Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of digestive system physiology (HP:0025032)help
Parent Node:
expand
Abdominal symptom (HP:0011458)help
..Starting node
..expand
Nausea and vomiting (HP:0002017)help
Term ID: 2017
Name: Nausea and vomiting
Synonym: Nausea and vomiting
Definition: Nausea is a commonly encountered symptom that has been defined as an unpleasant painless subjective feeling that one will imminently vomit. Vomiting has been defined as the forceful expulsion of the contents of the stomach, duodenum, or jejunum through the oral cavity. While nausea and vomiting are often thought to exist on a temporal continuum, this is not always the case. There are situations when severe nausea may be present without emesis and less frequently, when emesis may be present without preceding nausea.
Comments:
Reference: HP:0002017
Genes and Diseases:
 
       Child Nodes:
........expandVomiting (HP:0002013) help
................... HP:0002572 Episodic vomiting
................... HP:0002587 Projectile vomiting
................... HP:0025089 Feculent vomiting
........expandNausea (HP:0002018) help

 Sister Nodes: 
..expandAbdominal distention (HP:0003270) help
..expandAbdominal pain (HP:0002027) help
..expandAbnormal bowel sounds (HP:0030142) help
..expandAnorexia (HP:0002039) help
..expandConstipation (HP:0002019) help
..expandDiarrhea (HP:0002014) help
..expandFeeding difficulties (HP:0011968) help
..expandMalnutrition (HP:0004395) help
..expandPoor appetite (HP:0004396) help
..expandProtein avoidance (HP:0002038) help
..expandScaphoid abdomen (HP:0025063) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0002017HP:0002017Nausea and vomiting0AASS CL E G H1015717366ORPHA:2203Hyperlysinemia15
HP:0002017HP:0002017Nausea and vomiting0ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancy415
HP:0002017HP:0002017Nausea and vomiting0ABCC8 CL E G H683359ORPHA:79134DEND syndrome245
HP:0002017HP:0002017Nausea and vomiting0ABCD1 CL E G H21561ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent135
HP:0002017HP:0002017Nausea and vomiting0ACAD8 CL E G H2703487ORPHA:79159Isobutyryl-CoA dehydrogenase deficiency58
HP:0002017HP:0002017Nausea and vomiting0ACADM CL E G H3489OMIM:201450Acyl-Coa dehydrogenase, medium-chain, deficiency of197
HP:0002017HP:0002017Nausea and vomiting0ACADM CL E G H3489ORPHA:42Medium chain acyl-CoA dehydrogenase deficiency197
HP:0002017HP:0002017Nausea and vomiting0ACADVL CL E G H3792ORPHA:26793Very long chain acyl-CoA dehydrogenase deficiency200
HP:0002017HP:0002017Nausea and vomiting0ACADVL CL E G H3792OMIM:201475Very long-chain acyl-CoA dehydrogenase deficiency200
HP:0002017HP:0002017Nausea and vomiting0ACAT1 CL E G H3893OMIM:203750Alpha-Methylacetoacetic aciduria91
HP:0002017HP:0002017Nausea and vomiting0ACAT1 CL E G H3893ORPHA:134Beta-ketothiolase deficiency91
HP:0002017HP:0002017Nausea and vomiting0ACSF3 CL E G H19732227288ORPHA:289504Combined malonic and methylmalonic acidemia68
HP:0002017HP:0002017Nausea and vomiting0ACSF3 CL E G H19732227288OMIM:614265Combined malonic and methylmalonic aciduria68
HP:0002017HP:0002017Nausea and vomiting0ACTG2 CL E G H72145ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent23
HP:0002017HP:0002017Nausea and vomiting0ACTG2 CL E G H72145OMIM:155310Visceral myopathy 123
HP:0002017HP:0002017Nausea and vomiting0ACY1 CL E G H95177ORPHA:137754Neurological conditions associated with aminoacylase 1 deficiency13
HP:0002017HP:0002017Nausea and vomiting0ADNP CL E G H2339415766ORPHA:404448ADNP syndrome47
HP:0002017HP:0002017Nausea and vomiting0AIMP1 CL E G H925510648OMIM:260600Leukodystrophy, hypomyelinating, 34
HP:0002017HP:0002017Nausea and vomiting0AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040282 - Frequent95
