Human Phenotype Ontology 
Grandparent Node:
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Abdominal symptom (HP:0011458)help
Parent Node:
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Feeding difficulties (HP:0011968)help
..Starting node
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Feeding difficulties in infancy (HP:0008872)help
Term ID: 8872
Name: Feeding difficulties in infancy
Synonym:
Definition: Impaired feeding performance of an infant as manifested by difficulties such as weak and ineffective sucking, brief bursts of sucking, and falling asleep during sucking. There may be difficulties with chewing or maintaining attention.
Comments:
Reference: HP:0008872
Genes and Diseases:
 
       Child Nodes:
........expandPoor suck (HP:0002033) help
........expandNasal regurgitation (HP:0011469) help
........expandNasogastric tube feeding in infancy (HP:0011470) help
........expandGastrostomy tube feeding in infancy (HP:0011471) help
........expandGastrojejunal tube feeding in infancy (HP:0030884) help

 Sister Nodes: 
..expandDelayed self-feeding during toddler years (HP:0012381) help
..expandNasogastric tube feeding (HP:0040288) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008872HP:0008872Feeding difficulties in infancy0A2ML1 CL E G H144568648ORPHA12149223336610627
HP:0008872HP:0008872Feeding difficulties in infancy0ACADS CL E G H35201470Deficiency of butyryl-CoA dehydrogenase201470C0342783OMIM18521690606885
HP:0008872HP:0008872Feeding difficulties in infancy0ACTA1 CL E G H58161800Nemaline myopathy 3161800C3711389OMIM1217272129102610
HP:0008872HP:0008872Feeding difficulties in infancy0AHI1 CL E G H54806475Acquired hypoprothrombinemiaORPHA19642221575608894
HP:0008872HP:0008872Feeding difficulties in infancy0APC2 CL E G H10297821ORPHA1315624036612034
HP:0008872HP:0008872Feeding difficulties in infancy0AQP2 CL E G H359125800Nephrogenic diabetes insipidus, autosomal125800C1563706OMIM166176634107777
HP:0008872HP:0008872Feeding difficulties in infancy0ARID1A CL E G H82891465ORPHA13617511110603024
HP:0008872HP:0008872Feeding difficulties in infancy0ARID1B CL E G H574921465ORPHA118857518040614556
HP:0008872HP:0008872Feeding difficulties in infancy0ARID1B CL E G H57492135900Coffin-Siris syndrome 1135900C3281201OMIM118857518040614556
HP:0008872HP:0008872Feeding difficulties in infancy0ARID2 CL E G H1965281465ORPHA11111518037609539
HP:0008872HP:0008872Feeding difficulties in infancy0ARL13B CL E G H200894475Acquired hypoprothrombinemiaORPHA11012025419608922
HP:0008872HP:0008872Feeding difficulties in infancy0ARL3 CL E G H403475Acquired hypoprothrombinemiaORPHA1333694604695
HP:0008872HP:0008872Feeding difficulties in infancy0ARMC9 CL E G H80210475Acquired hypoprothrombinemiaORPHA11110520730617612
HP:0008872HP:0008872Feeding difficulties in infancy0ARX CL E G H170302300215Lissencephaly 2, X-linked300215C1846171OMIM19846618060300382
HP:0008872HP:0008872Feeding difficulties in infancy0ASL CL E G H435207900Argininosuccinate lyase deficiency207900C0268547OMIM1169264746608310
HP:0008872HP:0008872Feeding difficulties in infancy0ASXL2 CL E G H55252617190Shashi-Pena syndrome617190C4310672OMIM168123805612991
HP:0008872HP:0008872Feeding difficulties in infancy0ATP6V0A2 CL E G H23545219200Cutis laxa with osteodystrophy219200C0268355OMIM15630918481611716
HP:0008872HP:0008872Feeding difficulties in infancy0ATP7A CL E G H538565ORPHA1357607869300011
HP:0008872HP:0008872Feeding difficulties in infancy0AVPR2 CL E G H554304800Nephrogenic diabetes insipidus, X-linked304800C1563705OMIM1286356897300538
HP:0008872HP:0008872Feeding difficulties in infancy0B3GLCT CL E G H145173709ORPHA11518120207610308
HP:0008872HP:0008872Feeding difficulties in infancy0B3GLCT CL E G H145173261540Peters plus syndrome261540C0796012OMIM11518120207610308
HP:0008872HP:0008872Feeding difficulties in infancy0B9D1 CL E G H27077475Acquired hypoprothrombinemiaORPHA11015824123614144
HP:0008872HP:0008872Feeding difficulties in infancy0BCKDHA CL E G H593248600Maple syrup urine disease248600C0024776OMIM1101255986608348
HP:0008872HP:0008872Feeding difficulties in infancy0BCKDHB CL E G H594248600Maple syrup urine disease248600C0024776OMIM1115319987248611
HP:0008872HP:0008872Feeding difficulties in infancy0BCS1L CL E G H617124000Mitochondrial complex III deficiency124000C1852372OMIM1371741020603647
HP:0008872HP:0008872Feeding difficulties in infancy0BIN1 CL E G H274255200Autosomal recessive centronuclear myopathy255200C0410204OMIM1173151052601248
HP:0008872HP:0008872Feeding difficulties in infancy0BRAF CL E G H673648ORPHA1684901097164757
HP:0008872HP:0008872Feeding difficulties in infancy0BRAF CL E G H673115150Cardiofaciocutaneous syndrome 1115150CN029449OMIM1684901097164757
HP:0008872HP:0008872Feeding difficulties in infancy0BRAF CL E G H6731340Chromosome 4, monosomy 4qC0265404ORPHA1684901097164757
HP:0008872HP:0008872Feeding difficulties in infancy0BTD CL E G H686253260Biotinidase deficiency253260C0220754OMIM12483711122609019
HP:0008872HP:0008872Feeding difficulties in infancy0BUB1B CL E G H701257300Mosaic variegated aneuploidy syndrome 1257300CN031748OMIM1293231149602860
HP:0008872HP:0008872Feeding difficulties in infancy0CASR CL E G H846239200Neonatal severe hyperparathyroidism239200C1832615OMIM14109551514601199
HP:0008872HP:0008872Feeding difficulties in infancy0CC2D2A CL E G H575451454Common atrioventricular canalC0221215ORPHA19658429253612013
HP:0008872HP:0008872Feeding difficulties in infancy0CEP104 CL E G H9731475Acquired hypoprothrombinemiaORPHA1715224866616690
HP:0008872HP:0008872Feeding difficulties in infancy0CEP120 CL E G H153241475Acquired hypoprothrombinemiaORPHA198726690613446
HP:0008872HP:0008872Feeding difficulties in infancy0CEP41 CL E G H95681475Acquired hypoprothrombinemiaORPHA11123212370610523
HP:0008872HP:0008872Feeding difficulties in infancy0CHD7 CL E G H55636138ORPHA1884126620626608892
HP:0008872HP:0008872Feeding difficulties in infancy0CHRNE CL E G H1145605809Myasthenic syndrome, congenital, 4a, slow-channel605809C1853949OMIM11383871966100725
HP:0008872HP:0008872Feeding difficulties in infancy0CISD2 CL E G H4938563463ORPHA142324212611507
HP:0008872HP:0008872Feeding difficulties in infancy0CLCF1 CL E G H23529610313Cold-induced sweating syndrome 2610313C1853198OMIM142517412607672
HP:0008872HP:0008872Feeding difficulties in infancy0CLDN16 CL E G H10686248250Primary hypomagnesemia248250C0268448OMIM1651882037603959
HP:0008872HP:0008872Feeding difficulties in infancy0COL11A2 CL E G H13021427ORPHA1594712187120290
HP:0008872HP:0008872Feeding difficulties in infancy0COL6A1 CL E G H1291254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM113710072211120220
HP:0008872HP:0008872Feeding difficulties in infancy0COL6A2 CL E G H1292254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM119111482212120240
HP:0008872HP:0008872Feeding difficulties in infancy0COL6A3 CL E G H1293254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM114316342213120250
HP:0008872HP:0008872Feeding difficulties in infancy0COLQ CL E G H8292603034Endplate acetylcholinesterase deficiency603034C1864233OMIM1702622226603033
HP:0008872HP:0008872Feeding difficulties in infancy0CPLANE1 CL E G H652502754ORPHA111859425801614571
HP:0008872HP:0008872Feeding difficulties in infancy0CPLANE1 CL E G H65250475Acquired hypoprothrombinemiaORPHA111859425801614571
HP:0008872HP:0008872Feeding difficulties in infancy0CPT1A CL E G H1374255120Carnitine palmitoyltransferase I deficiency255120C0342789OMIM1532392328600528
HP:0008872HP:0008872Feeding difficulties in infancy0CPT2 CL E G H1376608836Carnitine palmitoyltransferase II deficiency, lethal neonatal608836C1833518OMIM11133662330600650
HP:0008872HP:0008872Feeding difficulties in infancy0CREBBP CL E G H1387180849Rubinstein-Taybi syndrome180849C0035934OMIM13647552348600140
HP:0008872HP:0008872Feeding difficulties in infancy0CRLF1 CL E G H9244272430Cold-induced sweating syndrome 1272430C1848947OMIM137562364604237
HP:0008872HP:0008872Feeding difficulties in infancy0CSPP1 CL E G H79848475Acquired hypoprothrombinemiaORPHA12725726193611654
HP:0008872HP:0008872Feeding difficulties in infancy0CYP11B2 CL E G H1585203400Corticosterone methyloxidase type 1 deficiency203400CN074214OMIM1552212592124080
HP:0008872HP:0008872Feeding difficulties in infancy0DBT CL E G H1629248600Maple syrup urine disease248600C0024776OMIM1783402698248610
HP:0008872HP:0008872Feeding difficulties in infancy0DDC CL E G H1644608643Deficiency of aromatic-L-amino-acid decarboxylase608643C1291564OMIM1591162719107930
HP:0008872HP:0008872Feeding difficulties in infancy0DEAF1 CL E G H10522819ORPHA11712914677602635
HP:0008872HP:0008872Feeding difficulties in infancy0DGUOK CL E G H1716251880Mitochondrial DNA-depletion syndrome 3, hepatocerebral251880C3151513OMIM1641222858601465
HP:0008872HP:0008872Feeding difficulties in infancy0DHCR7 CL E G H1717818ORPHA12183762860602858
HP:0008872HP:0008872Feeding difficulties in infancy0DLEC1 CL E G H994099977ORPHA13382899604050
HP:0008872HP:0008872Feeding difficulties in infancy0DMPK CL E G H1760160900Steinert myotonic dystrophy syndrome160900C3250443OMIM182332933605377
HP:0008872HP:0008872Feeding difficulties in infancy0DPF2 CL E G H59771465ORPHA19149964601671
HP:0008872HP:0008872Feeding difficulties in infancy0DPYS CL E G H1807222748Dihydropyrimidinase deficiency222748C0342803OMIM1301083013613326
HP:0008872HP:0008872Feeding difficulties in infancy0EED CL E G H87263447ORPHA19493188605984
HP:0008872HP:0008872Feeding difficulties in infancy0EFTUD2 CL E G H9343610536Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate610536C1864652OMIM110112430858603892
HP:0008872HP:0008872Feeding difficulties in infancy0ELN CL E G H2006194050Williams syndrome194050C0175702OMIM11275233327130160
HP:0008872HP:0008872Feeding difficulties in infancy0ELP1 CL E G H85181764ORPHA166605959603722
HP:0008872HP:0008872Feeding difficulties in infancy0ELP1 CL E G H8518223900Familial dysautonomia223900C0013364OMIM166605959603722
