24968	OMIM:619306	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND CEREBELLAR HYPOPLASIA; NEDFACH		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	EXOSC8 CL E G H	11340	17035	OMIM:616081	Pontocerebellar hypoplasia, type 1C	.	4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FAM149B1 CL E G H	317662	29162	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FAR1 CL E G H	84188	26222	ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency		7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FAR1 CL E G H	84188	26222	OMIM:616154	PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER; PFCRD		7
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FAT4 CL E G H	79633	23109	ORPHA:314679	Cerebrofacioarticular syndrome	HP:0040283 - Occasional	114
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FDXR CL E G H	2232	3642	ORPHA:543470	Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome	HP:0040283 - Occasional
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FGFR1 CL E G H	2260	3688	OMIM:613001	Encephalocraniocutaneous lipomatosis		172
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FIG4 CL E G H	9896	16873	OMIM:216340	Yunis-Varon syndrome		111
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	FKRP CL E G H	79147	17997	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040283 - Occasional	157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FKRP CL E G H	79147	17997	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FKRP CL E G H	79147	17997	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FKRP CL E G H	79147	17997	OMIM:613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5		157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FKRP CL E G H	79147	17997	ORPHA:899	Walker-Warburg syndrome		157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FKTN CL E G H	2218	3622	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		184
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FKTN CL E G H	2218	3622	ORPHA:899	Walker-Warburg syndrome		184
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FLVCR2 CL E G H	55640	20105	OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		47
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FOXC1 CL E G H	2296	3800	OMIM:601631	Anterior segment dysgenesis 3	HP:0040283 - Occasional	63
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FOXC1 CL E G H	2296	3800	OMIM:602482	Axenfeld-rieger syndrome, type 3	.	63
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FRMD4A CL E G H	55691	25491	OMIM:616819	Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FRMD4A CL E G H	55691	25491	ORPHA:466688	Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome	HP:0040282 - Frequent	1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	FTO CL E G H	79068	24678	OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath		70
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GEMIN4 CL E G H	50628	15717	OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GJB2 CL E G H	2706	4284	ORPHA:477	KID syndrome		199
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GJB6 CL E G H	10804	4288	ORPHA:477	KID syndrome		56
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GLI3 CL E G H	2737	4319	ORPHA:36	Acrocallosal syndrome		270
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	GMPPB CL E G H	29925	22932	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040283 - Occasional	34
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GMPPB CL E G H	29925	22932	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	34
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GOT2 CL E G H	2806	4433	OMIM:618721	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 82; DEE82
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GPC3 CL E G H	2719	4451	ORPHA:373	Simpson-Golabi-Behmel syndrome		73
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GPC3 CL E G H	2719	4451	OMIM:312870	Simpson-golabi-behmel syndrome, type 1		73
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GPC4 CL E G H	2239	4452	ORPHA:373	Simpson-Golabi-Behmel syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GPC4 CL E G H	2239	4452	OMIM:312870	Simpson-golabi-behmel syndrome, type 1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GRIA3 CL E G H	2892	4573	ORPHA:364028	X-linked intellectual disability due to GRIA3 mutations	HP:0040283 - Occasional	30
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GRM1 CL E G H	2911	4593	OMIM:614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13; SCAR13		8
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	GTPBP2 CL E G H	54676	4670	OMIM:617988	Jaberi-Elahi syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	H19-ICR CL E G H	105259599		OMIM:130650	Beckwith-Wiedemann syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	H3-3A CL E G H	3020	4764	OMIM:619720	BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 1; BRYLIB1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	HHAT CL E G H	55733	18270	OMIM:600092	Nivelon-Nivelon-Mabille syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	HNRNPH1 CL E G H	3187	5041	OMIM:620083
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	HNRNPR CL E G H	10236	5047	OMIM:620073
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	HRAS CL E G H	3265	5173	ORPHA:2612	Linear nevus sebaceus syndrome		113
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	HYLS1 CL E G H	219844	26558	OMIM:236680	Hydrolethalus syndrome 1		31
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	HYLS1 CL E G H	219844	26558	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	31
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	IFT172 CL E G H	26160	30391	OMIM:615630	Short-Rib thoracic dysplasia 10 with or without polydactyly	HP:0040283 - Occasional	48
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	IFT80 CL E G H	57560	29262	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		65
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	IGF2 CL E G H	3481	5466	OMIM:130650	Beckwith-Wiedemann syndrome		9
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	INPP5E CL E G H	56623	21474	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	111
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	INPP5E CL E G H	56623	21474	OMIM:213300	Joubert syndrome 1	.	111
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	INPP5E CL E G H	56623	21474	ORPHA:1454	Joubert syndrome with hepatic defect	HP:0040281 - Very frequent	111
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	INPP5E CL E G H	56623	21474	ORPHA:220493	Joubert syndrome with ocular defect	HP:0040281 - Very frequent	111
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	INTS1 CL E G H	26173	24555	OMIM:618571	NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES; NDCAGF
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ITPR1 CL E G H	3708	6180	OMIM:117360	Spinocerebellar ataxia 29		177
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KATNIP CL E G H	23247	29068	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KATNIP CL E G H	23247	29068	OMIM:616784	JOUBERT SYNDROME 26; JBTS26
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KCNQ1 CL E G H	3784	6294	OMIM:130650	Beckwith-Wiedemann syndrome		730
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KCNQ1OT1 CL E G H	10984	6295	OMIM:130650	Beckwith-Wiedemann syndrome		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIAA0586 CL E G H	9786	19960	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	24
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIAA0586 CL E G H	9786	19960	ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	HP:0040283 - Occasional	24
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIAA0586 CL E G H	9786	19960	OMIM:616546	Short-Rib thoracic dysplasia 14 with polydactyly	.	24
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIAA0753 CL E G H	9851	29110	OMIM:619476	JOUBERT SYNDROME 38; JBTS38		4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIAA0753 CL E G H	9851	29110	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIF7 CL E G H	374654	30497	ORPHA:36	Acrocallosal syndrome		167
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KIF7 CL E G H	374654	30497	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	167
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	KRAS CL E G H	3845	6407	ORPHA:2612	Linear nevus sebaceus syndrome		196
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	L1CAM CL E G H	3897	6470	OMIM:304100	Corpus callosum, partial agenesis of, X-linked		134
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LAMA1 CL E G H	284217	6481	ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome		35
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LAMA1 CL E G H	284217	6481	OMIM:615960	Poretti-Boltshauser syndrome	.	35
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LAMB1 CL E G H	3912	6486	OMIM:615191	Lissencephaly 5		71
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	LAMB1 CL E G H	3912	6486	OMIM:615191	Lissencephaly 5		71
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LARGE1 CL E G H	9215	6511	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	136
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LARGE1 CL E G H	9215	6511	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		136
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LARGE1 CL E G H	9215	6511	OMIM:613154	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6		136
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LARGE1 CL E G H	9215	6511	ORPHA:899	Walker-Warburg syndrome		136
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LETM1 CL E G H	3954	6556	OMIM:620089			2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	LRRC32 CL E G H	2615	4161	OMIM:619074	CLEFT PALATE, PROLIFERATIVE RETINOPATHY, AND DEVELOPMENTAL DELAY; CPPRDD
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MAB21L1 CL E G H	4081	6757	OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	MACF1 CL E G H	23499	13664	OMIM:618325	Lissencephaly 9 with complex brainstem malformation		2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MACF1 CL E G H	23499	13664	OMIM:618325	Lissencephaly 9 with complex brainstem malformation		2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MAN2C1 CL E G H	4123	6827	OMIM:619775	CONGENITAL DISORDER OF DEGLYCOSYLATION 2; CDDG2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MAPKAPK5 CL E G H	8550	6889	OMIM:619869
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MBD5 CL E G H	55777	20444	OMIM:156200	Mental retardation, autosomal dominant 1		252
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MDH1 CL E G H	4190	6970	OMIM:618959	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88; DEE88
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MID1 CL E G H	4281	7095	ORPHA:2745	Opitz GBBB syndrome		57
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MID1 CL E G H	4281	7095	OMIM:300000	Opitz gbbb syndrome, type I		57
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	MINPP1 CL E G H	9562	7102	ORPHA:284339	Pontocerebellar hypoplasia type 7	HP:0040282 - Frequent	3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MKS1 CL E G H	54903	7121	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	127
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MKS1 CL E G H	54903	7121	ORPHA:220493	Joubert syndrome with ocular defect	HP:0040281 - Very frequent	127
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MKS1 CL E G H	54903	7121	ORPHA:564	Meckel syndrome		127
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MKS1 CL E G H	54903	7121	OMIM:249000	Meckel syndrome 1		127
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MPL CL E G H	4352	7217	OMIM:604498	Amegakaryocytic thrombocytopenia, congenital	.	97
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MRE11 CL E G H	4361	7230	ORPHA:251347	Ataxia-telangiectasia-like disorder	HP:0040282 - Frequent	532
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MTM1 CL E G H	4534	7448	OMIM:310400	Myopathy, centronuclear, X-linked		185
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MUSK CL E G H	4593	7525	ORPHA:994	Fetal akinesia deformation sequence		72
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	MYOD1 CL E G H	4654	7611	ORPHA:994	Fetal akinesia deformation sequence
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NCAPG2 CL E G H	54892	21904	OMIM:618460	Khan-Khan-Katsanis syndrome	.	2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NEK1 CL E G H	4750	7744	OMIM:263520	Short-Rib thoracic dysplasia 6 with or without polydactyly	HP:0040283 - Occasional	101
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NPHP1 CL E G H	4867	7905	OMIM:609583	Joubert syndrome 4	.	85
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NPHP1 CL E G H	4867	7905	ORPHA:220497	Joubert syndrome with renal defect	HP:0040281 - Very frequent	85
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NPHP3 CL E G H	27031	7907	OMIM:267010	MECKEL SYNDROME, TYPE 7; MKS7		157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NPHP3 CL E G H	27031	7907	ORPHA:3032	NPHP3-related Meckel-like syndrome		157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NPHP3 CL E G H	27031	7907	OMIM:208540	Renal-Hepatic-Pancreatic dysplasia		157
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NRAS CL E G H	4893	7989	ORPHA:2612	Linear nevus sebaceus syndrome		102
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NRAS CL E G H	4893	7989	OMIM:249400	Neurocutaneous melanosis, somatic		102
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NSD1 CL E G H	64324	14234	ORPHA:821	Sotos syndrome	HP:0040283 - Occasional	544
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NSRP1 CL E G H	84081	25305	OMIM:620001
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NUP37 CL E G H	79023	29929	OMIM:618179	Microcephaly 24, primary, autosomal recessive	.