HP:0002017HP:0002017Nausea and vomiting0AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040282 - Frequent54
HP:0002017HP:0002017Nausea and vomiting0ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiency62
HP:0002017HP:0002017Nausea and vomiting0ALAD CL E G H210395OMIM:612740Porphyria, acute hepatic62
HP:0002017HP:0002017Nausea and vomiting0ALDH18A1 CL E G H58329722ORPHA:90348Autosomal dominant cutis laxa89
HP:0002017HP:0002017Nausea and vomiting0ALDH18A1 CL E G H58329722OMIM:601162Spastic paraplegia 9A, autosomal dominant89
HP:0002017HP:0002017Nausea and vomiting0ALDOB CL E G H229417OMIM:229600Fructose intolerance, hereditary73
HP:0002017HP:0002017Nausea and vomiting0ALDOB CL E G H229417ORPHA:469Hereditary fructose intolerance73
HP:0002017HP:0002017Nausea and vomiting0ALG11 CL E G H44013832456ORPHA:280071ALG11-CDG41
HP:0002017HP:0002017Nausea and vomiting0ALG11 CL E G H44013832456OMIM:613661Congenital disorder of glycosylation, type Ip41
HP:0002017HP:0002017Nausea and vomiting0ALG3 CL E G H1019523056OMIM:601110Congenital disorder of glycosylation, type Id37
HP:0002017HP:0002017Nausea and vomiting0ALG8 CL E G H7905323161ORPHA:79325ALG8-CDG46
HP:0002017HP:0002017Nausea and vomiting0ALG8 CL E G H7905323161OMIM:608104Congenital disorder of glycosylation, type Ih46
HP:0002017HP:0002017Nausea and vomiting0ALG9 CL E G H7979615672ORPHA:79328ALG9-CDG93
HP:0002017HP:0002017Nausea and vomiting0ALPL CL E G H249438OMIM:241500Hypophosphatasia, infantile126
HP:0002017HP:0002017Nausea and vomiting0ALX4 CL E G H60529450ORPHA:60015Enlarged parietal foramina132
HP:0002017HP:0002017Nausea and vomiting0AMN CL E G H8169314604ORPHA:35858Imerslund-Gräsbeck syndrome25
HP:0002017HP:0002017Nausea and vomiting0ANAPC1 CL E G H6468219988ORPHA:221008Rothmund-Thomson syndrome type 12
HP:0002017HP:0002017Nausea and vomiting0ANG CL E G H283483ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional32
HP:0002017HP:0002017Nausea and vomiting0ANO1 CL E G H5510721625OMIM:620045
HP:0002017HP:0002017Nausea and vomiting0ANXA11 CL E G H311535ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0APC CL E G H324583ORPHA:99818Turcot syndrome with polyposis3179
HP:0002017HP:0002017Nausea and vomiting0AQP2 CL E G H359634OMIM:125800Diabetes insipidus, nephrogenic, 275
HP:0002017HP:0002017Nausea and vomiting0AQP2 CL E G H359634ORPHA:223Nephrogenic diabetes insipidusHP:0040282 - Frequent75
HP:0002017HP:0002017Nausea and vomiting0ARG1 CL E G H383663OMIM:207800Argininemia31
HP:0002017HP:0002017Nausea and vomiting0ASL CL E G H435746OMIM:207900Argininosuccinic aciduria81
HP:0002017HP:0002017Nausea and vomiting0ASPA CL E G H443756ORPHA:314911Severe Canavan disease48
HP:0002017HP:0002017Nausea and vomiting0ASS1 CL E G H445758OMIM:215700Citrullinemia, classic119
HP:0002017HP:0002017Nausea and vomiting0ASXL1 CL E G H17102318318ORPHA:97297Bohring-Opitz syndrome145
HP:0002017HP:0002017Nausea and vomiting0ASXL1 CL E G H17102318318ORPHA:98849Systemic mastocytosis with associated hematologic neoplasm145
HP:0002017HP:0002017Nausea and vomiting0ASXL3 CL E G H8081629357OMIM:615485BAINBRIDGE-ROPERS SYNDROME; BRPS49
HP:0002017HP:0002017Nausea and vomiting0ATP1A2 CL E G H477800ORPHA:2131Alternating hemiplegia of childhood239
HP:0002017HP:0002017Nausea and vomiting0ATP1A2 CL E G H477800OMIM:602481Migraine, familial hemiplegic, 2239
HP:0002017HP:0002017Nausea and vomiting0ATP1A3 CL E G H478801ORPHA:2131Alternating hemiplegia of childhood150
HP:0002017HP:0002017Nausea and vomiting0ATP6 CL E G H45087414ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ATP6V0A4 CL E G H50617866OMIM:602722RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR64
HP:0002017HP:0002017Nausea and vomiting0ATP7A CL E G H538869ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent192