HP:0008872HP:0008872Feeding difficulties in infancy0EMG1 CL E G H104361270ORPHA115916912611531
HP:0008872HP:0008872Feeding difficulties in infancy0EP300 CL E G H2033180849Rubinstein-Taybi syndrome180849C0035934OMIM11074153373602700
HP:0008872HP:0008872Feeding difficulties in infancy0ERCC1 CL E G H20671466ORPHA18533433126380
HP:0008872HP:0008872Feeding difficulties in infancy0ERCC2 CL E G H20681466ORPHA11082273434126340
HP:0008872HP:0008872Feeding difficulties in infancy0ERCC5 CL E G H20731466ORPHA1592633437133530
HP:0008872HP:0008872Feeding difficulties in infancy0ERCC6 CL E G H20741466ORPHA11404993438609413
HP:0008872HP:0008872Feeding difficulties in infancy0EZH2 CL E G H21463447ORPHA1422353527601573
HP:0008872HP:0008872Feeding difficulties in infancy0FGFR2 CL E G H226387ORPHA11593363689176943
HP:0008872HP:0008872Feeding difficulties in infancy0FKRP CL E G H79147606612Congenital muscular dystrophy-dystroglycanopathy (with or without mental retardation) type B5606612C1847759OMIM114140217997606596
HP:0008872HP:0008872Feeding difficulties in infancy0FLCN CL E G H201163610883Chromosome 17, trisomy 17p11 2610883C2931246OMIM1215103627310607273
HP:0008872HP:0008872Feeding difficulties in infancy0FLI1 CL E G H23132308Fetal minoxidil syndromeORPHA171253749193067
HP:0008872HP:0008872Feeding difficulties in infancy0FLII CL E G H2314819ORPHA121533750600362
HP:0008872HP:0008872Feeding difficulties in infancy0FLNA CL E G H2316300048Intestinal pseudoobstruction neuronal chronic idiopathic X-linked300048C2746068OMIM127114723754300017
HP:0008872HP:0008872Feeding difficulties in infancy0GABRD CL E G H25631606ORPHA172784084137163
HP:0008872HP:0008872Feeding difficulties in infancy0GCDH CL E G H263925ORPHA12443374189608801
HP:0008872HP:0008872Feeding difficulties in infancy0HADH CL E G H3033231530Deficiency of 3-hydroxyacyl-CoA dehydrogenase231530C1291230OMIM126944799601609
HP:0008872HP:0008872Feeding difficulties in infancy0HDAC8 CL E G H55869199Cardiac hydatid cysts with intracavitary expansionORPHA15622713315300269
HP:0008872HP:0008872Feeding difficulties in infancy0HLCS CL E G H3141253270Holocarboxylase synthetase deficiency253270C0268581OMIM1493734976609018
HP:0008872HP:0008872Feeding difficulties in infancy0HSD17B4 CL E G H3295261515Bifunctional peroxisomal enzyme deficiency261515C0342870OMIM11013055213601860
HP:0008872HP:0008872Feeding difficulties in infancy0HSPD1 CL E G H3329612233Leukodystrophy, hypomyelinating, 4612233C2677109OMIM161285261118190
HP:0008872HP:0008872Feeding difficulties in infancy0HYLS1 CL E G H219844475Acquired hypoprothrombinemiaORPHA1212226558610693
HP:0008872HP:0008872Feeding difficulties in infancy0IGF2 CL E G H3481616489Growth restriction, severe, with distinctive facies616489C4225307OMIM111675466147470
HP:0008872HP:0008872Feeding difficulties in infancy0INPP5E CL E G H56623475Acquired hypoprothrombinemiaORPHA15432521474613037
HP:0008872HP:0008872Feeding difficulties in infancy0INPP5E CL E G H566231454Common atrioventricular canalC0221215ORPHA15432521474613037
HP:0008872HP:0008872Feeding difficulties in infancy0INSR CL E G H3643508Acroosteolysis dominant typeORPHA11964076091147670
HP:0008872HP:0008872Feeding difficulties in infancy0IQSEC2 CL E G H23096819ORPHA15753929059300522
HP:0008872HP:0008872Feeding difficulties in infancy0KANSL1 CL E G H284058610443Koolen-de Vries syndrome610443C1864871OMIM17284024565612452
HP:0008872HP:0008872Feeding difficulties in infancy0KAT6B CL E G H23522648ORPHA17622817582605880
HP:0008872HP:0008872Feeding difficulties in infancy0KCNAB2 CL E G H85141606ORPHA15856229601142
HP:0008872HP:0008872Feeding difficulties in infancy0KCNK9 CL E G H51305612292Birk Barel mental retardation dysmorphism syndrome612292C2676770OMIM12656283605874
HP:0008872HP:0008872Feeding difficulties in infancy0KDM6A CL E G H7403147920Kabuki syndrome 1147920CN030661OMIM18131112637300128
HP:0008872HP:0008872Feeding difficulties in infancy0KDM6A CL E G H7403300867Kabuki syndrome 2300867C3275495OMIM18131112637300128
HP:0008872HP:0008872Feeding difficulties in infancy0KIAA0556 CL E G H23247475Acquired hypoprothrombinemiaORPHA1229068616650
HP:0008872HP:0008872Feeding difficulties in infancy0KIAA0586 CL E G H9786475Acquired hypoprothrombinemiaORPHA13115519960610178
HP:0008872HP:0008872Feeding difficulties in infancy0KIAA0753 CL E G H98512754ORPHA176529110617112
HP:0008872HP:0008872Feeding difficulties in infancy0KIF1A CL E G H547201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1431059888601255
HP:0008872HP:0008872Feeding difficulties in infancy0KIF7 CL E G H3746542754ORPHA14538630497611254
HP:0008872HP:0008872Feeding difficulties in infancy0KMT2A CL E G H4297199Cardiac hydatid cysts with intracavitary expansionORPHA11273797132159555
HP:0008872HP:0008872Feeding difficulties in infancy0KMT2D CL E G H8085147920Kabuki syndrome 1147920CN030661OMIM171213507133602113
HP:0008872HP:0008872Feeding difficulties in infancy0KRAS CL E G H3845648ORPHA1452746407190070
HP:0008872HP:0008872Feeding difficulties in infancy0KRAS CL E G H38451340Chromosome 4, monosomy 4qC0265404ORPHA1452746407190070
HP:0008872HP:0008872Feeding difficulties in infancy0LAMA2 CL E G H3908607855Merosin deficient congenital muscular dystrophy607855C1263858OMIM138014996482156225
HP:0008872HP:0008872Feeding difficulties in infancy0LIFR CL E G H39773206ORPHA1323466597151443
HP:0008872HP:0008872Feeding difficulties in infancy0LMBRD1 CL E G H5578879284ORPHA1910423038612625
HP:0008872HP:0008872Feeding difficulties in infancy0LMBRD1 CL E G H55788277380METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE277380C1848578OMIM1910423038612625
HP:0008872HP:0008872Feeding difficulties in infancy0LZTR1 CL E G H8216648ORPHA1866996742600574
HP:0008872HP:0008872Feeding difficulties in infancy0MAP2K1 CL E G H56041340Chromosome 4, monosomy 4qC0265404ORPHA1232136840176872
HP:0008872HP:0008872Feeding difficulties in infancy0MAP2K2 CL E G H56051340Chromosome 4, monosomy 4qC0265404ORPHA1353386842601263
HP:0008872HP:0008872Feeding difficulties in infancy0MBD5 CL E G H55777156200Mental retardation, autosomal dominant 1156200C1969562OMIM19166420444611472
HP:0008872HP:0008872Feeding difficulties in infancy0MCCC1 CL E G H569222102003 Methylcrotonyl-CoA carboxylase 1 deficiency210200CN028786OMIM11082736936609010
HP:0008872HP:0008872Feeding difficulties in infancy0MECP2 CL E G H4204300673Severe neonatal-onset encephalopathy with microcephaly300673C1968556OMIM1105014426990300005
HP:0008872HP:0008872Feeding difficulties in infancy0MKS1 CL E G H54903475Acquired hypoprothrombinemiaORPHA1523347121609883
HP:0008872HP:0008872Feeding difficulties in infancy0MLXIPL CL E G H51085194050Williams syndrome194050C0175702OMIM1619712744605678
HP:0008872HP:0008872Feeding difficulties in infancy0MMAA CL E G H166785251100Methylmalonic aciduria cblA type251100C1855109OMIM17626318871607481
HP:0008872HP:0008872Feeding difficulties in infancy0MMAB CL E G H326625251110Methylmalonic aciduria cblB type251110C1855102OMIM14225619331607568
HP:0008872HP:0008872Feeding difficulties in infancy0MMACHC CL E G H25974277400Methylmalonic acidemia with homocystinuria277400C1848561OMIM19527424525609831
HP:0008872HP:0008872Feeding difficulties in infancy0MOCS1 CL E G H4337252150Molybdenum cofactor deficiency, complementation group A252150C1854988OMIM1351817190603707
HP:0008872HP:0008872Feeding difficulties in infancy0MOGS CL E G H7841606056Congenital disorder of glycosylation type 2B606056C1853736OMIM1817324862601336
HP:0008872HP:0008872Feeding difficulties in infancy0MRPS16 CL E G H51021610498Combined oxidative phosphorylation deficiency 2610498C1864843OMIM115114048609204
HP:0008872HP:0008872Feeding difficulties in infancy0MTR CL E G H4548250940METHYLCOBALAMIN DEFICIENCY, cblG TYPE250940C1855128OMIM1444287468156570
HP:0008872HP:0008872Feeding difficulties in infancy0MYH3 CL E G H46212053Ectodermal dysplasia neurosensory deafnessORPHA1453157573160720
HP:0008872HP:0008872Feeding difficulties in infancy0MYH3 CL E G H4621193700Freeman-Sheldon syndrome193700C0265224OMIM1453157573160720
HP:0008872HP:0008872Feeding difficulties in infancy0NALCN CL E G H2592322053Ectodermal dysplasia neurosensory deafnessORPHA16524719082611549
HP:0008872HP:0008872Feeding difficulties in infancy0NDUFS4 CL E G H4724252010Mitochondrial complex I deficiency252010C1838979OMIM117697711602694
HP:0008872HP:0008872Feeding difficulties in infancy0NIPBL CL E G H25836199Cardiac hydatid cysts with intracavitary expansionORPHA143780928862608667
HP:0008872HP:0008872Feeding difficulties in infancy0NRAS CL E G H4893648ORPHA1141817989164790
HP:0008872HP:0008872Feeding difficulties in infancy0NSD1 CL E G H64324821ORPHA152589614234606681
HP:0008872HP:0008872Feeding difficulties in infancy0NSD1 CL E G H643243447ORPHA152589614234606681
HP:0008872HP:0008872Feeding difficulties in infancy0OCRL CL E G H4952534Acute myeloblastic leukemia without maturationORPHA12643428108300535
HP:0008872HP:0008872Feeding difficulties in infancy0OFD1 CL E G H84812754ORPHA11625102567300170
HP:0008872HP:0008872Feeding difficulties in infancy0OFD1 CL E G H8481300804Joubert syndrome 10300804C2749019OMIM11625102567300170
HP:0008872HP:0008872Feeding difficulties in infancy0OPA1 CL E G H4976616896Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)616896C4225163OMIM13944418140605290
HP:0008872HP:0008872Feeding difficulties in infancy0ORC1 CL E G H4998224690Meier-Gorlin syndrome 1224690CN030358OMIM1121038487601902
HP:0008872HP:0008872Feeding difficulties in infancy0PANK2 CL E G H80025234200Pigmentary pallidal degeneration234200C0018523OMIM118219215894606157
HP:0008872HP:0008872Feeding difficulties in infancy0PAX8 CL E G H7849218700Thyroid dysgenesis218700C1563716OMIM1511438622167415
HP:0008872HP:0008872Feeding difficulties in infancy0PCCA CL E G H5095606054Propionyl-CoA carboxylase deficiency606054C0268579OMIM11493878653232000
HP:0008872HP:0008872Feeding difficulties in infancy0PCCB CL E G H5096606054Propionyl-CoA carboxylase deficiency606054C0268579OMIM11313018654232050
HP:0008872HP:0008872Feeding difficulties in infancy0PDE6D CL E G H51472754ORPHA11398788602676