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	NUP88 CL E G H	4927	8067	ORPHA:994	Fetal akinesia deformation sequence
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	OFD1 CL E G H	8481	2567	OMIM:300804	Joubert syndrome 10	.	201
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	OFD1 CL E G H	8481	2567	ORPHA:2750	Orofaciodigital syndrome type 1		201
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	OFD1 CL E G H	8481	2567	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	201
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	OPHN1 CL E G H	4983	8148	OMIM:300486	Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance		55
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PAFAH1B1 CL E G H	5048	8574	ORPHA:95232	Lissencephaly due to LIS1 mutation	HP:0040284 - Very rare	231
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PCGF2 CL E G H	7703	12929	OMIM:618371	Turnpenny-Fry syndrome	.
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PDE6D CL E G H	5147	8788	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PGAP1 CL E G H	80055	25712	OMIM:615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		20
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PHGDH CL E G H	26227	8923	OMIM:256520	Neu-Laxova syndrome		37
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PI4KA CL E G H	5297	8983	ORPHA:98889	Bilateral perisylvian polymicrogyria	HP:0040283 - Occasional	11
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PI4KA CL E G H	5297	8983	OMIM:616531	Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis		11
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PIBF1 CL E G H	10464	23352	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PIEZO2 CL E G H	63895	26270	OMIM:248700	Marden-Walker syndrome		77
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PIGN CL E G H	23556	8967	ORPHA:2059	Fryns syndrome		37
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PIGU CL E G H	128869	15791	OMIM:618590	NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES, SEIZURES, AND SCOLIOSIS; NEDBSS
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PLCH1 CL E G H	23007	29185	OMIM:619895
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PLG CL E G H	5340	9071	ORPHA:722	Hypoplasminogenemia		11
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PLG CL E G H	5340	9071	OMIM:217090	Plasminogen deficiency, type iligneous conjunctivitis, included		11
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	PMM2 CL E G H	5373	9115	OMIM:212065	Congenital disorder of glycosylation, type Ia	.	150
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PMM2 CL E G H	5373	9115	OMIM:212065	Congenital disorder of glycosylation, type Ia		150
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PMM2 CL E G H	5373	9115	ORPHA:79318	PMM2-CDG	HP:0040283 - Occasional	150
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POLR3A CL E G H	11128	30074	OMIM:264090	Wiedemann-Rautenstrauch syndrome		138
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	POMGNT1 CL E G H	55624	19139	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040283 - Occasional	180
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMGNT1 CL E G H	55624	19139	ORPHA:899	Walker-Warburg syndrome		180
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMGNT2 CL E G H	84892	25902	ORPHA:899	Walker-Warburg syndrome		33
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	POMK CL E G H	84197	26267	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040283 - Occasional	18
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMK CL E G H	84197	26267	ORPHA:899	Walker-Warburg syndrome		18
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	POMT1 CL E G H	10585	9202	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040283 - Occasional	213
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT1 CL E G H	10585	9202	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	213
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT1 CL E G H	10585	9202	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		213
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT1 CL E G H	10585	9202	OMIM:613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1		213
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT1 CL E G H	10585	9202	ORPHA:899	Walker-Warburg syndrome		213
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	POMT2 CL E G H	29954	19743	ORPHA:370959	Congenital muscular dystrophy with cerebellar involvement	HP:0040283 - Occasional	221
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT2 CL E G H	29954	19743	ORPHA:370968	Congenital muscular dystrophy with intellectual disability	HP:0040283 - Occasional	221
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT2 CL E G H	29954	19743	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		221
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	POMT2 CL E G H	29954	19743	ORPHA:899	Walker-Warburg syndrome		221
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PPFIBP1 CL E G H	8496	9249	OMIM:620024
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PPP1CB CL E G H	5500	9282	OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		9
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PPP1R21 CL E G H	129285	30595	OMIM:619383	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	PPP2R1A CL E G H	5518	9302	ORPHA:457284	Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome	HP:0040283 - Occasional	13
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PRDM13 CL E G H	59336	13998	OMIM:619909			2
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	PRDM13 CL E G H	59336	13998	OMIM:619909			2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PRKDC CL E G H	5591	9413	OMIM:615966	Immunodeficiency 26 with or without neurologic abnormalities	HP:0040283 - Occasional	42
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PSAT1 CL E G H	29968	19129	OMIM:610992	Phosphoserine aminotransferase deficiency	.	27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PSAT1 CL E G H	29968	19129	ORPHA:284417	Phosphoserine aminotransferase deficiency, infantile/juvenile form	HP:0040283 - Occasional	27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	PTEN CL E G H	5728	9588	ORPHA:101070	Bilateral frontoparietal polymicrogyria	HP:0040282 - Frequent	948
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	PTRH2 CL E G H	51651	24265	ORPHA:456312	Infantile multisystem neurologic-endocrine-pancreatic disease	HP:0040282 - Frequent	6
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAB11B CL E G H	9230	9761	OMIM:617807	Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter	.