HP:0002017HP:0002017Nausea and vomiting0ATP7A CL E G H538869ORPHA:565Menkes diseaseHP:0040282 - Frequent192
HP:0002017HP:0002017Nausea and vomiting0ATP7B CL E G H540870OMIM:277900Wilson disease315
HP:0002017HP:0002017Nausea and vomiting0ATRX CL E G H546886ORPHA:847Alpha-thalassemia-X-linked intellectual disability syndromeHP:0040283 - Occasional169
HP:0002017HP:0002017Nausea and vomiting0ATRX CL E G H546886OMIM:309580Mental retardation-hypotonic facies syndrome, X-linked, 1169
HP:0002017HP:0002017Nausea and vomiting0ATRX CL E G H546886ORPHA:100075Neuroendocrine tumor of stomachHP:0040282 - Frequent169
HP:0002017HP:0002017Nausea and vomiting0ATXN2 CL E G H631110555ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional11
HP:0002017HP:0002017Nausea and vomiting0AVP CL E G H551894ORPHA:30925Hereditary central diabetes insipidus22
HP:0002017HP:0002017Nausea and vomiting0AVPR2 CL E G H554897OMIM:304800Diabetes insipidus, nephrogenic, X-linked67
HP:0002017HP:0002017Nausea and vomiting0AVPR2 CL E G H554897ORPHA:223Nephrogenic diabetes insipidusHP:0040282 - Frequent67
HP:0002017HP:0002017Nausea and vomiting0BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040282 - Frequent184
HP:0002017HP:0002017Nausea and vomiting0BAZ1B CL E G H9031961ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0BCKDHA CL E G H593986OMIM:248600Maple syrup urine disease120
HP:0002017HP:0002017Nausea and vomiting0BCKDHB CL E G H594987OMIM:248600Maple syrup urine disease162
HP:0002017HP:0002017Nausea and vomiting0BCL10 CL E G H8915989ORPHA:52417MALT lymphomaHP:0040281 - Very frequent18
HP:0002017HP:0002017Nausea and vomiting0BCL7B CL E G H92751005ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0BIRC3 CL E G H330591ORPHA:52417MALT lymphomaHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0BMPR1A CL E G H6571076ORPHA:440437Familial colorectal cancer Type XHP:0040282 - Frequent385
HP:0002017HP:0002017Nausea and vomiting0BOLA3 CL E G H38896224415OMIM:614299Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia14
HP:0002017HP:0002017Nausea and vomiting0BRAF CL E G H6731097OMIM:115150Cardiofaciocutaneous syndrome 1276
HP:0002017HP:0002017Nausea and vomiting0BRAF CL E G H6731097ORPHA:54595CraniopharyngiomaHP:0040282 - Frequent276
HP:0002017HP:0002017Nausea and vomiting0BRCA1 CL E G H6721100ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional5769
HP:0002017HP:0002017Nausea and vomiting0BRCA1 CL E G H6721100ORPHA:168829Primary peritoneal carcinomaHP:0040281 - Very frequent5769
HP:0002017HP:0002017Nausea and vomiting0BRCA2 CL E G H6751101ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional7642
HP:0002017HP:0002017Nausea and vomiting0BSND CL E G H780916512ORPHA:89938Infantile Bartter syndrome with sensorineural deafness53
HP:0002017HP:0002017Nausea and vomiting0BTD CL E G H6861122OMIM:253260Biotinidase deficiencymultiple carboxylase deficiency, late-onset223
HP:0002017HP:0002017Nausea and vomiting0BUD23 CL E G H11404916405ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0C4A CL E G H7201323ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0002017HP:0002017Nausea and vomiting0C9ORF72 CL E G H20322828337ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional56
HP:0002017HP:0002017Nausea and vomiting0CACNA1A CL E G H7731388ORPHA:2131Alternating hemiplegia of childhood449
HP:0002017HP:0002017Nausea and vomiting0CACNA1A CL E G H7731388ORPHA:71518Benign paroxysmal torticollis of infancy449
HP:0002017HP:0002017Nausea and vomiting0CACNA1A CL E G H7731388ORPHA:97Familial paroxysmal ataxiaHP:0040282 - Frequent449
HP:0002017HP:0002017Nausea and vomiting0CACNA1D CL E G H7761391ORPHA:369929Primary hyperaldosteronism-seizures-neurological abnormalities syndrome51
HP:0002017HP:0002017Nausea and vomiting0CARD8 CL E G H2290017057OMIM:619079INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 30; IBD301