HP:0008872HP:0008872Feeding difficulties in infancy0PEX1 CL E G H5189912ORPHA11404898850602136
HP:0008872HP:0008872Feeding difficulties in infancy0PEX10 CL E G H5192912ORPHA1323478851602859
HP:0008872HP:0008872Feeding difficulties in infancy0PEX10 CL E G H5192614870Peroxisome biogenesis disorder 6A614870C3553947OMIM1323478851602859
HP:0008872HP:0008872Feeding difficulties in infancy0PEX11B CL E G H8799912ORPHA182478853603867
HP:0008872HP:0008872Feeding difficulties in infancy0PEX12 CL E G H5193912ORPHA1371818854601758
HP:0008872HP:0008872Feeding difficulties in infancy0PEX12 CL E G H5193614859Peroxisome biogenesis disorder 3A614859C3553929OMIM1371818854601758
HP:0008872HP:0008872Feeding difficulties in infancy0PEX13 CL E G H5194912ORPHA1101968855601789
HP:0008872HP:0008872Feeding difficulties in infancy0PEX14 CL E G H5195912ORPHA151768856601791
HP:0008872HP:0008872Feeding difficulties in infancy0PEX16 CL E G H9409912ORPHA1151498857603360
HP:0008872HP:0008872Feeding difficulties in infancy0PEX16 CL E G H9409614876Peroxisome biogenesis disorder 8A614876C3553959OMIM1151498857603360
HP:0008872HP:0008872Feeding difficulties in infancy0PEX19 CL E G H5824912ORPHA141339713600279
HP:0008872HP:0008872Feeding difficulties in infancy0PEX2 CL E G H5828912ORPHA1182089717170993
HP:0008872HP:0008872Feeding difficulties in infancy0PEX26 CL E G H55670912ORPHA12727722965608666
HP:0008872HP:0008872Feeding difficulties in infancy0PEX3 CL E G H8504912ORPHA1101168858603164
HP:0008872HP:0008872Feeding difficulties in infancy0PEX5 CL E G H5830912ORPHA1142809719600414
HP:0008872HP:0008872Feeding difficulties in infancy0PEX6 CL E G H5190912ORPHA11093758859601498
HP:0008872HP:0008872Feeding difficulties in infancy0PEX6 CL E G H5190614862Peroxisome biogenesis disorder 4a (zellweger)614862C3553936OMIM11093758859601498
HP:0008872HP:0008872Feeding difficulties in infancy0PHF6 CL E G H84295127ORPHA12923518145300414
HP:0008872HP:0008872Feeding difficulties in infancy0PIBF1 CL E G H10464475Acquired hypoprothrombinemiaORPHA188723352607532
HP:0008872HP:0008872Feeding difficulties in infancy0PIGN CL E G H23556280633Multiple congenital anomalies-hypotonia-seizures syndromeCN228166ORPHA1344168967606097
HP:0008872HP:0008872Feeding difficulties in infancy0PLXND1 CL E G H23129570ORPHA181049107604282
HP:0008872HP:0008872Feeding difficulties in infancy0PMM2 CL E G H5373212065Carbohydrate-deficient glycoprotein syndrome type I212065C0349653OMIM11293639115601785
HP:0008872HP:0008872Feeding difficulties in infancy0PNPO CL E G H55163610090Pyridoxal 5'-phosphate-dependent epilepsy610090C1864723OMIM13118430260603287
HP:0008872HP:0008872Feeding difficulties in infancy0PRDM16 CL E G H639761606ORPHA12167714000605557
HP:0008872HP:0008872Feeding difficulties in infancy0PRDX1 CL E G H5052277400Methylmalonic acidemia with homocystinuria277400C1848561OMIM13229352176763
HP:0008872HP:0008872Feeding difficulties in infancy0PSAT1 CL E G H29968610992Phosphoserine aminotransferase deficiency610992C1970253OMIM11032319129610936
HP:0008872HP:0008872Feeding difficulties in infancy0PTPN11 CL E G H5781648ORPHA11434759644176876
HP:0008872HP:0008872Feeding difficulties in infancy0RAB3GAP1 CL E G H229301387Cleft palate cardiac defect ectrodactylyORPHA16719317063602536
HP:0008872HP:0008872Feeding difficulties in infancy0RAB3GAP2 CL E G H257821387Cleft palate cardiac defect ectrodactylyORPHA11629417168609275
HP:0008872HP:0008872Feeding difficulties in infancy0RAB3GAP2 CL E G H25782212720Martsolf syndrome212720C0796037OMIM11629417168609275
HP:0008872HP:0008872Feeding difficulties in infancy0RAD21 CL E G H5885199Cardiac hydatid cysts with intracavitary expansionORPHA1131499811606462
HP:0008872HP:0008872Feeding difficulties in infancy0RAF1 CL E G H5894648ORPHA1545089829164760
HP:0008872HP:0008872Feeding difficulties in infancy0RAI1 CL E G H10743819ORPHA11164049834607642
HP:0008872HP:0008872Feeding difficulties in infancy0RASA2 CL E G H5922648ORPHA13739872601589
HP:0008872HP:0008872Feeding difficulties in infancy0RERE CL E G H4731606ORPHA1251619965605226
HP:0008872HP:0008872Feeding difficulties in infancy0RETREG1 CL E G H54463201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1628925964613114
HP:0008872HP:0008872Feeding difficulties in infancy0REV3L CL E G H5980570ORPHA191249968602776
HP:0008872HP:0008872Feeding difficulties in infancy0RIT1 CL E G H6016648ORPHA12610610023609591
HP:0008872HP:0008872Feeding difficulties in infancy0RNF6 CL E G H604999977ORPHA113710069604242
HP:0008872HP:0008872Feeding difficulties in infancy0RPGRIP1L CL E G H233221454Common atrioventricular canalC0221215ORPHA15143229168610937
HP:0008872HP:0008872Feeding difficulties in infancy0RPS6KA3 CL E G H6197192Karandikar Maria Kamble syndromeORPHA117130910432300075
HP:0008872HP:0008872Feeding difficulties in infancy0RRAS CL E G H6237648ORPHA127510447165090
HP:0008872HP:0008872Feeding difficulties in infancy0RYR1 CL E G H6261255320Minicore myopathy255320C1850674OMIM1688309410483180901
HP:0008872HP:0008872Feeding difficulties in infancy0SAMHD1 CL E G H25939612952Aicardi Goutieres syndrome 5612952C2749659OMIM15720015925606754
HP:0008872HP:0008872Feeding difficulties in infancy0SCN9A CL E G H6335201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1129109210597603415
HP:0008872HP:0008872Feeding difficulties in infancy0SCNN1A CL E G H6337264350Pseudohypoaldosteronism type 1 autosomal recessive264350C1449843OMIM14917110599600228
HP:0008872HP:0008872Feeding difficulties in infancy0SCNN1B CL E G H6338264350Pseudohypoaldosteronism type 1 autosomal recessive264350C1449843OMIM15014510600600760
HP:0008872HP:0008872Feeding difficulties in infancy0SCNN1G CL E G H6340264350Pseudohypoaldosteronism type 1 autosomal recessive264350C1449843OMIM12312110602600761
HP:0008872HP:0008872Feeding difficulties in infancy0SCO2 CL E G H9997604377Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency604377C1858424OMIM13727510604604272
HP:0008872HP:0008872Feeding difficulties in infancy0SEMA3E CL E G H9723138ORPHA1416010727608166
HP:0008872HP:0008872Feeding difficulties in infancy0SETD2 CL E G H29072821ORPHA11943318420612778
HP:0008872HP:0008872Feeding difficulties in infancy0SETD5 CL E G H55209199Cardiac hydatid cysts with intracavitary expansionORPHA13823625566615743
HP:0008872HP:0008872Feeding difficulties in infancy0SIN3A CL E G H25942613406Witteveen-kolk syndrome613406C3150674OMIM11611619353607776
HP:0008872HP:0008872Feeding difficulties in infancy0SKI CL E G H64971606ORPHA12450210896164780
HP:0008872HP:0008872Feeding difficulties in infancy0SLC16A2 CL E G H6567300523Allan-Herndon-Dudley syndrome300523C0795889OMIM18825710923300095
HP:0008872HP:0008872Feeding difficulties in infancy0SLC46A1 CL E G H113235229050Congenital defect of folate absorption229050C0342705OMIM12316630521611672
HP:0008872HP:0008872Feeding difficulties in infancy0SLC6A8 CL E G H6535300352Creatine deficiency, X-linked300352C1845862OMIM113954211055300036
HP:0008872HP:0008872Feeding difficulties in infancy0SLC9A6 CL E G H1047985278ORPHA12835111079300231
HP:0008872HP:0008872Feeding difficulties in infancy0SMARCA4 CL E G H65971465ORPHA157247311100603254
HP:0008872HP:0008872Feeding difficulties in infancy0SMARCB1 CL E G H65981465ORPHA111948211103601607
HP:0008872HP:0008872Feeding difficulties in infancy0SMARCE1 CL E G H66051465ORPHA11328711109603111
HP:0008872HP:0008872Feeding difficulties in infancy0SMC1A CL E G H8243199Cardiac hydatid cysts with intracavitary expansionORPHA110048411111300040
HP:0008872HP:0008872Feeding difficulties in infancy0SMC3 CL E G H9126199Cardiac hydatid cysts with intracavitary expansionORPHA1282132468606062
HP:0008872HP:0008872Feeding difficulties in infancy0SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM1282132468606062
HP:0008872HP:0008872Feeding difficulties in infancy0SMPD1 CL E G H6609257200Niemann-Pick disease, type A257200C0268242OMIM125439711120607608
HP:0008872HP:0008872Feeding difficulties in infancy0SOS1 CL E G H6654648ORPHA17566511187182530
HP:0008872HP:0008872Feeding difficulties in infancy0SOS2 CL E G H6655648ORPHA1632411188601247
HP:0008872HP:0008872Feeding difficulties in infancy0SOX11 CL E G H66641465ORPHA1147011191600898
HP:0008872HP:0008872Feeding difficulties in infancy0SRCAP CL E G H108472044Ectodermal dysplasia Berlin typeORPHA14424516974611421
HP:0008872HP:0008872Feeding difficulties in infancy0ST3GAL5 CL E G H8869609056Amish infantile epilepsy syndrome609056C1836824OMIM1716310872604402
HP:0008872HP:0008872Feeding difficulties in infancy0SUCLA2 CL E G H8803612073Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)612073C2749864OMIM12918911448603921
HP:0008872HP:0008872Feeding difficulties in infancy0SUZ12 CL E G H235123447ORPHA137217101606245
HP:0008872HP:0008872Feeding difficulties in infancy0TCTN1 CL E G H79600475Acquired hypoprothrombinemiaORPHA1611626113609863
HP:0008872HP:0008872Feeding difficulties in infancy0TCTN2 CL E G H79867475Acquired hypoprothrombinemiaORPHA11520325774613846
HP:0008872HP:0008872Feeding difficulties in infancy0TCTN3 CL E G H261232754ORPHA1129524519613847
HP:0008872HP:0008872Feeding difficulties in infancy0TGFBR2 CL E G H704899977ORPHA114857211773190182
HP:0008872HP:0008872Feeding difficulties in infancy0TK2 CL E G H7084254875ORPHA16020611831188250
HP:0008872HP:0008872Feeding difficulties in infancy0TMEM216 CL E G H512592754ORPHA1810925018613277
HP:0008872HP:0008872Feeding difficulties in infancy0TMEM237 CL E G H65062475Acquired hypoprothrombinemiaORPHA11122114432614423
HP:0008872HP:0008872Feeding difficulties in infancy0TMEM67 CL E G H91147475Acquired hypoprothrombinemiaORPHA117431628396609884
HP:0008872HP:0008872Feeding difficulties in infancy0TMEM67 CL E G H911471454Common atrioventricular canalC0221215ORPHA117431628396609884
HP:0008872HP:0008872Feeding difficulties in infancy0TPM2 CL E G H7169609285Nemaline myopathy 4609285C1836447OMIM14019912011190990
HP:0008872HP:0008872Feeding difficulties in infancy0TREX1 CL E G H11277225750Aicardi Goutieres syndrome 1225750C0796126OMIM17115312269606609