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAB18 CL E G H	22931	14244	ORPHA:2510	Micro syndrome	HP:0040283 - Occasional	85
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAB3GAP1 CL E G H	22930	17063	ORPHA:2510	Micro syndrome	HP:0040283 - Occasional	90
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAB3GAP1 CL E G H	22930	17063	OMIM:600118	Warburg micro syndrome 1		90
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAB3GAP2 CL E G H	25782	17168	ORPHA:2510	Micro syndrome	HP:0040283 - Occasional	135
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAC1 CL E G H	5879	9801	OMIM:617751	Mental retardation, autosomal dominant 48		3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RAPSN CL E G H	5913	9863	ORPHA:994	Fetal akinesia deformation sequence		73
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RARS2 CL E G H	57038	21406	OMIM:611523	Pontocerebellar hypoplasia, type 6		93
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RBM10 CL E G H	8241	9896	OMIM:311900	Tarp syndrome	.	16
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RBM8A CL E G H	9939	9905	OMIM:274000	Thrombocytopenia-absent radius syndrome		10
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RERE CL E G H	473	9965	OMIM:616975	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart		16
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RERE CL E G H	473	9965	ORPHA:494344	RERE-related neurodevelopmental syndrome	HP:0040283 - Occasional	16
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RNF113A CL E G H	7737	12974	OMIM:300953	Trichothiodystrophy 5, nonphotosensitive		3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RNU4ATAC CL E G H	100151683	34016	OMIM:210710	Microcephalic osteodysplastic primordial dwarfism, type I		15
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RPE65 CL E G H	6121	10294	OMIM:204100	Leber congenital amaurosis, type II	.	129
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RPGRIP1 CL E G H	57096	13436	ORPHA:564	Meckel syndrome		109
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RPGRIP1L CL E G H	23322	29168	ORPHA:1454	Joubert syndrome with hepatic defect	HP:0040281 - Very frequent	167
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RPGRIP1L CL E G H	23322	29168	ORPHA:220497	Joubert syndrome with renal defect	HP:0040281 - Very frequent	167
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RPGRIP1L CL E G H	23322	29168	ORPHA:564	Meckel syndrome		167
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	RTTN CL E G H	25914	18654	ORPHA:468631	Microcephalic cortical malformations-short stature due to RTTN deficiency	HP:0040283 - Occasional	113
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	RXYLT1 CL E G H	10329	13530	ORPHA:899	Walker-Warburg syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SACS CL E G H	26278	10519	ORPHA:98	Autosomal recessive spastic ataxia of Charlevoix-Saguenay	HP:0040282 - Frequent	309
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SEMA3E CL E G H	9723	10727	ORPHA:138	CHARGE syndrome		16
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SEMA6B CL E G H	10501	10739	OMIM:618876	EPILEPSY, PROGRESSIVE MYOCLONIC, 11; EPM11
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SEPSECS CL E G H	51091	30605	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	66
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SETD2 CL E G H	29072	18420	ORPHA:821	Sotos syndrome	HP:0040283 - Occasional	60
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SLC18A3 CL E G H	6572	10936	ORPHA:994	Fetal akinesia deformation sequence		2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SLC25A19 CL E G H	60386	14409	ORPHA:99742	Amish lethal microcephaly	HP:0040281 - Very frequent	36
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SLC25A24 CL E G H	29957	20662	OMIM:612289	Fontaine progeroid syndrome	.
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SLC35A2 CL E G H	7355	11022	ORPHA:356961	SLC35A2-CDG		27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCA4 CL E G H	6597	11100	ORPHA:1465	Coffin-Siris syndrome		617
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCA4 CL E G H	6597	11100	OMIM:614609	Coffin-Siris syndrome 4		617
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCB1 CL E G H	6598	11103	ORPHA:1465	Coffin-Siris syndrome		87
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCC2 CL E G H	6601	11105	ORPHA:1465	Coffin-Siris syndrome		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCD1 CL E G H	6602	11106	ORPHA:1465	Coffin-Siris syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCE1 CL E G H	6605	11109	ORPHA:1465	Coffin-Siris syndrome		47
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMARCE1 CL E G H	6605	11109	OMIM:616938	Coffin-Siris syndrome 5		47
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SMG9 CL E G H	56006	25763	OMIM:616920	Heart and brain malformation syndrome		2
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	SON CL E G H	6651	11183	ORPHA:500150	Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome	HP:0040283 - Occasional	12
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SOX11 CL E G H	6664	11191	ORPHA:1465	Coffin-Siris syndrome		14
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SOX4 CL E G H	6659	11200	ORPHA:1465	Coffin-Siris syndrome
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SRD5A3 CL E G H	79644	25812	OMIM:612379	Congenital disorder of glycosylation, type IQ	.	80
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SRPX2 CL E G H	27286	30668	ORPHA:98889	Bilateral perisylvian polymicrogyria	HP:0040283 - Occasional	50
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SUFU CL E G H	51684	16466	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	124
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	SYT2 CL E G H	127833	11510	OMIM:619461	MYASTHENIC SYNDROME, CONGENITAL, 7B, PRESYNAPTIC, AUTOSOMAL RECESSIVE; CMS7B		4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TAF1 CL E G H	6872	11535	OMIM:300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33; MRXS33		21
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TBC1D20 CL E G H	128637	16133	ORPHA:2510	Micro syndrome	HP:0040283 - Occasional	15
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TBC1D24 CL E G H	57465	29203	OMIM:220500	Doors syndrome		271
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TBC1D24 CL E G H	57465	29203	ORPHA:79500	DOORS syndrome		271
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TBCK CL E G H	93627	28261	OMIM:616900	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3		13
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN1 CL E G H	79600	26113	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN1 CL E G H	79600	26113	OMIM:614173	Joubert syndrome 13		45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN1 CL E G H	79600	26113	ORPHA:564	Meckel syndrome		45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN2 CL E G H	79867	25774	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	76
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN2 CL E G H	79867	25774	ORPHA:564	Meckel syndrome		76
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN3 CL E G H	26123	24519	ORPHA:564	Meckel syndrome		31
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TCTN3 CL E G H	26123	24519	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	31
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	THG1L CL E G H	54974	26053	OMIM:618800	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 28; SCAR28
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	THOC2 CL E G H	57187	19073	OMIM:300957	Mental retardation, X-linked 12/35		5
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMCO1 CL E G H	54499	18188	ORPHA:1394	Cerebrofaciothoracic dysplasia	HP:0040282 - Frequent	6
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM107 CL E G H	84314	28128	ORPHA:564	Meckel syndrome		4
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM138 CL E G H	51524	26944	OMIM:614465	JOUBERT SYNDROME 16; JBTS16		39
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM138 CL E G H	51524	26944	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	39
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM216 CL E G H	51259	25018	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM216 CL E G H	51259	25018	ORPHA:564	Meckel syndrome		45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM216 CL E G H	51259	25018	OMIM:603194	Meckel syndrome, type 2		45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM216 CL E G H	51259	25018	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	45
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM218 CL E G H	219854	27344	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM218 CL E G H	219854	27344	OMIM:619562	JOUBERT SYNDROME 39; JBTS39
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM231 CL E G H	79583	37234	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	33
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM231 CL E G H	79583	37234	ORPHA:564	Meckel syndrome		33
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM231 CL E G H	79583	37234	ORPHA:2752	Orofaciodigital syndrome type 3	HP:0040282 - Frequent	33
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM237 CL E G H	65062	14432	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	82
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM237 CL E G H	65062	14432	OMIM:614424	Joubert syndrome 14		82
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM237 CL E G H	65062	14432	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	82
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM237 CL E G H	65062	14432	ORPHA:220497	Joubert syndrome with renal defect	HP:0040281 - Very frequent	82
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM237 CL E G H	65062	14432	ORPHA:564	Meckel syndrome		82
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM67 CL E G H	91147	28396	OMIM:216360	Coach syndrome 1	.	166
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM67 CL E G H	91147	28396	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent	166
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM67 CL E G H	91147	28396	OMIM:610688	Joubert syndrome 6	.	166
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM67 CL E G H	91147	28396	ORPHA:1454	Joubert syndrome with hepatic defect	HP:0040281 - Very frequent	166
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM67 CL E G H	91147	28396	ORPHA:564	Meckel syndrome		166
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TMEM67 CL E G H	91147	28396	OMIM:607361	Meckel syndrome 3		166
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	TOE1 CL E G H	114034	15954	ORPHA:284339	Pontocerebellar hypoplasia type 7	HP:0040282 - Frequent	6
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TOGARAM1 CL E G H	23116	19959	ORPHA:475	Joubert syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TOGARAM1 CL E G H	23116	19959	OMIM:619185	JOUBERT SYNDROME 37; JBTS37
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TOPORS CL E G H	10210	21653	ORPHA:2754	Orofaciodigital syndrome type 6	HP:0040283 - Occasional	61
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TRAPPC9 CL E G H	83696	30832	OMIM:613192	Mental retardation, autosomal recessive 13		158
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TRIP13 CL E G H	9319	12307	ORPHA:1052	Mosaic variegated aneuploidy syndrome		2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TRRAP CL E G H	8295	12347	OMIM:618454	Developmental delay with or without dysmorphic facies and autism	.	2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TSEN15 CL E G H	116461	16791	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TSEN2 CL E G H	80746	28422	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	84
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TSEN2 CL E G H	80746	28422	OMIM:612389	Pontocerebellar hypoplasia, type 2B		84