HP:0002017HP:0002017Nausea and vomiting0CAV1 CL E G H8571527ORPHA:220393Diffuse cutaneous systemic sclerosisHP:0040283 - Occasional11
HP:0002017HP:0002017Nausea and vomiting0CAV1 CL E G H8571527ORPHA:220402Limited cutaneous systemic sclerosisHP:0040282 - Frequent11
HP:0002017HP:0002017Nausea and vomiting0CAV1 CL E G H8571527OMIM:606721Lipodystrophy, familial partial, type 711
HP:0002017HP:0002017Nausea and vomiting0CCM2 CL E G H8360521708ORPHA:221061Familial cerebral cavernous malformation37
HP:0002017HP:0002017Nausea and vomiting0CCN2 CL E G H14902500ORPHA:220393Diffuse cutaneous systemic sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0CCN2 CL E G H14902500ORPHA:220402Limited cutaneous systemic sclerosisHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0CCNF CL E G H8991591ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0CCR1 CL E G H12301602ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0CCR6 CL E G H12351607ORPHA:220393Diffuse cutaneous systemic sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0CCR6 CL E G H12351607ORPHA:220402Limited cutaneous systemic sclerosisHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0CD46 CL E G H41796953ORPHA:244242HELLP syndrome39
HP:0002017HP:0002017Nausea and vomiting0CD55 CL E G H16042665OMIM:226300Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy9
HP:0002017HP:0002017Nausea and vomiting0CDC42BPB CL E G H95781738OMIM:619841
HP:0002017HP:0002017Nausea and vomiting0CDC73 CL E G H7957716783ORPHA:99880Hyperparathyroidism-jaw tumor syndromeHP:0040283 - Occasional169
HP:0002017HP:0002017Nausea and vomiting0CDC73 CL E G H7957716783ORPHA:143Parathyroid carcinomaHP:0040283 - Occasional169
HP:0002017HP:0002017Nausea and vomiting0CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040282 - Frequent636
HP:0002017HP:0002017Nausea and vomiting0CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040282 - Frequent636
HP:0002017HP:0002017Nausea and vomiting0CDK13 CL E G H86211733OMIM:617360Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder8
HP:0002017HP:0002017Nausea and vomiting0CDK8 CL E G H10241779OMIM:618748INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA
HP:0002017HP:0002017Nausea and vomiting0CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 12
HP:0002017HP:0002017Nausea and vomiting0CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1102
HP:0002017HP:0002017Nausea and vomiting0CDKN2A CL E G H10291787ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional289
HP:0002017HP:0002017Nausea and vomiting0CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 11
HP:0002017HP:0002017Nausea and vomiting0CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1
HP:0002017HP:0002017Nausea and vomiting0CDON CL E G H5093717104ORPHA:93925Alobar holoprosencephaly200
HP:0002017HP:0002017Nausea and vomiting0CDON CL E G H5093717104ORPHA:93924Lobar holoprosencephaly200
HP:0002017HP:0002017Nausea and vomiting0CDON CL E G H5093717104ORPHA:93926Midline interhemispheric variant of holoprosencephaly200
HP:0002017HP:0002017Nausea and vomiting0CDON CL E G H5093717104ORPHA:220386Semilobar holoprosencephaly200
HP:0002017HP:0002017Nausea and vomiting0CFAP410 CL E G H7551260ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0CFH CL E G H30754883ORPHA:244242HELLP syndrome86
HP:0002017HP:0002017Nausea and vomiting0CFI CL E G H34265394ORPHA:244242HELLP syndrome57
HP:0002017HP:0002017Nausea and vomiting0CHCHD10 CL E G H40091615559ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional11
HP:0002017HP:0002017Nausea and vomiting0CHMP2B CL E G H2597824537ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional42
HP:0002017HP:0002017Nausea and vomiting0CLCN2 CL E G H11812020ORPHA:404Familial hyperaldosteronism type II44