HP:0008872HP:0008872Feeding difficulties in infancy0TRMU CL E G H55687613070Liver failure acute infantile613070C3278664OMIM12329625481610230
HP:0008872HP:0008872Feeding difficulties in infancy0TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM12117627561608755
HP:0008872HP:0008872Feeding difficulties in infancy0TSFM CL E G H10102610505Combined oxidative phosphorylation deficiency 3610505C1864840OMIM1710312367604723
HP:0008872HP:0008872Feeding difficulties in infancy0TSPYL1 CL E G H7259608800Sudden infant death with dysgenesis of the testes syndrome608800C1837371OMIM183212382604714
HP:0008872HP:0008872Feeding difficulties in infancy0TUBB3 CL E G H10381300570ORPHA12615520772602661
HP:0008872HP:0008872Feeding difficulties in infancy0TXNL4A CL E G H10907608572Burn-McKeown syndrome608572C1837822OMIM11317630551611595
HP:0008872HP:0008872Feeding difficulties in infancy0UBE3A CL E G H7337105830Angelman syndrome105830C0162635OMIM120275912496601623
HP:0008872HP:0008872Feeding difficulties in infancy0VPS13B CL E G H157680193ORPHA121316062183607817
HP:0008872HP:0008872Feeding difficulties in infancy0VPS13B CL E G H157680216550Cohen syndrome216550C0265223OMIM121316062183607817
HP:0008872HP:0008872Feeding difficulties in infancy0VRK1 CL E G H7443607596Pontocerebellar hypoplasia type 1A607596CN032785OMIM11018612718602168
HP:0008872HP:0008872Feeding difficulties in infancy0WFS1 CL E G H74663463ORPHA139371412762606201
HP:0008872HP:0008872Feeding difficulties in infancy0WNK1 CL E G H65125201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM11882014540605232
HP:0008872HP:0008872Feeding difficulties in infancy0WWOX CL E G H5174199977ORPHA15059612799605131
HP:0008872HP:0008872Feeding difficulties in infancy0ZNHIT3 CL E G H9326260565PEHO syndrome260565C1850055OMIM119912309604500
HP:0008872HP:0008872Feeding difficulties in infancy1A2ML1 CL E G H144568648ORPHA12149223336610627
HP:0008872HP:0008872Feeding difficulties in infancy1ACADS CL E G H35201470Deficiency of butyryl-CoA dehydrogenase201470C0342783OMIM18521690606885
HP:0008872HP:0008872Feeding difficulties in infancy1ACTA1 CL E G H58161800Nemaline myopathy 3161800C3711389OMIM1217272129102610
HP:0008872HP:0008872Feeding difficulties in infancy1AHI1 CL E G H54806475Acquired hypoprothrombinemiaORPHA19642221575608894
HP:0008872HP:0008872Feeding difficulties in infancy1APC2 CL E G H10297821ORPHA1315624036612034
HP:0008872HP:0008872Feeding difficulties in infancy1AQP2 CL E G H359125800Nephrogenic diabetes insipidus, autosomal125800C1563706OMIM166176634107777
HP:0008872HP:0008872Feeding difficulties in infancy1ARID1A CL E G H82891465ORPHA13617511110603024
HP:0008872HP:0008872Feeding difficulties in infancy1ARID1B CL E G H574921465ORPHA118857518040614556
HP:0008872HP:0008872Feeding difficulties in infancy1ARID1B CL E G H57492135900Coffin-Siris syndrome 1135900C3281201OMIM118857518040614556
HP:0008872HP:0008872Feeding difficulties in infancy1ARID2 CL E G H1965281465ORPHA11111518037609539
HP:0008872HP:0008872Feeding difficulties in infancy1ARL13B CL E G H200894475Acquired hypoprothrombinemiaORPHA11012025419608922
HP:0008872HP:0008872Feeding difficulties in infancy1ARL3 CL E G H403475Acquired hypoprothrombinemiaORPHA1333694604695
HP:0008872HP:0008872Feeding difficulties in infancy1ARMC9 CL E G H80210475Acquired hypoprothrombinemiaORPHA11110520730617612
HP:0008872HP:0008872Feeding difficulties in infancy1ARX CL E G H170302300215Lissencephaly 2, X-linked300215C1846171OMIM19846618060300382
HP:0008872HP:0008872Feeding difficulties in infancy1ASL CL E G H435207900Argininosuccinate lyase deficiency207900C0268547OMIM1169264746608310
HP:0008872HP:0008872Feeding difficulties in infancy1ASXL2 CL E G H55252617190Shashi-Pena syndrome617190C4310672OMIM168123805612991
HP:0008872HP:0008872Feeding difficulties in infancy1ATP6V0A2 CL E G H23545219200Cutis laxa with osteodystrophy219200C0268355OMIM15630918481611716
HP:0008872HP:0008872Feeding difficulties in infancy1ATP7A CL E G H538565ORPHA1357607869300011
HP:0008872HP:0008872Feeding difficulties in infancy1AVPR2 CL E G H554304800Nephrogenic diabetes insipidus, X-linked304800C1563705OMIM1286356897300538
HP:0008872HP:0008872Feeding difficulties in infancy1B3GLCT CL E G H145173709ORPHA11518120207610308
HP:0008872HP:0008872Feeding difficulties in infancy1B3GLCT CL E G H145173261540Peters plus syndrome261540C0796012OMIM11518120207610308
HP:0008872HP:0008872Feeding difficulties in infancy1B9D1 CL E G H27077475Acquired hypoprothrombinemiaORPHA11015824123614144
HP:0008872HP:0008872Feeding difficulties in infancy1BCKDHA CL E G H593248600Maple syrup urine disease248600C0024776OMIM1101255986608348
HP:0008872HP:0008872Feeding difficulties in infancy1BCKDHB CL E G H594248600Maple syrup urine disease248600C0024776OMIM1115319987248611
HP:0008872HP:0008872Feeding difficulties in infancy1BCS1L CL E G H617124000Mitochondrial complex III deficiency124000C1852372OMIM1371741020603647
HP:0008872HP:0008872Feeding difficulties in infancy1BIN1 CL E G H274255200Autosomal recessive centronuclear myopathy255200C0410204OMIM1173151052601248
HP:0008872HP:0008872Feeding difficulties in infancy1BRAF CL E G H673648ORPHA1684901097164757
HP:0008872HP:0008872Feeding difficulties in infancy1BRAF CL E G H673115150Cardiofaciocutaneous syndrome 1115150CN029449OMIM1684901097164757
HP:0008872HP:0008872Feeding difficulties in infancy1BRAF CL E G H6731340Chromosome 4, monosomy 4qC0265404ORPHA1684901097164757
HP:0008872HP:0008872Feeding difficulties in infancy1BTD CL E G H686253260Biotinidase deficiency253260C0220754OMIM12483711122609019
HP:0008872HP:0008872Feeding difficulties in infancy1BUB1B CL E G H701257300Mosaic variegated aneuploidy syndrome 1257300CN031748OMIM1293231149602860
HP:0008872HP:0008872Feeding difficulties in infancy1CASR CL E G H846239200Neonatal severe hyperparathyroidism239200C1832615OMIM14109551514601199
HP:0008872HP:0008872Feeding difficulties in infancy1CC2D2A CL E G H575451454Common atrioventricular canalC0221215ORPHA19658429253612013
HP:0008872HP:0008872Feeding difficulties in infancy1CEP104 CL E G H9731475Acquired hypoprothrombinemiaORPHA1715224866616690
HP:0008872HP:0008872Feeding difficulties in infancy1CEP120 CL E G H153241475Acquired hypoprothrombinemiaORPHA198726690613446
HP:0008872HP:0008872Feeding difficulties in infancy1CEP41 CL E G H95681475Acquired hypoprothrombinemiaORPHA11123212370610523
HP:0008872HP:0008872Feeding difficulties in infancy1CHD7 CL E G H55636138ORPHA1884126620626608892
HP:0008872HP:0008872Feeding difficulties in infancy1CHRNE CL E G H1145605809Myasthenic syndrome, congenital, 4a, slow-channel605809C1853949OMIM11383871966100725
HP:0008872HP:0008872Feeding difficulties in infancy1CISD2 CL E G H4938563463ORPHA142324212611507
HP:0008872HP:0008872Feeding difficulties in infancy1CLCF1 CL E G H23529610313Cold-induced sweating syndrome 2610313C1853198OMIM142517412607672
HP:0008872HP:0008872Feeding difficulties in infancy1CLDN16 CL E G H10686248250Primary hypomagnesemia248250C0268448OMIM1651882037603959
HP:0008872HP:0008872Feeding difficulties in infancy1COL11A2 CL E G H13021427ORPHA1594712187120290
HP:0008872HP:0008872Feeding difficulties in infancy1COL6A1 CL E G H1291254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM113710072211120220
HP:0008872HP:0008872Feeding difficulties in infancy1COL6A2 CL E G H1292254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM119111482212120240
HP:0008872HP:0008872Feeding difficulties in infancy1COL6A3 CL E G H1293254090Ullrich congenital muscular dystrophy 1254090CN033863OMIM114316342213120250
HP:0008872HP:0008872Feeding difficulties in infancy1COLQ CL E G H8292603034Endplate acetylcholinesterase deficiency603034C1864233OMIM1702622226603033
HP:0008872HP:0008872Feeding difficulties in infancy1CPLANE1 CL E G H652502754ORPHA111859425801614571
HP:0008872HP:0008872Feeding difficulties in infancy1CPLANE1 CL E G H65250475Acquired hypoprothrombinemiaORPHA111859425801614571
HP:0008872HP:0008872Feeding difficulties in infancy1CPT1A CL E G H1374255120Carnitine palmitoyltransferase I deficiency255120C0342789OMIM1532392328600528
HP:0008872HP:0008872Feeding difficulties in infancy1CPT2 CL E G H1376608836Carnitine palmitoyltransferase II deficiency, lethal neonatal608836C1833518OMIM11133662330600650
HP:0008872HP:0008872Feeding difficulties in infancy1CREBBP CL E G H1387180849Rubinstein-Taybi syndrome180849C0035934OMIM13647552348600140
HP:0008872HP:0008872Feeding difficulties in infancy1CRLF1 CL E G H9244272430Cold-induced sweating syndrome 1272430C1848947OMIM137562364604237
HP:0008872HP:0008872Feeding difficulties in infancy1CSPP1 CL E G H79848475Acquired hypoprothrombinemiaORPHA12725726193611654
HP:0008872HP:0008872Feeding difficulties in infancy1CYP11B2 CL E G H1585203400Corticosterone methyloxidase type 1 deficiency203400CN074214OMIM1552212592124080
HP:0008872HP:0008872Feeding difficulties in infancy1DBT CL E G H1629248600Maple syrup urine disease248600C0024776OMIM1783402698248610
HP:0008872HP:0008872Feeding difficulties in infancy1DDC CL E G H1644608643Deficiency of aromatic-L-amino-acid decarboxylase608643C1291564OMIM1591162719107930
HP:0008872HP:0008872Feeding difficulties in infancy1DEAF1 CL E G H10522819ORPHA11712914677602635
HP:0008872HP:0008872Feeding difficulties in infancy1DGUOK CL E G H1716251880Mitochondrial DNA-depletion syndrome 3, hepatocerebral251880C3151513OMIM1641222858601465
HP:0008872HP:0008872Feeding difficulties in infancy1DHCR7 CL E G H1717818ORPHA12183762860602858
HP:0008872HP:0008872Feeding difficulties in infancy1DLEC1 CL E G H994099977ORPHA13382899604050
HP:0008872HP:0008872Feeding difficulties in infancy1DMPK CL E G H1760160900Steinert myotonic dystrophy syndrome160900C3250443OMIM182332933605377
HP:0008872HP:0008872Feeding difficulties in infancy1DPF2 CL E G H59771465ORPHA19149964601671
HP:0008872HP:0008872Feeding difficulties in infancy1DPYS CL E G H1807222748Dihydropyrimidinase deficiency222748C0342803OMIM1301083013613326