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TSEN34 CL E G H	79042	15506	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	57
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	TSEN34 CL E G H	79042	15506	OMIM:612390	PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		57
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TSEN34 CL E G H	79042	15506	OMIM:612390	PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		57
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TSEN54 CL E G H	283989	27561	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040281 - Very frequent	102
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	TSEN54 CL E G H	283989	27561	ORPHA:166063	Pontocerebellar hypoplasia type 4	HP:0040282 - Frequent	102
HP:0001321	HP:0006955	Olivopontocerebellar hypoplasia	1	TSEN54 CL E G H	283989	27561	OMIM:610204	Pontocerebellar hypoplasia, type 5	.	102
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBA1A CL E G H	7846	20766	ORPHA:994	Fetal akinesia deformation sequence		106
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBA1A CL E G H	7846	20766	OMIM:611603	Lissencephaly 3	.	106
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBA1A CL E G H	7846	20766	ORPHA:171680	Lissencephaly due to TUBA1A mutation		106
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBA1A CL E G H	7846	20766	ORPHA:467166	Tubulinopathy-associated dysgyria		106
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBB CL E G H	203068	20778	OMIM:615771	Cortical dysplasia, complex, with other brain malformations 6		14
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBB CL E G H	203068	20778	OMIM:156610	Skin creases, congenital symmetric circumferential, 1		14
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBB2B CL E G H	347733	30829	ORPHA:467166	Tubulinopathy-associated dysgyria		39
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBB3 CL E G H	10381	20772	ORPHA:300570	Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	HP:0040283 - Occasional	64
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TUBB3 CL E G H	10381	20772	ORPHA:467166	Tubulinopathy-associated dysgyria		64
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	TXNDC15 CL E G H	79770	20652	ORPHA:564	Meckel syndrome		2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	USP9X CL E G H	8239	12632	OMIM:300968	Mental retardation, X-linked 99, syndromic, female-restricted		27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	USP9X CL E G H	8239	12632	ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability	HP:0040283 - Occasional	27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	VPS35L CL E G H	57020	24641	OMIM:619135	RITSCHER-SCHINZEL SYNDROME 3; RTSC3
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	VPS4A CL E G H	27183	13488	OMIM:619273	CIMDAG SYNDROME; CIMDAG		1
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	VPS51 CL E G H	738	1172	OMIM:618606	PONTOCEREBELLAR HYPOPLASIA, TYPE 13; PCH13
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WARS2 CL E G H	10352	12730	ORPHA:572798	WARS2-related combined oxidative phosphorylation defect	HP:0040283 - Occasional	2
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WASHC5 CL E G H	9897	28984	ORPHA:7	3C syndrome		83
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WASHC5 CL E G H	9897	28984	OMIM:220210	Ritscher-Schinzel syndrome 1		83
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WDR35 CL E G H	57539	29250	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type		136
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WDR73 CL E G H	84942	25928	OMIM:251300	Galloway-mowat syndrome 1		14
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WDR81 CL E G H	124997	26600	OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies		27
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	WLS CL E G H	79971	30238	OMIM:619648	ZAKI SYNDROME; ZKS
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ZEB2 CL E G H	9839	14881	ORPHA:261552	Mowat-Wilson syndrome due to a ZEB2 point mutation	HP:0040284 - Very rare	362
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ZEB2 CL E G H	9839	14881	ORPHA:261537	Mowat-Wilson syndrome due to monosomy 2q22	HP:0040284 - Very rare	362
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ZIC1 CL E G H	7545	12872	OMIM:616602	Craniosynostosis 6		5
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ZIC1 CL E G H	7545	12872	OMIM:618736	STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS		5
HP:0001321	HP:0100307	Cerebellar hemisphere hypoplasia	1	ZNF335 CL E G H	63925	15807	OMIM:615095	Microcephaly 10, primary, autosomal recessive		60
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ZNF423 CL E G H	23090	16762	ORPHA:2318	Joubert syndrome with oculorenal defect	HP:0040281 - Very frequent	49
HP:0001321	HP:0001320	Cerebellar vermis hypoplasia	1	ZNF423 CL E G H	23090	16762	OMIM:614844	Nephronophthisis 14	.	49
HP:0001321	HP:0001305	Dandy-Walker malformation	2	AFF3 CL E G H	3899	6473	OMIM:619297	KINSSHIP SYNDROME; KINS		1
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ALG3 CL E G H	10195	23056	ORPHA:79321	ALG3-CDG	HP:0040284 - Very rare	37
HP:0001321	HP:0001305	Dandy-Walker malformation	2	AP1S2 CL E G H	8905	560	OMIM:304340	Pettigrew syndrome	HP:0040283 - Occasional	13
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ARID1A CL E G H	8289	11110	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	88
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ARID1A CL E G H	8289	11110	OMIM:614607	Coffin-Siris syndrome 2		88
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ARID1B CL E G H	57492	18040	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	219
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ARID1B CL E G H	57492	18040	OMIM:135900	Coffin-Siris syndrome 1	.	219
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ARID2 CL E G H	196528	18037	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	25
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ARMC9 CL E G H	80210	20730	OMIM:617622	JOUBERT SYNDROME 30; JBTS30
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ASXL1 CL E G H	171023	18318	ORPHA:97297	Bohring-Opitz syndrome	HP:0040283 - Occasional	145
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ASXL1 CL E G H	171023	18318	OMIM:605039	Bohring-Opitz syndrome	.	145
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	ASXL3 CL E G H	80816	29357	OMIM:615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		49
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ATP6V0A2 CL E G H	23545	18481	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	HP:0040282 - Frequent	140
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ATP6V0A2 CL E G H	23545	18481	OMIM:219200	Cutis laxa, autosomal recessive, type IIA	.	140
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ATP6V0A2 CL E G H	23545	18481	ORPHA:2834	Wrinkly skin syndrome	HP:0040282 - Frequent	140
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ATP6V1A CL E G H	523	851	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	HP:0040282 - Frequent	3
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ATP6V1B2 CL E G H	526	854	ORPHA:79500	DOORS syndrome	HP:0040284 - Very rare	5
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ATP6V1E1 CL E G H	529	857	ORPHA:357074	Autosomal recessive cutis laxa type 2, classic type	HP:0040282 - Frequent	2
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B3GALNT2 CL E G H	148789	28596	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	43
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B4GALT1 CL E G H	2683	924	ORPHA:79332	B4GALT1-CDG	HP:0040281 - Very frequent	85
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B4GALT1 CL E G H	2683	924	OMIM:607091	Congenital disorder of glycosylation, type IID	.	85
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B4GAT1 CL E G H	11041	15685	OMIM:615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13	.	17
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B4GAT1 CL E G H	11041	15685	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	17
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B9D1 CL E G H	27077	24123	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	28
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B9D2 CL E G H	80776	28636	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	34
HP:0001321	HP:0001305	Dandy-Walker malformation	2	B9D2 CL E G H	80776	28636	OMIM:614175	Meckel syndrome, type 10		34
HP:0001321	HP:0001305	Dandy-Walker malformation	2	BCOR CL E G H	54880	20893	OMIM:300166	Microphthalmia, syndromic 2		101
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	BMP4 CL E G H	652	1071	ORPHA:139471	Microphthalmia with brain and digit anomalies	HP:0040283 - Occasional	38
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	BMP4 CL E G H	652	1071	OMIM:607932	Microphthalmia, syndromic 6		38
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	BRF1 CL E G H	2972	11551	ORPHA:444072	Cerebellar-facial-dental syndrome	HP:0040283 - Occasional	7
HP:0001321	HP:0001305	Dandy-Walker malformation	2	BUB1 CL E G H	699	1148	ORPHA:1052	Mosaic variegated aneuploidy syndrome	HP:0040281 - Very frequent	5
HP:0001321	HP:0001305	Dandy-Walker malformation	2	BUB1B CL E G H	701	1149	ORPHA:1052	Mosaic variegated aneuploidy syndrome	HP:0040281 - Very frequent	76
HP:0001321	HP:0001305	Dandy-Walker malformation	2	BUB1B CL E G H	701	1149	OMIM:257300	Mosaic variegated aneuploidy syndrome 1	.	76
HP:0001321	HP:0001305	Dandy-Walker malformation	2	BUB3 CL E G H	9184	1151	ORPHA:1052	Mosaic variegated aneuploidy syndrome	HP:0040281 - Very frequent
HP:0001321	HP:0001305	Dandy-Walker malformation	2	C2CD3 CL E G H	26005	24564	ORPHA:434179	Orofaciodigital syndrome type 14	HP:0040282 - Frequent	27
HP:0001321	HP:0001305	Dandy-Walker malformation	2	C2CD3 CL E G H	26005	24564	OMIM:615948	Orofaciodigital syndrome XIV	.	27
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CC2D2A CL E G H	57545	29253	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	247
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CCDC22 CL E G H	28952	28909	ORPHA:7	3C syndrome	HP:0040281 - Very frequent	33
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CCDC22 CL E G H	28952	28909	OMIM:300963	Ritscher-Schinzel syndrome 2	.	33
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CDC42 CL E G H	998	1736	ORPHA:487796	Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome	HP:0040283 - Occasional	6
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CDKN1C CL E G H	1028	1786	OMIM:130650	Beckwith-Wiedemann syndrome	HP:0040283 - Occasional	114
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CEP120 CL E G H	153241	26690	OMIM:616300	Short-Rib thoracic dysplasia 13 with or without polydactyly	.	7
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CEP290 CL E G H	80184	29021	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	342
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CEP290 CL E G H	80184	29021	OMIM:611134	Meckel syndrome, type 4		342
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CEP57 CL E G H	9702	30794	ORPHA:1052	Mosaic variegated aneuploidy syndrome	HP:0040281 - Very frequent	17
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CHD7 CL E G H	55636	20626	ORPHA:138	CHARGE syndrome	HP:0040283 - Occasional	515
HP:0001321	HP:0001305	Dandy-Walker malformation	2	COL4A1 CL E G H	1282	2202	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	193
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CPT2 CL E G H	1376	2330	ORPHA:228305	Carnitine palmitoyl transferase II deficiency, severe infantile form	HP:0040283 - Occasional	101
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CRPPA CL E G H	729920	37276	OMIM:614643	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7	.