HP:0008872HP:0008872Feeding difficulties in infancy1EED CL E G H87263447ORPHA19493188605984
HP:0008872HP:0008872Feeding difficulties in infancy1EFTUD2 CL E G H9343610536Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate610536C1864652OMIM110112430858603892
HP:0008872HP:0008872Feeding difficulties in infancy1ELN CL E G H2006194050Williams syndrome194050C0175702OMIM11275233327130160
HP:0008872HP:0008872Feeding difficulties in infancy1ELP1 CL E G H85181764ORPHA166605959603722
HP:0008872HP:0008872Feeding difficulties in infancy1ELP1 CL E G H8518223900Familial dysautonomia223900C0013364OMIM166605959603722
HP:0008872HP:0008872Feeding difficulties in infancy1EMG1 CL E G H104361270ORPHA115916912611531
HP:0008872HP:0008872Feeding difficulties in infancy1EP300 CL E G H2033180849Rubinstein-Taybi syndrome180849C0035934OMIM11074153373602700
HP:0008872HP:0008872Feeding difficulties in infancy1ERCC1 CL E G H20671466ORPHA18533433126380
HP:0008872HP:0008872Feeding difficulties in infancy1ERCC2 CL E G H20681466ORPHA11082273434126340
HP:0008872HP:0008872Feeding difficulties in infancy1ERCC5 CL E G H20731466ORPHA1592633437133530
HP:0008872HP:0008872Feeding difficulties in infancy1ERCC6 CL E G H20741466ORPHA11404993438609413
HP:0008872HP:0008872Feeding difficulties in infancy1EZH2 CL E G H21463447ORPHA1422353527601573
HP:0008872HP:0008872Feeding difficulties in infancy1FGFR2 CL E G H226387ORPHA11593363689176943
HP:0008872HP:0008872Feeding difficulties in infancy1FKRP CL E G H79147606612Congenital muscular dystrophy-dystroglycanopathy (with or without mental retardation) type B5606612C1847759OMIM114140217997606596
HP:0008872HP:0008872Feeding difficulties in infancy1FLCN CL E G H201163610883Chromosome 17, trisomy 17p11 2610883C2931246OMIM1215103627310607273
HP:0008872HP:0008872Feeding difficulties in infancy1FLI1 CL E G H23132308Fetal minoxidil syndromeORPHA171253749193067
HP:0008872HP:0008872Feeding difficulties in infancy1FLII CL E G H2314819ORPHA121533750600362
HP:0008872HP:0008872Feeding difficulties in infancy1FLNA CL E G H2316300048Intestinal pseudoobstruction neuronal chronic idiopathic X-linked300048C2746068OMIM127114723754300017
HP:0008872HP:0008872Feeding difficulties in infancy1GABRD CL E G H25631606ORPHA172784084137163
HP:0008872HP:0008872Feeding difficulties in infancy1GCDH CL E G H263925ORPHA12443374189608801
HP:0008872HP:0008872Feeding difficulties in infancy1HADH CL E G H3033231530Deficiency of 3-hydroxyacyl-CoA dehydrogenase231530C1291230OMIM126944799601609
HP:0008872HP:0008872Feeding difficulties in infancy1HDAC8 CL E G H55869199Cardiac hydatid cysts with intracavitary expansionORPHA15622713315300269
HP:0008872HP:0008872Feeding difficulties in infancy1HLCS CL E G H3141253270Holocarboxylase synthetase deficiency253270C0268581OMIM1493734976609018
HP:0008872HP:0008872Feeding difficulties in infancy1HSD17B4 CL E G H3295261515Bifunctional peroxisomal enzyme deficiency261515C0342870OMIM11013055213601860
HP:0008872HP:0008872Feeding difficulties in infancy1HSPD1 CL E G H3329612233Leukodystrophy, hypomyelinating, 4612233C2677109OMIM161285261118190
HP:0008872HP:0008872Feeding difficulties in infancy1HYLS1 CL E G H219844475Acquired hypoprothrombinemiaORPHA1212226558610693
HP:0008872HP:0008872Feeding difficulties in infancy1IGF2 CL E G H3481616489Growth restriction, severe, with distinctive facies616489C4225307OMIM111675466147470
HP:0008872HP:0008872Feeding difficulties in infancy1INPP5E CL E G H56623475Acquired hypoprothrombinemiaORPHA15432521474613037
HP:0008872HP:0008872Feeding difficulties in infancy1INPP5E CL E G H566231454Common atrioventricular canalC0221215ORPHA15432521474613037
HP:0008872HP:0008872Feeding difficulties in infancy1INSR CL E G H3643508Acroosteolysis dominant typeORPHA11964076091147670
HP:0008872HP:0008872Feeding difficulties in infancy1IQSEC2 CL E G H23096819ORPHA15753929059300522
HP:0008872HP:0008872Feeding difficulties in infancy1KANSL1 CL E G H284058610443Koolen-de Vries syndrome610443C1864871OMIM17284024565612452
HP:0008872HP:0008872Feeding difficulties in infancy1KAT6B CL E G H23522648ORPHA17622817582605880
HP:0008872HP:0008872Feeding difficulties in infancy1KCNAB2 CL E G H85141606ORPHA15856229601142
HP:0008872HP:0008872Feeding difficulties in infancy1KCNK9 CL E G H51305612292Birk Barel mental retardation dysmorphism syndrome612292C2676770OMIM12656283605874
HP:0008872HP:0008872Feeding difficulties in infancy1KDM6A CL E G H7403147920Kabuki syndrome 1147920CN030661OMIM18131112637300128
HP:0008872HP:0008872Feeding difficulties in infancy1KDM6A CL E G H7403300867Kabuki syndrome 2300867C3275495OMIM18131112637300128
HP:0008872HP:0008872Feeding difficulties in infancy1KIAA0556 CL E G H23247475Acquired hypoprothrombinemiaORPHA1229068616650
HP:0008872HP:0008872Feeding difficulties in infancy1KIAA0586 CL E G H9786475Acquired hypoprothrombinemiaORPHA13115519960610178
HP:0008872HP:0008872Feeding difficulties in infancy1KIAA0753 CL E G H98512754ORPHA176529110617112
HP:0008872HP:0008872Feeding difficulties in infancy1KIF1A CL E G H547201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1431059888601255
HP:0008872HP:0008872Feeding difficulties in infancy1KIF7 CL E G H3746542754ORPHA14538630497611254
HP:0008872HP:0008872Feeding difficulties in infancy1KMT2A CL E G H4297199Cardiac hydatid cysts with intracavitary expansionORPHA11273797132159555
HP:0008872HP:0008872Feeding difficulties in infancy1KMT2D CL E G H8085147920Kabuki syndrome 1147920CN030661OMIM171213507133602113
HP:0008872HP:0008872Feeding difficulties in infancy1KRAS CL E G H3845648ORPHA1452746407190070
HP:0008872HP:0008872Feeding difficulties in infancy1KRAS CL E G H38451340Chromosome 4, monosomy 4qC0265404ORPHA1452746407190070
HP:0008872HP:0008872Feeding difficulties in infancy1LAMA2 CL E G H3908607855Merosin deficient congenital muscular dystrophy607855C1263858OMIM138014996482156225
HP:0008872HP:0008872Feeding difficulties in infancy1LIFR CL E G H39773206ORPHA1323466597151443
HP:0008872HP:0008872Feeding difficulties in infancy1LMBRD1 CL E G H5578879284ORPHA1910423038612625
HP:0008872HP:0008872Feeding difficulties in infancy1LMBRD1 CL E G H55788277380METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE277380C1848578OMIM1910423038612625
HP:0008872HP:0008872Feeding difficulties in infancy1LZTR1 CL E G H8216648ORPHA1866996742600574
HP:0008872HP:0008872Feeding difficulties in infancy1MAP2K1 CL E G H56041340Chromosome 4, monosomy 4qC0265404ORPHA1232136840176872
HP:0008872HP:0008872Feeding difficulties in infancy1MAP2K2 CL E G H56051340Chromosome 4, monosomy 4qC0265404ORPHA1353386842601263
HP:0008872HP:0008872Feeding difficulties in infancy1MBD5 CL E G H55777156200Mental retardation, autosomal dominant 1156200C1969562OMIM19166420444611472
HP:0008872HP:0008872Feeding difficulties in infancy1MCCC1 CL E G H569222102003 Methylcrotonyl-CoA carboxylase 1 deficiency210200CN028786OMIM11082736936609010
HP:0008872HP:0008872Feeding difficulties in infancy1MECP2 CL E G H4204300673Severe neonatal-onset encephalopathy with microcephaly300673C1968556OMIM1105014426990300005
HP:0008872HP:0008872Feeding difficulties in infancy1MKS1 CL E G H54903475Acquired hypoprothrombinemiaORPHA1523347121609883
HP:0008872HP:0008872Feeding difficulties in infancy1MLXIPL CL E G H51085194050Williams syndrome194050C0175702OMIM1619712744605678
HP:0008872HP:0008872Feeding difficulties in infancy1MMAA CL E G H166785251100Methylmalonic aciduria cblA type251100C1855109OMIM17626318871607481
HP:0008872HP:0008872Feeding difficulties in infancy1MMAB CL E G H326625251110Methylmalonic aciduria cblB type251110C1855102OMIM14225619331607568
HP:0008872HP:0008872Feeding difficulties in infancy1MMACHC CL E G H25974277400Methylmalonic acidemia with homocystinuria277400C1848561OMIM19527424525609831
HP:0008872HP:0008872Feeding difficulties in infancy1MOCS1 CL E G H4337252150Molybdenum cofactor deficiency, complementation group A252150C1854988OMIM1351817190603707
HP:0008872HP:0008872Feeding difficulties in infancy1MOGS CL E G H7841606056Congenital disorder of glycosylation type 2B606056C1853736OMIM1817324862601336
HP:0008872HP:0008872Feeding difficulties in infancy1MRPS16 CL E G H51021610498Combined oxidative phosphorylation deficiency 2610498C1864843OMIM115114048609204
HP:0008872HP:0008872Feeding difficulties in infancy1MTR CL E G H4548250940METHYLCOBALAMIN DEFICIENCY, cblG TYPE250940C1855128OMIM1444287468156570
HP:0008872HP:0008872Feeding difficulties in infancy1MYH3 CL E G H46212053Ectodermal dysplasia neurosensory deafnessORPHA1453157573160720
HP:0008872HP:0008872Feeding difficulties in infancy1MYH3 CL E G H4621193700Freeman-Sheldon syndrome193700C0265224OMIM1453157573160720
HP:0008872HP:0008872Feeding difficulties in infancy1NALCN CL E G H2592322053Ectodermal dysplasia neurosensory deafnessORPHA16524719082611549
HP:0008872HP:0008872Feeding difficulties in infancy1NDUFS4 CL E G H4724252010Mitochondrial complex I deficiency252010C1838979OMIM117697711602694
HP:0008872HP:0008872Feeding difficulties in infancy1NIPBL CL E G H25836199Cardiac hydatid cysts with intracavitary expansionORPHA143780928862608667
HP:0008872HP:0008872Feeding difficulties in infancy1NRAS CL E G H4893648ORPHA1141817989164790
HP:0008872HP:0008872Feeding difficulties in infancy1NSD1 CL E G H643243447ORPHA152589614234606681
HP:0008872HP:0008872Feeding difficulties in infancy1NSD1 CL E G H64324821ORPHA152589614234606681
HP:0008872HP:0008872Feeding difficulties in infancy1OCRL CL E G H4952534Acute myeloblastic leukemia without maturationORPHA12643428108300535
HP:0008872HP:0008872Feeding difficulties in infancy1OFD1 CL E G H84812754ORPHA11625102567300170
HP:0008872HP:0008872Feeding difficulties in infancy1OFD1 CL E G H8481300804Joubert syndrome 10300804C2749019OMIM11625102567300170
HP:0008872HP:0008872Feeding difficulties in infancy1OPA1 CL E G H4976616896Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)616896C4225163OMIM13944418140605290
HP:0008872HP:0008872Feeding difficulties in infancy1ORC1 CL E G H4998224690Meier-Gorlin syndrome 1224690CN030358OMIM1121038487601902