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CRPPA CL E G H	729920	37276	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CSF1R CL E G H	1436	2433	OMIM:618476	Brain abnormalities, neurodegeneration, and dysosteosclerosis		149
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CSPP1 CL E G H	79848	26193	ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	HP:0040283 - Occasional	57
HP:0001321	HP:0001305	Dandy-Walker malformation	2	CSPP1 CL E G H	79848	26193	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	57
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DAG1 CL E G H	1605	2666	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	108
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DENND5A CL E G H	23258	19344	OMIM:617281	Epileptic encephalopathy, early infantile, 49	HP:0040284 - Very rare	6
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DHCR7 CL E G H	1717	2860	OMIM:270400	Smith-Lemli-Opitz syndrome		159
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DOK7 CL E G H	285489	26594	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional	91
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DPF2 CL E G H	5977	9964	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DPH1 CL E G H	1801	3003	ORPHA:459061	Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome	HP:0040282 - Frequent	3
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DPH1 CL E G H	1801	3003	OMIM:616901	Developmental delay with short stature, dysmorphic features, and sparse hair	HP:0040283 - Occasional	3
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DPYSL5 CL E G H	56896	20637	OMIM:619435	RITSCHER-SCHINZEL SYNDROME 4; RTSC4
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DYNC2H1 CL E G H	79659	2962	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional	304
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DYNC2I1 CL E G H	55112	21862	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	DYNC2I2 CL E G H	89891	28296	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	EBP CL E G H	10682	3133	OMIM:302960	Chondrodysplasia punctata 2, X-linked dominant	.	51
HP:0001321	HP:0001305	Dandy-Walker malformation	2	EBP CL E G H	10682	3133	OMIM:300960	Mend syndrome	.	51
HP:0001321	HP:0001305	Dandy-Walker malformation	2	EBP CL E G H	10682	3133	ORPHA:401973	MEND syndrome	HP:0040282 - Frequent	51
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ESCO2 CL E G H	157570	27230	ORPHA:2319	Juberg-Hayward syndrome	HP:0040283 - Occasional	92
HP:0001321	HP:0001305	Dandy-Walker malformation	2	EVC CL E G H	2121	3497	OMIM:225500	Ellis-Van creveld syndrome	.	209
HP:0001321	HP:0001305	Dandy-Walker malformation	2	EVC2 CL E G H	132884	19747	OMIM:225500	Ellis-Van creveld syndrome	.	137
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FAR1 CL E G H	84188	26222	ORPHA:438178	Fatty acyl-CoA reductase 1 deficiency	HP:0040283 - Occasional	7
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FAR1 CL E G H	84188	26222	OMIM:616154	PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER; PFCRD		7
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FGFR1 CL E G H	2260	3688	OMIM:613001	Encephalocraniocutaneous lipomatosis	.	172
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FKRP CL E G H	79147	17997	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		157
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FKRP CL E G H	79147	17997	OMIM:613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5	.	157
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FKRP CL E G H	79147	17997	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	157
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FKTN CL E G H	2218	3622	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		184
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FKTN CL E G H	2218	3622	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	184
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FLVCR2 CL E G H	55640	20105	OMIM:225790	Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome	.	47
HP:0001321	HP:0001305	Dandy-Walker malformation	2	FTO CL E G H	79068	24678	OMIM:612938	Growth retardation, developmental delay, coarse facies, and earlydeath	.	70
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	GEMIN4 CL E G H	50628	15717	OMIM:617913	Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities		1
HP:0001321	HP:0001305	Dandy-Walker malformation	2	GJB2 CL E G H	2706	4284	ORPHA:477	KID syndrome		199
HP:0001321	HP:0001305	Dandy-Walker malformation	2	GJB6 CL E G H	10804	4288	ORPHA:477	KID syndrome		56
HP:0001321	HP:0001305	Dandy-Walker malformation	2	GLI3 CL E G H	2737	4319	ORPHA:36	Acrocallosal syndrome	HP:0040282 - Frequent	270
HP:0001321	HP:0001305	Dandy-Walker malformation	2	GPC3 CL E G H	2719	4451	ORPHA:373	Simpson-Golabi-Behmel syndrome	HP:0040283 - Occasional	73
HP:0001321	HP:0001305	Dandy-Walker malformation	2	GPC4 CL E G H	2239	4452	ORPHA:373	Simpson-Golabi-Behmel syndrome	HP:0040283 - Occasional
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	GRM1 CL E G H	2911	4593	OMIM:614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13; SCAR13		8
HP:0001321	HP:0001305	Dandy-Walker malformation	2	GTPBP2 CL E G H	54676	4670	OMIM:617988	Jaberi-Elahi syndrome
HP:0001321	HP:0001305	Dandy-Walker malformation	2	H19-ICR CL E G H	105259599		OMIM:130650	Beckwith-Wiedemann syndrome	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	HRAS CL E G H	3265	5173	ORPHA:2612	Linear nevus sebaceus syndrome	HP:0040283 - Occasional	113
HP:0001321	HP:0001305	Dandy-Walker malformation	2	HYLS1 CL E G H	219844	26558	OMIM:236680	Hydrolethalus syndrome 1	.	31
HP:0001321	HP:0001305	Dandy-Walker malformation	2	IFT80 CL E G H	57560	29262	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional	65
HP:0001321	HP:0001305	Dandy-Walker malformation	2	IGF2 CL E G H	3481	5466	OMIM:130650	Beckwith-Wiedemann syndrome	HP:0040283 - Occasional	9
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	INTS1 CL E G H	26173	24555	OMIM:618571	NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES; NDCAGF
HP:0001321	HP:0001305	Dandy-Walker malformation	2	KCNQ1 CL E G H	3784	6294	OMIM:130650	Beckwith-Wiedemann syndrome	HP:0040283 - Occasional	730
HP:0001321	HP:0001305	Dandy-Walker malformation	2	KCNQ1OT1 CL E G H	10984	6295	OMIM:130650	Beckwith-Wiedemann syndrome	HP:0040283 - Occasional	1
HP:0001321	HP:0001305	Dandy-Walker malformation	2	KIAA0586 CL E G H	9786	19960	ORPHA:397715	Joubert syndrome with Jeune asphyxiating thoracic dystrophy	HP:0040283 - Occasional	24
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	KIAA0753 CL E G H	9851	29110	OMIM:619476	JOUBERT SYNDROME 38; JBTS38		4
HP:0001321	HP:0001305	Dandy-Walker malformation	2	KIF7 CL E G H	374654	30497	ORPHA:36	Acrocallosal syndrome	HP:0040282 - Frequent	167
HP:0001321	HP:0001305	Dandy-Walker malformation	2	KRAS CL E G H	3845	6407	ORPHA:2612	Linear nevus sebaceus syndrome	HP:0040283 - Occasional	196
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	L1CAM CL E G H	3897	6470	OMIM:304100	Corpus callosum, partial agenesis of, X-linked	.	134
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	LAMA1 CL E G H	284217	6481	ORPHA:370022	Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome	HP:0040282 - Frequent	35
HP:0001321	HP:0001305	Dandy-Walker malformation	2	LARGE1 CL E G H	9215	6511	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		136
HP:0001321	HP:0001305	Dandy-Walker malformation	2	LARGE1 CL E G H	9215	6511	OMIM:613154	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6	HP:0040282 - Frequent	136
HP:0001321	HP:0001305	Dandy-Walker malformation	2	LARGE1 CL E G H	9215	6511	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	136
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MAB21L1 CL E G H	4081	6757	OMIM:618479	Cerebellar, ocular, craniofacial, and genital syndrome	.
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	MDH1 CL E G H	4190	6970	OMIM:618959	DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88; DEE88
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MID1 CL E G H	4281	7095	ORPHA:2745	Opitz GBBB syndrome	HP:0040283 - Occasional	57
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MKS1 CL E G H	54903	7121	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	127
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MKS1 CL E G H	54903	7121	OMIM:249000	Meckel syndrome 1	.	127
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MTM1 CL E G H	4534	7448	OMIM:310400	Myopathy, centronuclear, X-linked		185
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MUSK CL E G H	4593	7525	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional	72
HP:0001321	HP:0001305	Dandy-Walker malformation	2	MYOD1 CL E G H	4654	7611	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	NPHP3 CL E G H	27031	7907	OMIM:267010	MECKEL SYNDROME, TYPE 7; MKS7		157
HP:0001321	HP:0001305	Dandy-Walker malformation	2	NPHP3 CL E G H	27031	7907	ORPHA:3032	NPHP3-related Meckel-like syndrome	HP:0040281 - Very frequent	157
HP:0001321	HP:0001305	Dandy-Walker malformation	2	NPHP3 CL E G H	27031	7907	OMIM:208540	Renal-Hepatic-Pancreatic dysplasia	HP:0040283 - Occasional	157
HP:0001321	HP:0001305	Dandy-Walker malformation	2	NRAS CL E G H	4893	7989	ORPHA:2612	Linear nevus sebaceus syndrome	HP:0040283 - Occasional	102
HP:0001321	HP:0001305	Dandy-Walker malformation	2	NRAS CL E G H	4893	7989	OMIM:249400	Neurocutaneous melanosis, somatic	HP:0040283 - Occasional	102
HP:0001321	HP:0001305	Dandy-Walker malformation	2	NUP88 CL E G H	4927	8067	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	OFD1 CL E G H	8481	2567	ORPHA:2750	Orofaciodigital syndrome type 1	HP:0040283 - Occasional	201
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PHGDH CL E G H	26227	8923	OMIM:256520	Neu-Laxova syndrome	.	37
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	PIEZO2 CL E G H	63895	26270	OMIM:248700	Marden-Walker syndrome	.	77
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PIEZO2 CL E G H	63895	26270	OMIM:248700	Marden-Walker syndrome	.	77
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PIGN CL E G H	23556	8967	ORPHA:2059	Fryns syndrome	HP:0040283 - Occasional	37
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PLCH1 CL E G H	23007	29185	OMIM:619895
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PLG CL E G H	5340	9071	ORPHA:722	Hypoplasminogenemia	HP:0040283 - Occasional	11
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PLG CL E G H	5340	9071	OMIM:217090	Plasminogen deficiency, type iligneous conjunctivitis, included	.	11
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PMM2 CL E G H	5373	9115	ORPHA:79318	PMM2-CDG	HP:0040284 - Very rare	150
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POLR3A CL E G H	11128	30074	OMIM:264090	Wiedemann-Rautenstrauch syndrome	.	138
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMGNT1 CL E G H	55624	19139	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	180
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMGNT2 CL E G H	84892	25902	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	33
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMK CL E G H	84197	26267	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	18
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMT1 CL E G H	10585	9202	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		213
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMT1 CL E G H	10585	9202	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	213
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMT2 CL E G H	29954	19743	OMIM:236670	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1		221
HP:0001321	HP:0001305	Dandy-Walker malformation	2	POMT2 CL E G H	29954	19743	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent	221
HP:0001321	HP:0001305	Dandy-Walker malformation	2	PPP1CB CL E G H	5500	9282	OMIM:617506	Noonan syndrome-like disorder with loose anagen hair 2		9
HP:0001321	HP:0001305	Dandy-Walker malformation	2	RAPSN CL E G H	5913	9863	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional	73
HP:0001321	HP:0001305	Dandy-Walker malformation	2	RNF113A CL E G H	7737	12974	OMIM:300953	Trichothiodystrophy 5, nonphotosensitive	.	3
HP:0001321	HP:0001305	Dandy-Walker malformation	2	RPGRIP1 CL E G H	57096	13436	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	109
HP:0001321	HP:0001305	Dandy-Walker malformation	2	RPGRIP1L CL E G H	23322	29168	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	167
HP:0001321	HP:0001305	Dandy-Walker malformation	2	RXYLT1 CL E G H	10329	13530	ORPHA:899	Walker-Warburg syndrome	HP:0040282 - Frequent
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SEMA3E CL E G H	9723	10727	ORPHA:138	CHARGE syndrome	HP:0040283 - Occasional	16
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SLC18A3 CL E G H	6572	10936	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional	2
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SLC35A2 CL E G H	7355	11022	ORPHA:356961	SLC35A2-CDG	HP:0040284 - Very rare	27
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCA4 CL E G H	6597	11100	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	617
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCA4 CL E G H	6597	11100	OMIM:614609	Coffin-Siris syndrome 4		617
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCB1 CL E G H	6598	11103	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	87
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCC2 CL E G H	6601	11105	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	1
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCD1 CL E G H	6602	11106	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCE1 CL E G H	6605	11109	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	47
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMARCE1 CL E G H	6605	11109	OMIM:616938	Coffin-Siris syndrome 5	.	47
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SMG9 CL E G H	56006	25763	OMIM:616920	Heart and brain malformation syndrome		2
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SOX11 CL E G H	6664	11191	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional	14