HP:0008872HP:0008872Feeding difficulties in infancy1PANK2 CL E G H80025234200Pigmentary pallidal degeneration234200C0018523OMIM118219215894606157
HP:0008872HP:0008872Feeding difficulties in infancy1PAX8 CL E G H7849218700Thyroid dysgenesis218700C1563716OMIM1511438622167415
HP:0008872HP:0008872Feeding difficulties in infancy1PCCA CL E G H5095606054Propionyl-CoA carboxylase deficiency606054C0268579OMIM11493878653232000
HP:0008872HP:0008872Feeding difficulties in infancy1PCCB CL E G H5096606054Propionyl-CoA carboxylase deficiency606054C0268579OMIM11313018654232050
HP:0008872HP:0008872Feeding difficulties in infancy1PDE6D CL E G H51472754ORPHA11398788602676
HP:0008872HP:0008872Feeding difficulties in infancy1PEX1 CL E G H5189912ORPHA11404898850602136
HP:0008872HP:0008872Feeding difficulties in infancy1PEX10 CL E G H5192912ORPHA1323478851602859
HP:0008872HP:0008872Feeding difficulties in infancy1PEX10 CL E G H5192614870Peroxisome biogenesis disorder 6A614870C3553947OMIM1323478851602859
HP:0008872HP:0008872Feeding difficulties in infancy1PEX11B CL E G H8799912ORPHA182478853603867
HP:0008872HP:0008872Feeding difficulties in infancy1PEX12 CL E G H5193912ORPHA1371818854601758
HP:0008872HP:0008872Feeding difficulties in infancy1PEX12 CL E G H5193614859Peroxisome biogenesis disorder 3A614859C3553929OMIM1371818854601758
HP:0008872HP:0008872Feeding difficulties in infancy1PEX13 CL E G H5194912ORPHA1101968855601789
HP:0008872HP:0008872Feeding difficulties in infancy1PEX14 CL E G H5195912ORPHA151768856601791
HP:0008872HP:0008872Feeding difficulties in infancy1PEX16 CL E G H9409912ORPHA1151498857603360
HP:0008872HP:0008872Feeding difficulties in infancy1PEX16 CL E G H9409614876Peroxisome biogenesis disorder 8A614876C3553959OMIM1151498857603360
HP:0008872HP:0008872Feeding difficulties in infancy1PEX19 CL E G H5824912ORPHA141339713600279
HP:0008872HP:0008872Feeding difficulties in infancy1PEX2 CL E G H5828912ORPHA1182089717170993
HP:0008872HP:0008872Feeding difficulties in infancy1PEX26 CL E G H55670912ORPHA12727722965608666
HP:0008872HP:0008872Feeding difficulties in infancy1PEX3 CL E G H8504912ORPHA1101168858603164
HP:0008872HP:0008872Feeding difficulties in infancy1PEX5 CL E G H5830912ORPHA1142809719600414
HP:0008872HP:0008872Feeding difficulties in infancy1PEX6 CL E G H5190912ORPHA11093758859601498
HP:0008872HP:0008872Feeding difficulties in infancy1PEX6 CL E G H5190614862Peroxisome biogenesis disorder 4a (zellweger)614862C3553936OMIM11093758859601498
HP:0008872HP:0008872Feeding difficulties in infancy1PHF6 CL E G H84295127ORPHA12923518145300414
HP:0008872HP:0008872Feeding difficulties in infancy1PIBF1 CL E G H10464475Acquired hypoprothrombinemiaORPHA188723352607532
HP:0008872HP:0008872Feeding difficulties in infancy1PIGN CL E G H23556280633Multiple congenital anomalies-hypotonia-seizures syndromeCN228166ORPHA1344168967606097
HP:0008872HP:0008872Feeding difficulties in infancy1PLXND1 CL E G H23129570ORPHA181049107604282
HP:0008872HP:0008872Feeding difficulties in infancy1PMM2 CL E G H5373212065Carbohydrate-deficient glycoprotein syndrome type I212065C0349653OMIM11293639115601785
HP:0008872HP:0008872Feeding difficulties in infancy1PNPO CL E G H55163610090Pyridoxal 5'-phosphate-dependent epilepsy610090C1864723OMIM13118430260603287
HP:0008872HP:0008872Feeding difficulties in infancy1PRDM16 CL E G H639761606ORPHA12167714000605557
HP:0008872HP:0008872Feeding difficulties in infancy1PRDX1 CL E G H5052277400Methylmalonic acidemia with homocystinuria277400C1848561OMIM13229352176763
HP:0008872HP:0008872Feeding difficulties in infancy1PSAT1 CL E G H29968610992Phosphoserine aminotransferase deficiency610992C1970253OMIM11032319129610936
HP:0008872HP:0008872Feeding difficulties in infancy1PTPN11 CL E G H5781648ORPHA11434759644176876
HP:0008872HP:0008872Feeding difficulties in infancy1RAB3GAP1 CL E G H229301387Cleft palate cardiac defect ectrodactylyORPHA16719317063602536
HP:0008872HP:0008872Feeding difficulties in infancy1RAB3GAP2 CL E G H257821387Cleft palate cardiac defect ectrodactylyORPHA11629417168609275
HP:0008872HP:0008872Feeding difficulties in infancy1RAB3GAP2 CL E G H25782212720Martsolf syndrome212720C0796037OMIM11629417168609275
HP:0008872HP:0008872Feeding difficulties in infancy1RAD21 CL E G H5885199Cardiac hydatid cysts with intracavitary expansionORPHA1131499811606462
HP:0008872HP:0008872Feeding difficulties in infancy1RAF1 CL E G H5894648ORPHA1545089829164760
HP:0008872HP:0008872Feeding difficulties in infancy1RAI1 CL E G H10743819ORPHA11164049834607642
HP:0008872HP:0008872Feeding difficulties in infancy1RASA2 CL E G H5922648ORPHA13739872601589
HP:0008872HP:0008872Feeding difficulties in infancy1RERE CL E G H4731606ORPHA1251619965605226
HP:0008872HP:0008872Feeding difficulties in infancy1RETREG1 CL E G H54463201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1628925964613114
HP:0008872HP:0008872Feeding difficulties in infancy1REV3L CL E G H5980570ORPHA191249968602776
HP:0008872HP:0008872Feeding difficulties in infancy1RIT1 CL E G H6016648ORPHA12610610023609591
HP:0008872HP:0008872Feeding difficulties in infancy1RNF6 CL E G H604999977ORPHA113710069604242
HP:0008872HP:0008872Feeding difficulties in infancy1RPGRIP1L CL E G H233221454Common atrioventricular canalC0221215ORPHA15143229168610937
HP:0008872HP:0008872Feeding difficulties in infancy1RPS6KA3 CL E G H6197192Karandikar Maria Kamble syndromeORPHA117130910432300075
HP:0008872HP:0008872Feeding difficulties in infancy1RRAS CL E G H6237648ORPHA127510447165090
HP:0008872HP:0008872Feeding difficulties in infancy1RYR1 CL E G H6261255320Minicore myopathy255320C1850674OMIM1688309410483180901
HP:0008872HP:0008872Feeding difficulties in infancy1SAMHD1 CL E G H25939612952Aicardi Goutieres syndrome 5612952C2749659OMIM15720015925606754
HP:0008872HP:0008872Feeding difficulties in infancy1SCN9A CL E G H6335201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1129109210597603415
HP:0008872HP:0008872Feeding difficulties in infancy1SCNN1A CL E G H6337264350Pseudohypoaldosteronism type 1 autosomal recessive264350C1449843OMIM14917110599600228
HP:0008872HP:0008872Feeding difficulties in infancy1SCNN1B CL E G H6338264350Pseudohypoaldosteronism type 1 autosomal recessive264350C1449843OMIM15014510600600760
HP:0008872HP:0008872Feeding difficulties in infancy1SCNN1G CL E G H6340264350Pseudohypoaldosteronism type 1 autosomal recessive264350C1449843OMIM12312110602600761
HP:0008872HP:0008872Feeding difficulties in infancy1SCO2 CL E G H9997604377Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency604377C1858424OMIM13727510604604272
HP:0008872HP:0008872Feeding difficulties in infancy1SEMA3E CL E G H9723138ORPHA1416010727608166
HP:0008872HP:0008872Feeding difficulties in infancy1SETD2 CL E G H29072821ORPHA11943318420612778
HP:0008872HP:0008872Feeding difficulties in infancy1SETD5 CL E G H55209199Cardiac hydatid cysts with intracavitary expansionORPHA13823625566615743
HP:0008872HP:0008872Feeding difficulties in infancy1SIN3A CL E G H25942613406Witteveen-kolk syndrome613406C3150674OMIM11611619353607776
HP:0008872HP:0008872Feeding difficulties in infancy1SKI CL E G H64971606ORPHA12450210896164780
HP:0008872HP:0008872Feeding difficulties in infancy1SLC16A2 CL E G H6567300523Allan-Herndon-Dudley syndrome300523C0795889OMIM18825710923300095
HP:0008872HP:0008872Feeding difficulties in infancy1SLC46A1 CL E G H113235229050Congenital defect of folate absorption229050C0342705OMIM12316630521611672
HP:0008872HP:0008872Feeding difficulties in infancy1SLC6A8 CL E G H6535300352Creatine deficiency, X-linked300352C1845862OMIM113954211055300036
HP:0008872HP:0008872Feeding difficulties in infancy1SLC9A6 CL E G H1047985278ORPHA12835111079300231
HP:0008872HP:0008872Feeding difficulties in infancy1SMARCA4 CL E G H65971465ORPHA157247311100603254
HP:0008872HP:0008872Feeding difficulties in infancy1SMARCB1 CL E G H65981465ORPHA111948211103601607
HP:0008872HP:0008872Feeding difficulties in infancy1SMARCE1 CL E G H66051465ORPHA11328711109603111
HP:0008872HP:0008872Feeding difficulties in infancy1SMC1A CL E G H8243199Cardiac hydatid cysts with intracavitary expansionORPHA110048411111300040
HP:0008872HP:0008872Feeding difficulties in infancy1SMC3 CL E G H9126199Cardiac hydatid cysts with intracavitary expansionORPHA1282132468606062
HP:0008872HP:0008872Feeding difficulties in infancy1SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM1282132468606062
HP:0008872HP:0008872Feeding difficulties in infancy1SMPD1 CL E G H6609257200Niemann-Pick disease, type A257200C0268242OMIM125439711120607608
HP:0008872HP:0008872Feeding difficulties in infancy1SOS1 CL E G H6654648ORPHA17566511187182530
HP:0008872HP:0008872Feeding difficulties in infancy1SOS2 CL E G H6655648ORPHA1632411188601247
HP:0008872HP:0008872Feeding difficulties in infancy1SOX11 CL E G H66641465ORPHA1147011191600898
HP:0008872HP:0008872Feeding difficulties in infancy1SRCAP CL E G H108472044Ectodermal dysplasia Berlin typeORPHA14424516974611421
HP:0008872HP:0008872Feeding difficulties in infancy1ST3GAL5 CL E G H8869609056Amish infantile epilepsy syndrome609056C1836824OMIM1716310872604402
HP:0008872HP:0008872Feeding difficulties in infancy1SUCLA2 CL E G H8803612073Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)612073C2749864OMIM12918911448603921
HP:0008872HP:0008872Feeding difficulties in infancy1SUZ12 CL E G H235123447ORPHA137217101606245
HP:0008872HP:0008872Feeding difficulties in infancy1TCTN1 CL E G H79600475Acquired hypoprothrombinemiaORPHA1611626113609863
HP:0008872HP:0008872Feeding difficulties in infancy1TCTN2 CL E G H79867475Acquired hypoprothrombinemiaORPHA11520325774613846
HP:0008872HP:0008872Feeding difficulties in infancy1TCTN3 CL E G H261232754ORPHA1129524519613847
HP:0008872HP:0008872Feeding difficulties in infancy1TGFBR2 CL E G H704899977ORPHA114857211773190182
HP:0008872HP:0008872Feeding difficulties in infancy1TK2 CL E G H7084254875ORPHA16020611831188250
HP:0008872HP:0008872Feeding difficulties in infancy1TMEM216 CL E G H512592754ORPHA1810925018613277