HP:0001321	HP:0001305	Dandy-Walker malformation	2	SOX4 CL E G H	6659	11200	ORPHA:1465	Coffin-Siris syndrome	HP:0040283 - Occasional
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TBC1D24 CL E G H	57465	29203	OMIM:220500	Doors syndrome	HP:0040283 - Occasional	271
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TBC1D24 CL E G H	57465	29203	ORPHA:79500	DOORS syndrome	HP:0040284 - Very rare	271
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TCTN1 CL E G H	79600	26113	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	45
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TCTN2 CL E G H	79867	25774	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	76
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TCTN3 CL E G H	26123	24519	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	31
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM107 CL E G H	84314	28128	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	4
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM138 CL E G H	51524	26944	OMIM:614465	JOUBERT SYNDROME 16; JBTS16		39
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM216 CL E G H	51259	25018	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	45
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM216 CL E G H	51259	25018	OMIM:603194	Meckel syndrome, type 2	HP:0040283 - Occasional	45
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM231 CL E G H	79583	37234	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	33
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM231 CL E G H	79583	37234	ORPHA:2752	Orofaciodigital syndrome type 3	HP:0040282 - Frequent	33
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM237 CL E G H	65062	14432	OMIM:614424	Joubert syndrome 14	.	82
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM237 CL E G H	65062	14432	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	82
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM67 CL E G H	91147	28396	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	166
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TMEM67 CL E G H	91147	28396	OMIM:607361	Meckel syndrome 3		166
HP:0001321	HP:0007068	Inferior cerebellar vermis hypoplasia	2	TRAPPC9 CL E G H	83696	30832	OMIM:613192	Mental retardation, autosomal recessive 13		158
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TRIP13 CL E G H	9319	12307	ORPHA:1052	Mosaic variegated aneuploidy syndrome	HP:0040281 - Very frequent	2
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TUBA1A CL E G H	7846	20766	ORPHA:994	Fetal akinesia deformation sequence	HP:0040283 - Occasional	106
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TUBB CL E G H	203068	20778	OMIM:156610	Skin creases, congenital symmetric circumferential, 1	HP:0040283 - Occasional	14
HP:0001321	HP:0001305	Dandy-Walker malformation	2	TXNDC15 CL E G H	79770	20652	ORPHA:564	Meckel syndrome	HP:0040283 - Occasional	2
HP:0001321	HP:0001305	Dandy-Walker malformation	2	USP9X CL E G H	8239	12632	OMIM:300968	Mental retardation, X-linked 99, syndromic, female-restricted		27
HP:0001321	HP:0001305	Dandy-Walker malformation	2	USP9X CL E G H	8239	12632	ORPHA:480880	X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability	HP:0040282 - Frequent	27
HP:0001321	HP:0001305	Dandy-Walker malformation	2	VPS51 CL E G H	738	1172	OMIM:618606	PONTOCEREBELLAR HYPOPLASIA, TYPE 13; PCH13
HP:0001321	HP:0001305	Dandy-Walker malformation	2	WASHC5 CL E G H	9897	28984	ORPHA:7	3C syndrome	HP:0040281 - Very frequent	83
HP:0001321	HP:0001305	Dandy-Walker malformation	2	WASHC5 CL E G H	9897	28984	OMIM:220210	Ritscher-Schinzel syndrome 1	.	83
HP:0001321	HP:0001305	Dandy-Walker malformation	2	WDR35 CL E G H	57539	29250	ORPHA:93271	Short rib-polydactyly syndrome, Verma-Naumoff type	HP:0040283 - Occasional	136
HP:0001321	HP:0001305	Dandy-Walker malformation	2	WDR73 CL E G H	84942	25928	OMIM:251300	Galloway-mowat syndrome 1	HP:0040283 - Occasional	14
HP:0001321	HP:0001305	Dandy-Walker malformation	2	WDR81 CL E G H	124997	26600	OMIM:617967	Hydrocephalus, congenital, 3, with brain anomalies	.	27
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ZIC1 CL E G H	7545	12872	OMIM:616602	Craniosynostosis 6	HP:0040283 - Occasional	5
HP:0001321	HP:0001305	Dandy-Walker malformation	2	ZIC1 CL E G H	7545	12872	OMIM:618736	STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS		5

Genes (416) :ABAT ACD ADGRG1 AFF3 AFG3L2 AHCY AHI1 ALG12 ALG3 ALG6 ALX4 AP1S2 APC2 ARHGEF2 ARID1A ARID1B ARID2 ARL13B ARL3 ARMC9 ARSI ASNS ASPM ASXL1 ASXL3 ATAD3A ATCAY ATG5 ATG7 ATN1 ATP2B3 ATP5F1A ATP6V0A1 ATP6V0A2 ATP6V1A ATP6V1B2 ATP6V1E1 ATR ATXN2 B3GALNT2 B4GALT1 B4GAT1 B9D1 B9D2 BCOR BICD2 BLTP1 BMP4 BRF1 BUB1 BUB1B BUB3 C2CD3 CACNA1G CAMTA1 CARS2 CASK CBY1 CC2D2A CCDC22 CCDC32 CDC40 CDC42 CDC42BPB CDK5 CDKN1C CENPE CENPF CEP104 CEP120 CEP164 CEP290 CEP41 CEP55 CEP57 CHD7 CHMP1A CIT CLCN3 COASY COG1 COL3A1 COL4A1 COQ4 CPLANE1 CPSF3 CPT2 CRPPA CSF1R CSPP1 CTNNA2 CWF19L1 DAG1 DCHS1 DENND5A DHCR7 DHFR DHX37 DISC1 DKC1 DMXL2 DOCK6 DOK7 DPAGT1 DPF2 DPH1 DPH5 DPM2 DPYSL5 DYNC1H1 DYNC2H1 DYNC2I1 DYNC2I2 EBF3 EBP EHMT1 ELN EOMES EPG5 ERCC1 ERCC5 ERCC6 ERF ERMARD ESCO2 EVC EVC2 EXOC2 EXOC7 EXOSC1 EXOSC8 EZH2 FAM149B1 FANCB FANCL FAR1 FAT4 FDXR FGFR1 FGFR2 FIG4 FKRP FKTN FLNA FLVCR2 FOXC1 FRMD4A FTO GEMIN4 GFM2 GJB2 GJB6 GLI3 GMPPB GOT2 GPAA1 GPC3 GPC4 GPHN GPSM2 GPX4 GRIA3 GRM1 GTPBP2 H19-ICR H3-3A HDAC6 HERC1 HHAT HNRNPH1 HNRNPH2 HNRNPR HRAS HYLS1 IER3IP1 IFT172 IFT80 IGF2 INPP5E INPP5K INTS1 INTS8 ITPR1 JAM3 KATNIP KCNQ1 KCNQ1OT1 KIAA0586 KIAA0753 KIDINS220 KIF14 KIF7 KMT2C KRAS L1CAM LAMA1 LAMB1 LARGE1 LETM1 LRRC32 MAB21L1 MACF1 MAN1B1 MAN2C1 MAP2K2 MAPK8IP3 MAPKAPK5 MARS2 MAST1 MBD5 MBTPS2 MDH1 MFSD2A MICOS13 MID1 MINPP1 MKS1 MLXIPL MPL MRE11 MSTO1 MTM1 MUSK MYO5A MYOD1 NCAPG2 NDE1 NDUFA6 NEK1 NFIX NODAL NONO NPHP1 NPHP3 NRAS NSD1 NSRP1 NUP37 NUP88 OCLN OFD1 OPHN1 OTUD5 OXR1 PACS1 PAFAH1B1 PARN PCGF2 PCLO PDE6D PDHB PGAP1 PHGDH PI4KA PIBF1 PIEZO2 PIGA PIGG PIGN PIGT PIGU PLCH1 PLG PLP1 PMM2 PMPCA POLR3A POMGNT1 POMGNT2 POMK POMT1 POMT2 POU4F1 PPFIBP1 PPIL1 PPP1CB PPP1R15B PPP1R21 PPP2R1A PRDM13 PRKDC PSAT1 PTEN PTF1A PTRH2 RAB11B RAB18 RAB3GAP1 RAB3GAP2 RAC1 RAPSN RARS2 RBBP8 RBM10 RBM8A RELN RERE RHOBTB2 RNF113A RNU4ATAC ROBO3 ROGDI RORA RPE65 RPGRIP1 RPGRIP1L RPL10 RTEL1 RTTN RXYLT1 SACS SASS6 SEMA3E SEMA6B SEPSECS SETD2 SHQ1 SIL1 SIX3 SLC18A3 SLC1A3 SLC25A1 SLC25A19 SLC25A24 SLC25A46 SLC35A2 SMARCA4 SMARCB1 SMARCC2 SMARCD1 SMARCE1 SMG9 SMPD4 SNX14 SON SOX11 SOX4 SRD5A3 SRPX2 STAG2 STAT2 STUB1 SUFU SUOX SYT2 TAF1 TAPT1 TBC1D20 TBC1D24 TBCK TCTN1 TCTN2 TCTN3 TERC TERT THG1L THOC2 TINF2 TKFC TMCO1 TMEM107 TMEM138 TMEM216 TMEM218 TMEM231 TMEM237 TMEM67 TMTC3 TNPO2 TOE1 TOGARAM1 TOPORS TP53RK TRAPPC9 TRIP13 TRMT10A TRRAP TSEN15 TSEN2 TSEN34 TSEN54 TUBA1A TUBB TUBB2B TUBB3 TUBGCP6 TWIST1 TXNDC15 UFSP2 USP18 USP9X VAC14 VARS2 VLDLR VPS13B VPS35L VPS4A VPS51 VRK1 WAC WARS2 WASHC5 WDR26 WDR35 WDR73 WDR81 WLS WNT1 YME1L1 ZBTB11 ZEB2 ZIC1 ZIC3 ZNF292 ZNF335 ZNF423