HP:0008872HP:0008872Feeding difficulties in infancy1TMEM237 CL E G H65062475Acquired hypoprothrombinemiaORPHA11122114432614423
HP:0008872HP:0008872Feeding difficulties in infancy1TMEM67 CL E G H91147475Acquired hypoprothrombinemiaORPHA117431628396609884
HP:0008872HP:0008872Feeding difficulties in infancy1TMEM67 CL E G H911471454Common atrioventricular canalC0221215ORPHA117431628396609884
HP:0008872HP:0008872Feeding difficulties in infancy1TPM2 CL E G H7169609285Nemaline myopathy 4609285C1836447OMIM14019912011190990
HP:0008872HP:0008872Feeding difficulties in infancy1TREX1 CL E G H11277225750Aicardi Goutieres syndrome 1225750C0796126OMIM17115312269606609
HP:0008872HP:0008872Feeding difficulties in infancy1TRMU CL E G H55687613070Liver failure acute infantile613070C3278664OMIM12329625481610230
HP:0008872HP:0008872Feeding difficulties in infancy1TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM12117627561608755
HP:0008872HP:0008872Feeding difficulties in infancy1TSFM CL E G H10102610505Combined oxidative phosphorylation deficiency 3610505C1864840OMIM1710312367604723
HP:0008872HP:0008872Feeding difficulties in infancy1TSPYL1 CL E G H7259608800Sudden infant death with dysgenesis of the testes syndrome608800C1837371OMIM183212382604714
HP:0008872HP:0008872Feeding difficulties in infancy1TUBB3 CL E G H10381300570ORPHA12615520772602661
HP:0008872HP:0008872Feeding difficulties in infancy1TXNL4A CL E G H10907608572Burn-McKeown syndrome608572C1837822OMIM11317630551611595
HP:0008872HP:0008872Feeding difficulties in infancy1UBE3A CL E G H7337105830Angelman syndrome105830C0162635OMIM120275912496601623
HP:0008872HP:0008872Feeding difficulties in infancy1VPS13B CL E G H157680193ORPHA121316062183607817
HP:0008872HP:0008872Feeding difficulties in infancy1VPS13B CL E G H157680216550Cohen syndrome216550C0265223OMIM121316062183607817
HP:0008872HP:0008872Feeding difficulties in infancy1VRK1 CL E G H7443607596Pontocerebellar hypoplasia type 1A607596CN032785OMIM11018612718602168
HP:0008872HP:0008872Feeding difficulties in infancy1WFS1 CL E G H74663463ORPHA139371412762606201
HP:0008872HP:0008872Feeding difficulties in infancy1WNK1 CL E G H65125201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM11882014540605232
HP:0008872HP:0008872Feeding difficulties in infancy1WWOX CL E G H5174199977ORPHA15059612799605131
HP:0008872HP:0008872Feeding difficulties in infancy1ZNHIT3 CL E G H9326260565PEHO syndrome260565C1850055OMIM119912309604500
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008872HP:0008872Feeding difficulties in infancy0AIFM1 CL E G H9131238329ORPHA0333438768300169
HP:0008872HP:0008872Feeding difficulties in infancy0ARSA CL E G H410309256ORPHA0254567713607574
HP:0008872HP:0008872Feeding difficulties in infancy0ARVCF CL E G H421567ORPHA02477728602269
HP:0008872HP:0008872Feeding difficulties in infancy0ATRX CL E G H546847ORPHA0170663886300032
HP:0008872HP:0008872Feeding difficulties in infancy0BCOR CL E G H548802712HMG CoA synthetase deficiencyCN072869ORPHA05541520893300485
HP:0008872HP:0008872Feeding difficulties in infancy0CASK CL E G H8573300422FG syndrome 4300422CN033933OMIM01194461497300172
HP:0008872HP:0008872Feeding difficulties in infancy0CCDC22 CL E G H289527Typical Joubert syndrome MRI findingsCN228298ORPHA0722128909300859
HP:0008872HP:0008872Feeding difficulties in infancy0CEP120 CL E G H153241474ORPHA098726690613446
HP:0008872HP:0008872Feeding difficulties in infancy0CLEC7A CL E G H645811334ORPHA014514558606264
HP:0008872HP:0008872Feeding difficulties in infancy0COL1A1 CL E G H12771310ORPHA096711052197120150
HP:0008872HP:0008872Feeding difficulties in infancy0COMT CL E G H1312567ORPHA0155552228116790
HP:0008872HP:0008872Feeding difficulties in infancy0DYNC2H1 CL E G H79659474ORPHA02078892962603297
HP:0008872HP:0008872Feeding difficulties in infancy0DYNC2LI1 CL E G H51626474ORPHA01417324595617083
HP:0008872HP:0008872Feeding difficulties in infancy0DYRK1A CL E G H1859614104Mental retardation, autosomal dominant 7614104C3279839OMIM0774373091600855
HP:0008872HP:0008872Feeding difficulties in infancy0EPG5 CL E G H577241493Congenital mesoblastic nephromaORPHA06849529331615068
HP:0008872HP:0008872Feeding difficulties in infancy0GP1BB CL E G H2812567ORPHA0534044440138720
HP:0008872HP:0008872Feeding difficulties in infancy0HADH CL E G H303371212ORPHA026944799601609
HP:0008872HP:0008872Feeding difficulties in infancy0HDAC8 CL E G H55869300882Cornelia de Lange syndrome 5300882C3550903OMIM05622713315300269
HP:0008872HP:0008872Feeding difficulties in infancy0HIRA CL E G H7290567ORPHA053994916600237
HP:0008872HP:0008872Feeding difficulties in infancy0HSPG2 CL E G H3339800ORPHA0678625273142461
HP:0008872HP:0008872Feeding difficulties in infancy0IFT140 CL E G H9742474ORPHA07253029077614620
HP:0008872HP:0008872Feeding difficulties in infancy0IFT172 CL E G H26160474ORPHA02726930391607386
HP:0008872HP:0008872Feeding difficulties in infancy0IFT80 CL E G H57560474ORPHA01321129262611177
HP:0008872HP:0008872Feeding difficulties in infancy0IL17F CL E G H1127441334ORPHA056016404606496
HP:0008872HP:0008872Feeding difficulties in infancy0IL17RA CL E G H237651334ORPHA0195005985605461
HP:0008872HP:0008872Feeding difficulties in infancy0IL17RC CL E G H848181334ORPHA0421718358610925
HP:0008872HP:0008872Feeding difficulties in infancy0JMJD1C CL E G H221037567ORPHA02950912313604503
HP:0008872HP:0008872Feeding difficulties in infancy0LRP5 CL E G H40412924Hypoplastic thumbs hydranencephalyORPHA02214116697603506
HP:0008872HP:0008872Feeding difficulties in infancy0MAP3K7 CL E G H6885617137Frontometaphyseal dysplasia 2617137C4310697OMIM013646859602614
HP:0008872HP:0008872Feeding difficulties in infancy0MT-CO1 CL E G H4512550ORPHA07419516030
HP:0008872HP:0008872Feeding difficulties in infancy0MT-CO2 CL E G H4513550ORPHA07421516040
HP:0008872HP:0008872Feeding difficulties in infancy0MT-CO3 CL E G H4514550ORPHA07422516050
HP:0008872HP:0008872Feeding difficulties in infancy0MT-ND1 CL E G H4535550ORPHA07455516000
HP:0008872HP:0008872Feeding difficulties in infancy0MT-ND4 CL E G H4538550ORPHA07459516003
HP:0008872HP:0008872Feeding difficulties in infancy0MT-ND5 CL E G H4540550ORPHA07461516005
HP:0008872HP:0008872Feeding difficulties in infancy0MT-ND6 CL E G H4541550ORPHA07462516006
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TF CL E G H4558550ORPHA07481590070
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TH CL E G H4564550ORPHA07487590040
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TL1 CL E G H4567550ORPHA07490590050
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TQ CL E G H4572550ORPHA07495590030
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TS1 CL E G H4574550ORPHA07497590080
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TS2 CL E G H4575550ORPHA07498590085
HP:0008872HP:0008872Feeding difficulties in infancy0MT-TW CL E G H4578550ORPHA07501590095
HP:0008872HP:0008872Feeding difficulties in infancy0PIEZO2 CL E G H63895617146Arthrogryposis, distal, with impaired proprioception and touch617146C4310692OMIM03232926270613629
HP:0008872HP:0008872Feeding difficulties in infancy0PRKCSH CL E G H55892924Hypoplastic thumbs hydranencephalyORPHA0281199411177060
HP:0008872HP:0008872Feeding difficulties in infancy0PSAP CL E G H5660309256ORPHA0272209498176801
HP:0008872HP:0008872Feeding difficulties in infancy0RAC1 CL E G H5879617751MENTAL RETARDATION, AUTOSOMAL DOMINANT 48617751C4540321OMIM017699801602048
HP:0008872HP:0008872Feeding difficulties in infancy0RREB1 CL E G H6239567ORPHA01217110449602209
HP:0008872HP:0008872Feeding difficulties in infancy0SCN4A CL E G H6329682ORPHA012984810591603967
HP:0008872HP:0008872Feeding difficulties in infancy0SDHA CL E G H63893208ORPHA091127910680600857
HP:0008872HP:0008872Feeding difficulties in infancy0SDHAF1 CL E G H6440963208ORPHA064033867612848
HP:0008872HP:0008872Feeding difficulties in infancy0SDHB CL E G H63903208ORPHA027966710681185470
HP:0008872HP:0008872Feeding difficulties in infancy0SDHD CL E G H63923208ORPHA017436110683602690
HP:0008872HP:0008872Feeding difficulties in infancy0SEC24C CL E G H9632567ORPHA02410705607185
HP:0008872HP:0008872Feeding difficulties in infancy0SEC63 CL E G H112312924Hypoplastic thumbs hydranencephalyORPHA02322721082608648
HP:0008872HP:0008872Feeding difficulties in infancy0SH3BP2 CL E G H6452184ORPHA01641110825602104
HP:0008872HP:0008872Feeding difficulties in infancy0SKI CL E G H6497182212Shprintzen-Goldberg syndrome182212C1321551OMIM02450210896164780
HP:0008872HP:0008872Feeding difficulties in infancy0TBX1 CL E G H6899567ORPHA08255311592602054
HP:0008872HP:0008872Feeding difficulties in infancy0TGFB1 CL E G H70401328Chromosome 15 ringCN035931ORPHA0354711766190180
HP:0008872HP:0008872Feeding difficulties in infancy0TRAF3IP2 CL E G H107581334ORPHA05911343607043
HP:0008872HP:0008872Feeding difficulties in infancy0TTC21B CL E G H79809474ORPHA06333425660612014
HP:0008872HP:0008872Feeding difficulties in infancy0UBE3B CL E G H89910244450Kaufman oculocerebrofacial syndrome244450C1855663OMIM0255413478608047
HP:0008872HP:0008872Feeding difficulties in infancy0UFD1 CL E G H7353567ORPHA0436812520601754
HP:0008872HP:0008872Feeding difficulties in infancy0WASHC5 CL E G H98977Typical Joubert syndrome MRI findingsCN228298ORPHA02026828984610657
HP:0008872HP:0008872Feeding difficulties in infancy0WDR19 CL E G H57728474ORPHA04529418340608151
HP:0008872HP:0008872Feeding difficulties in infancy0WDR34 CL E G H89891474ORPHA02128296613363
HP:0008872HP:0008872Feeding difficulties in infancy0WDR60 CL E G H55112474ORPHA01321862615462
HP:0008872HP:0008872Feeding difficulties in infancy1AIFM1 CL E G H9131238329ORPHA0333438768300169
HP:0008872HP:0008872Feeding difficulties in infancy1ARSA CL E G H410309256ORPHA0254567713607574
HP:0008872HP:0008872Feeding difficulties in infancy1ARVCF CL E G H421567ORPHA02477728602269
HP:0008872HP:0008872Feeding difficulties in infancy1ATRX CL E G H546847ORPHA0170663886300032