Diseases (457) :OMIM:613163 OMIM:616553 ORPHA:3322 ORPHA:101070 ORPHA:98889 OMIM:606854 OMIM:619297 ORPHA:313772 ORPHA:88618 ORPHA:475 OMIM:608629 ORPHA:220493 ORPHA:79324 ORPHA:79321 ORPHA:79320 OMIM:613451 OMIM:304340 OMIM:618677 ORPHA:821 OMIM:617523 ORPHA:1465 OMIM:614607 OMIM:135900 OMIM:618161 OMIM:617622 ORPHA:401815 OMIM:615574 OMIM:608716 ORPHA:97297 OMIM:605039 ORPHA:352577 OMIM:615485 OMIM:618810 OMIM:601238 ORPHA:94122 OMIM:617584 OMIM:619422 OMIM:618494 ORPHA:314978 OMIM:615228 OMIM:619971 ORPHA:357074 OMIM:219200 ORPHA:2834 ORPHA:79500 OMIM:210600 ORPHA:98756 OMIM:615181 ORPHA:899 ORPHA:79332 OMIM:607091 OMIM:615287 ORPHA:564 OMIM:614175 OMIM:300166 OMIM:618291 OMIM:617822 ORPHA:139471 OMIM:607932 ORPHA:444072 OMIM:616202 ORPHA:1052 OMIM:257300 ORPHA:434179 OMIM:615948 OMIM:618087 OMIM:614756 ORPHA:314647 OMIM:616672 OMIM:300749 ORPHA:163937 OMIM:619111 ORPHA:1454 ORPHA:2318 ORPHA:7 OMIM:300963 OMIM:619123 OMIM:619302 ORPHA:487796 OMIM:616737 OMIM:619841 OMIM:616342 OMIM:130650 OMIM:616051 OMIM:243605 OMIM:616781 OMIM:616300 OMIM:614845 OMIM:611134 OMIM:236500 ORPHA:138 OMIM:614961 OMIM:617090 OMIM:619512 OMIM:618266 ORPHA:263508 OMIM:618343 OMIM:616276 ORPHA:2754 OMIM:277170 OMIM:619876 ORPHA:228308 ORPHA:228305 OMIM:614643 OMIM:618476 ORPHA:397715 OMIM:618174 ORPHA:453521 OMIM:616127 ORPHA:370997 OMIM:616538 ORPHA:314679 OMIM:617281 OMIM:270400 OMIM:613839 OMIM:618731 ORPHA:171703 OMIM:305000 OMIM:616113 ORPHA:453533 OMIM:614219 ORPHA:994 ORPHA:86309 ORPHA:459061 OMIM:616901 OMIM:620070 OMIM:615042 ORPHA:329178 OMIM:619435 OMIM:614563 ORPHA:93271 OMIM:617330 OMIM:302960 ORPHA:401973 OMIM:300960 ORPHA:261652 OMIM:194050 OMIM:242840 ORPHA:1493 OMIM:610758 OMIM:616570 OMIM:214150 ORPHA:207 ORPHA:75857 ORPHA:2319 OMIM:225500 OMIM:619306 OMIM:619072 OMIM:619304 OMIM:616081 OMIM:277590 OMIM:300514 OMIM:614083 ORPHA:438178 OMIM:616154 ORPHA:543470 OMIM:613001 OMIM:101200 ORPHA:3472 OMIM:216340 ORPHA:370959 ORPHA:370968 OMIM:236670 OMIM:613153 OMIM:253800 OMIM:300049 ORPHA:90652 OMIM:225790 OMIM:601631 OMIM:602482 OMIM:616819 ORPHA:466688 OMIM:612938 OMIM:617913 ORPHA:565624 ORPHA:477 ORPHA:36 ORPHA:672 OMIM:615350 OMIM:615351 OMIM:618721 OMIM:617810 ORPHA:529665 ORPHA:373 OMIM:312870 OMIM:615501 OMIM:604213 ORPHA:93317 ORPHA:364028 OMIM:614831 OMIM:617988 OMIM:619720 ORPHA:163966 ORPHA:457359 OMIM:600092 OMIM:620083 OMIM:300986 OMIM:620073 ORPHA:2612 OMIM:236680 OMIM:614231 OMIM:615630 OMIM:213300 ORPHA:559 OMIM:618571 OMIM:618572 OMIM:206700 OMIM:117360 OMIM:613730 OMIM:616784 OMIM:616546 OMIM:619476 OMIM:619501 OMIM:616258 OMIM:304100 ORPHA:1497 ORPHA:370022 OMIM:615960 ORPHA:352682 OMIM:615191 OMIM:613154 OMIM:608840 OMIM:620089 OMIM:619074 OMIM:618479 OMIM:618325 ORPHA:397941 OMIM:614202 OMIM:619775 OMIM:615280 OMIM:618443 OMIM:619869 ORPHA:314603 OMIM:618273 OMIM:156200 ORPHA:2273 OMIM:618959 OMIM:616486 OMIM:618329 ORPHA:2745 OMIM:300000 ORPHA:284339 OMIM:619527 OMIM:249000 OMIM:604498 ORPHA:251347 ORPHA:502423 OMIM:310400 OMIM:208150 ORPHA:33445 OMIM:618460 OMIM:614019 OMIM:605013 OMIM:618253 OMIM:263520 ORPHA:561 OMIM:602535 OMIM:270100 ORPHA:466791 OMIM:300967 OMIM:609583 ORPHA:220497 OMIM:267010 ORPHA:3032 OMIM:208540 OMIM:249400 OMIM:620001 OMIM:618179 OMIM:251290 OMIM:300804 ORPHA:2750 OMIM:300486 ORPHA:137831 OMIM:301056 OMIM:213000 ORPHA:329224 OMIM:615009 OMIM:607432 ORPHA:95232 OMIM:616353 OMIM:618371 OMIM:608027 ORPHA:255138 OMIM:615802 OMIM:256520 OMIM:619708 OMIM:616531 OMIM:248700 ORPHA:2461 OMIM:300868 ORPHA:488635 OMIM:616917 ORPHA:2059 OMIM:615398 OMIM:618590 OMIM:619895 ORPHA:722 OMIM:217090 ORPHA:280210 OMIM:212065 ORPHA:79318 OMIM:213200 ORPHA:447896 OMIM:264090 ORPHA:3455 OMIM:253280 OMIM:613151 OMIM:614830 OMIM:615249 OMIM:613155 OMIM:613150 OMIM:613156 OMIM:620024 OMIM:619301 OMIM:617506 ORPHA:391408 OMIM:619383 ORPHA:457284 OMIM:619909 OMIM:619761 OMIM:615966 OMIM:616038 OMIM:610992 ORPHA:284417 OMIM:609069 ORPHA:65288 ORPHA:456312 OMIM:617807 ORPHA:2510 OMIM:600118 OMIM:617751 ORPHA:500159 OMIM:611523 OMIM:606744 OMIM:311900 ORPHA:2886 OMIM:274000 OMIM:257320 OMIM:616975 ORPHA:494344 OMIM:618004 OMIM:300953 OMIM:210710 OMIM:607313 OMIM:226750 OMIM:618060 OMIM:204100 OMIM:300998 ORPHA:459070 OMIM:615190 ORPHA:468631 ORPHA:98 OMIM:616402 OMIM:618876 ORPHA:2524 OMIM:619922 OMIM:157170 OMIM:612656 OMIM:615182 ORPHA:99742 OMIM:607196 OMIM:612289 OMIM:619303 OMIM:300896 ORPHA:356961 OMIM:614609 OMIM:614608 OMIM:616938 OMIM:616920 OMIM:618622 OMIM:616354 ORPHA:500150 OMIM:617140 OMIM:612379 ORPHA:521258 OMIM:618886 ORPHA:412057 OMIM:615768 OMIM:272300 OMIM:619461 OMIM:300966 OMIM:616897 OMIM:220500 OMIM:616900 OMIM:614173 OMIM:616654 OMIM:127550 OMIM:613989 OMIM:618800 OMIM:300957 OMIM:613990 OMIM:268130 OMIM:618805 ORPHA:1394 OMIM:617562 OMIM:614465 OMIM:603194 OMIM:619562 ORPHA:2752 OMIM:614424 OMIM:216360 OMIM:610688 OMIM:607361 OMIM:617255 OMIM:619556 OMIM:614969 OMIM:619185 OMIM:617730 ORPHA:352530 OMIM:613192 OMIM:618454 OMIM:617026 OMIM:612389 OMIM:612390 ORPHA:166063 OMIM:277470 OMIM:225753 OMIM:610204 OMIM:611603 ORPHA:171680 ORPHA:467166 OMIM:615771 OMIM:156610 OMIM:610031 ORPHA:300570 OMIM:251270 OMIM:617746 OMIM:620028 OMIM:617397 OMIM:300968 ORPHA:480880 OMIM:615917 OMIM:224050 OMIM:216550 OMIM:619135 OMIM:619273 OMIM:618606 OMIM:607596 ORPHA:284169 ORPHA:572798 OMIM:220210 ORPHA:513456 OMIM:251300 OMIM:610185 OMIM:617967 OMIM:619648 OMIM:615220 OMIM:617302 OMIM:618383 ORPHA:261552 ORPHA:261537 OMIM:616602 OMIM:618736 OMIM:306955 OMIM:619188 OMIM:615095 OMIM:614844

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.

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