HP:0008872HP:0008872Feeding difficulties in infancy1BCOR CL E G H548802712HMG CoA synthetase deficiencyCN072869ORPHA05541520893300485
HP:0008872HP:0008872Feeding difficulties in infancy1CASK CL E G H8573300422FG syndrome 4300422CN033933OMIM01194461497300172
HP:0008872HP:0008872Feeding difficulties in infancy1CCDC22 CL E G H289527Typical Joubert syndrome MRI findingsCN228298ORPHA0722128909300859
HP:0008872HP:0008872Feeding difficulties in infancy1CEP120 CL E G H153241474ORPHA098726690613446
HP:0008872HP:0008872Feeding difficulties in infancy1CLEC7A CL E G H645811334ORPHA014514558606264
HP:0008872HP:0008872Feeding difficulties in infancy1COL1A1 CL E G H12771310ORPHA096711052197120150
HP:0008872HP:0008872Feeding difficulties in infancy1COMT CL E G H1312567ORPHA0155552228116790
HP:0008872HP:0008872Feeding difficulties in infancy1DYNC2H1 CL E G H79659474ORPHA02078892962603297
HP:0008872HP:0008872Feeding difficulties in infancy1DYNC2LI1 CL E G H51626474ORPHA01417324595617083
HP:0008872HP:0008872Feeding difficulties in infancy1DYRK1A CL E G H1859614104Mental retardation, autosomal dominant 7614104C3279839OMIM0774373091600855
HP:0008872HP:0008872Feeding difficulties in infancy1EPG5 CL E G H577241493Congenital mesoblastic nephromaORPHA06849529331615068
HP:0008872HP:0008872Feeding difficulties in infancy1GP1BB CL E G H2812567ORPHA0534044440138720
HP:0008872HP:0008872Feeding difficulties in infancy1HADH CL E G H303371212ORPHA026944799601609
HP:0008872HP:0008872Feeding difficulties in infancy1HDAC8 CL E G H55869300882Cornelia de Lange syndrome 5300882C3550903OMIM05622713315300269
HP:0008872HP:0008872Feeding difficulties in infancy1HIRA CL E G H7290567ORPHA053994916600237
HP:0008872HP:0008872Feeding difficulties in infancy1HSPG2 CL E G H3339800ORPHA0678625273142461
HP:0008872HP:0008872Feeding difficulties in infancy1IFT140 CL E G H9742474ORPHA07253029077614620
HP:0008872HP:0008872Feeding difficulties in infancy1IFT172 CL E G H26160474ORPHA02726930391607386
HP:0008872HP:0008872Feeding difficulties in infancy1IFT80 CL E G H57560474ORPHA01321129262611177
HP:0008872HP:0008872Feeding difficulties in infancy1IL17F CL E G H1127441334ORPHA056016404606496
HP:0008872HP:0008872Feeding difficulties in infancy1IL17RA CL E G H237651334ORPHA0195005985605461
HP:0008872HP:0008872Feeding difficulties in infancy1IL17RC CL E G H848181334ORPHA0421718358610925
HP:0008872HP:0008872Feeding difficulties in infancy1JMJD1C CL E G H221037567ORPHA02950912313604503
HP:0008872HP:0008872Feeding difficulties in infancy1LRP5 CL E G H40412924Hypoplastic thumbs hydranencephalyORPHA02214116697603506
HP:0008872HP:0008872Feeding difficulties in infancy1MAP3K7 CL E G H6885617137Frontometaphyseal dysplasia 2617137C4310697OMIM013646859602614
HP:0008872HP:0008872Feeding difficulties in infancy1MT-CO1 CL E G H4512550ORPHA07419516030
HP:0008872HP:0008872Feeding difficulties in infancy1MT-CO2 CL E G H4513550ORPHA07421516040
HP:0008872HP:0008872Feeding difficulties in infancy1MT-CO3 CL E G H4514550ORPHA07422516050
HP:0008872HP:0008872Feeding difficulties in infancy1MT-ND1 CL E G H4535550ORPHA07455516000
HP:0008872HP:0008872Feeding difficulties in infancy1MT-ND4 CL E G H4538550ORPHA07459516003
HP:0008872HP:0008872Feeding difficulties in infancy1MT-ND5 CL E G H4540550ORPHA07461516005
HP:0008872HP:0008872Feeding difficulties in infancy1MT-ND6 CL E G H4541550ORPHA07462516006
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TF CL E G H4558550ORPHA07481590070
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TH CL E G H4564550ORPHA07487590040
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TL1 CL E G H4567550ORPHA07490590050
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TQ CL E G H4572550ORPHA07495590030
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TS1 CL E G H4574550ORPHA07497590080
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TS2 CL E G H4575550ORPHA07498590085
HP:0008872HP:0008872Feeding difficulties in infancy1MT-TW CL E G H4578550ORPHA07501590095
HP:0008872HP:0008872Feeding difficulties in infancy1PIEZO2 CL E G H63895617146Arthrogryposis, distal, with impaired proprioception and touch617146C4310692OMIM03232926270613629
HP:0008872HP:0008872Feeding difficulties in infancy1PRKCSH CL E G H55892924Hypoplastic thumbs hydranencephalyORPHA0281199411177060
HP:0008872HP:0008872Feeding difficulties in infancy1PSAP CL E G H5660309256ORPHA0272209498176801
HP:0008872HP:0008872Feeding difficulties in infancy1RAC1 CL E G H5879617751MENTAL RETARDATION, AUTOSOMAL DOMINANT 48617751C4540321OMIM017699801602048
HP:0008872HP:0008872Feeding difficulties in infancy1RREB1 CL E G H6239567ORPHA01217110449602209
HP:0008872HP:0008872Feeding difficulties in infancy1SCN4A CL E G H6329682ORPHA012984810591603967
HP:0008872HP:0008872Feeding difficulties in infancy1SDHA CL E G H63893208ORPHA091127910680600857
HP:0008872HP:0008872Feeding difficulties in infancy1SDHAF1 CL E G H6440963208ORPHA064033867612848
HP:0008872HP:0008872Feeding difficulties in infancy1SDHB CL E G H63903208ORPHA027966710681185470
HP:0008872HP:0008872Feeding difficulties in infancy1SDHD CL E G H63923208ORPHA017436110683602690
HP:0008872HP:0008872Feeding difficulties in infancy1SEC24C CL E G H9632567ORPHA02410705607185
HP:0008872HP:0008872Feeding difficulties in infancy1SEC63 CL E G H112312924Hypoplastic thumbs hydranencephalyORPHA02322721082608648
HP:0008872HP:0008872Feeding difficulties in infancy1SH3BP2 CL E G H6452184ORPHA01641110825602104
HP:0008872HP:0008872Feeding difficulties in infancy1SKI CL E G H6497182212Shprintzen-Goldberg syndrome182212C1321551OMIM02450210896164780
HP:0008872HP:0008872Feeding difficulties in infancy1TBX1 CL E G H6899567ORPHA08255311592602054
HP:0008872HP:0008872Feeding difficulties in infancy1TGFB1 CL E G H70401328Chromosome 15 ringCN035931ORPHA0354711766190180
HP:0008872HP:0008872Feeding difficulties in infancy1TRAF3IP2 CL E G H107581334ORPHA05911343607043
HP:0008872HP:0008872Feeding difficulties in infancy1TTC21B CL E G H79809474ORPHA06333425660612014
HP:0008872HP:0008872Feeding difficulties in infancy1UBE3B CL E G H89910244450Kaufman oculocerebrofacial syndrome244450C1855663OMIM0255413478608047
HP:0008872HP:0008872Feeding difficulties in infancy1UFD1 CL E G H7353567ORPHA0436812520601754
HP:0008872HP:0008872Feeding difficulties in infancy1WASHC5 CL E G H98977Typical Joubert syndrome MRI findingsCN228298ORPHA02026828984610657
HP:0008872HP:0008872Feeding difficulties in infancy1WDR19 CL E G H57728474ORPHA04529418340608151
HP:0008872HP:0008872Feeding difficulties in infancy1WDR34 CL E G H89891474ORPHA02128296613363
HP:0008872HP:0008872Feeding difficulties in infancy1WDR60 CL E G H55112474ORPHA01321862615462


Genes (340) :A2ML1 ACADS ACTA1 AGRN AHI1 AIFM1 APC2 AQP2 ARID1A ARID1B ARID2 ARL13B ARL3 ARMC9 ARSA ARVCF ARX ASL ASXL2 ATP6V0A2 ATP7A ATRX AVPR2 B3GLCT B9D1 BCKDHA BCKDHB BCOR BCS1L BIN1 BRAF BTD BUB1B CASK CASR CC2D2A CCDC22 CEP104 CEP120 CEP41 CHAT CHD7 CHRNA1 CHRNE CISD2 CLCF1 CLDN16 CLEC7A CNTN1 COL11A2 COL13A1 COL1A1 COL6A1 COL6A2 COL6A3 COLQ COMT COX1 COX2 COX3 CPLANE1 CPT1A CPT2 CREBBP CRLF1 CSPP1 CYP11B2 DBT DDC DEAF1 DGUOK DHCR7 DLEC1 DMPK DPF2 DPYS DYNC2H1 DYNC2LI1 DYRK1A EED EFTUD2 ELN ELP1 EMG1 EP300 EPG5 ERCC1 ERCC2 ERCC5 ERCC6 EZH2 FGFR2 FKRP FLCN FLI1 FLII FLNA GABRD GCDH GP1BB GPT2 HACD1 HADH HADHA HADHB HDAC8 HERC2 HIRA HLCS HRAS HSD17B4 HSPD1 HSPG2 HTRA2 HYLS1 IFT140 IFT172 IFT80 IGF2 IL17F IL17RA IL17RC INPP5E INSR IPW IQSEC2 ITGA7 JMJD1C KANSL1 KAT6B KCNAB2 KCNK9 KDM6A KIAA0556 KIAA0586 KIAA0753 KIF1A KIF7 KMT2A KMT2D KRAS LAMA2 LAMB2 LIFR LMBRD1 LRP5 LZTR1 MAGEL2 MAP2K1 MAP2K2 MAP3K20 MAP3K7 MBD5 MCCC1 MECP2 MKRN3 MKRN3-AS1 MKS1 MLXIPL MMAA MMAB MMACHC MOCS1 MOGS MRPS16 MTR MYH3 MYL2 MYO9A NALCN ND1 ND4 ND5 ND6 NDN NDUFS4 NIPBL NPAP1 NRAS NSD1 OCRL OFD1 OPA1 ORC1 PANK2 PAX8 PCCA PCCB PDE10A PDE6D PEX1 PEX10 PEX11B PEX12 PEX13 PEX14 PEX16 PEX19 PEX2 PEX26 PEX3 PEX5 PEX6 PHF6 PIBF1 PIEZO2 PIGN PLAA PLXND1 PMM2 PNPO PQBP1 PRDM16 PRDX1 PRKCSH PSAP PSAT1 PTPN11 PTS PUF60 PWAR1 PWRN1 RAB3GAP1 RAB3GAP2 RAC1 RAD21 RAF1 RAI1 RARS2 RASA2 RERE RETREG1 REV3L RHBDF2 RIT1 RNF6 RPGRIP1L RPS6KA3 RRAS RREB1 RYR1 SAMHD1 SCN4A SCN9A SCNN1A SCNN1B SCNN1G SCO2 SDHA SDHAF1 SDHB SDHD SEC24C SEC63 SELENON SEMA3E SETBP1 SETD2 SETD5 SH3BP2 SIK1 SIN3A SKI SLC16A2 SLC18A3 SLC25A1 SLC25A22 SLC46A1 SLC52A1 SLC5A7 SLC6A8 SLC9A6 SMARCA4 SMARCB1 SMARCE1 SMC1A SMC3 SMPD1 SNAP25 SNORD115-1 SNORD116-1 SNRPN SON SOS1 SOS2 SOX11 SRCAP ST3GAL5 SUCLA2 SUZ12 SYT2 TALDO1 TBC1D24 TBCK TBX1 TCTN1 TCTN2 TCTN3 TGFB1 TGFBR2 TK2 TMEM216 TMEM237 TMEM67 TPM2 TPM3 TRAF3IP2 TREX1 TRIP4 TRMU TRNE TRNF TRNH TRNL1 TRNQ TRNS1 TRNS2 TRNW TSEN54 TSFM TSPYL1 TTC21B TUBB3 TUBB6 TXN2 TXNL4A UBE3A UBE3B UFD1 VAMP1 VPS13B VRK1 WASHC5 WDR19 WDR34 WDR60 WFS1 WNK1 WWOX ZNHIT3

Diseases (200) :648 201470 161800 475 238329 821 125800 1465 135900 309256 567 300215 207900 617190 219200 565 847 304800 709 261540 248600 2712 124000 255200 115150 1340 253260 257300 300422 239200 1454 7 474 138 605809 3463 610313 248250 1334 1427 1310 254090 603034 550 2754 255120 608836 180849 272430 203400 608643 819 251880 818 99977 160900 222748 614104 3447 610536 194050 1764 223900 1270 1493 1466 87 606612 610883 2308 300048 1606 25 71212 231530 199 300882 253270 261515 612233 800 616489 508 610443 612292 147920 300867 201300 607855 3206 79284 277380 2924 617137 156200 210200 300673 251100 251110 277400 252150 606056 610498 250940 2053 193700 252010 534 300804 616896 224690 234200 218700 606054 912 614870 614859 614876 614862 127 617146 280633 570 212065 610090 610992 1387 212720 617751 192 255320 612952 682 264350 604377 3208 184 613406 182212 300523 229050 300352 85278 610759 257200 2044 609056 612073 1328 254875 609285 225750 613070 277470 610505 608800 300570 608572 105830 244450 193 216550 607596 260565 2020 98914 198 613706 254210 608930 612540 98915 270400 477673 746 176270 3071 218040 617248 494526 614866 214110 617527 309500 261640 508488 611523 2198 798 1935 615026 617143 500150 606003 79500 616900 486815 254864 617732 478029
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.