HP:0002017HP:0002017Nausea and vomiting0CLCNKA CL E G H11872026ORPHA:89938Infantile Bartter syndrome with sensorineural deafness9
HP:0002017HP:0002017Nausea and vomiting0CLCNKB CL E G H11882027ORPHA:358Gitelman syndromeHP:0040283 - Occasional27
HP:0002017HP:0002017Nausea and vomiting0CLCNKB CL E G H11882027ORPHA:89938Infantile Bartter syndrome with sensorineural deafness27
HP:0002017HP:0002017Nausea and vomiting0CLIP2 CL E G H74612586ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0CLMP CL E G H7982724039OMIM:615237Congenital short bowel syndrome7
HP:0002017HP:0002017Nausea and vomiting0COA8 CL E G H8433420492ORPHA:436271Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy
HP:0002017HP:0002017Nausea and vomiting0COL1A1 CL E G H12772197ORPHA:287Classical Ehlers-Danlos syndrome373
HP:0002017HP:0002017Nausea and vomiting0COL4A5 CL E G H12872207ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosis678
HP:0002017HP:0002017Nausea and vomiting0COL4A6 CL E G H12882208ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosis18
HP:0002017HP:0002017Nausea and vomiting0COL5A1 CL E G H12892209ORPHA:287Classical Ehlers-Danlos syndrome660
HP:0002017HP:0002017Nausea and vomiting0COL5A2 CL E G H12902210ORPHA:287Classical Ehlers-Danlos syndrome325
HP:0002017HP:0002017Nausea and vomiting0COQ2 CL E G H2723525223OMIM:607426Coenzyme Q10 deficiency, primary, 154
HP:0002017HP:0002017Nausea and vomiting0COQ2 CL E G H2723525223ORPHA:255249Leigh syndrome with nephrotic syndrome54
HP:0002017HP:0002017Nausea and vomiting0COX1 CL E G H45127419ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0COX2 CL E G H45137421ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0COX3 CL E G H45147422ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0CPOX CL E G H13712321OMIM:121300Coproporphyria72
HP:0002017HP:0002017Nausea and vomiting0CPOX CL E G H13712321OMIM:618892Harderoporphyria72
HP:0002017HP:0002017Nausea and vomiting0CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyria72
HP:0002017HP:0002017Nausea and vomiting0CPS1 CL E G H13732323OMIM:237300Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to124
HP:0002017HP:0002017Nausea and vomiting0CPT2 CL E G H13762330OMIM:600649Carnitine palmitoyltransferase II deficiency, infantile101
HP:0002017HP:0002017Nausea and vomiting0CPT2 CL E G H13762330OMIM:608836Carnitine palmitoyltransferase II deficiency, lethal neonatal101
HP:0002017HP:0002017Nausea and vomiting0CTLA4 CL E G H14932505ORPHA:900Granulomatosis with polyangiitisHP:0040282 - Frequent10
HP:0002017HP:0002017Nausea and vomiting0CTNNB1 CL E G H14992514ORPHA:54595CraniopharyngiomaHP:0040282 - Frequent88
HP:0002017HP:0002017Nausea and vomiting0CTNNB1 CL E G H14992514ORPHA:33402Pediatric hepatocellular carcinoma88
HP:0002017HP:0002017Nausea and vomiting0CTNS CL E G H14972518ORPHA:411629Infantile nephropathic cystinosis178
HP:0002017HP:0002017Nausea and vomiting0CTNS CL E G H14972518ORPHA:411634Juvenile nephropathic cystinosis178
HP:0002017HP:0002017Nausea and vomiting0CTRC CL E G H113302523ORPHA:103918Tropical pancreatitis39
HP:0002017HP:0002017Nausea and vomiting0CUBN CL E G H80292548ORPHA:35858Imerslund-Gräsbeck syndrome273
HP:0002017HP:0002017Nausea and vomiting0CYC1 CL E G H15372579OMIM:615453Mitochondrial complex III deficiency, nuclear type 612
HP:0002017HP:0002017Nausea and vomiting0CYP11A1 CL E G H15832590ORPHA:16855846,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency31
HP:0002017HP:0002017Nausea and vomiting0CYP11A1 CL E G H15832590ORPHA:289548Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency31
HP:0002017HP:0002017Nausea and vomiting0CYP11B1 CL E G H15842591ORPHA:403Familial hyperaldosteronism type I112
HP:0002017HP:0002017Nausea and vomiting0CYP11B2 CL E G H15852592OMIM:203400Corticosterone methyloxidase type I deficiency73
HP:0002017HP:0002017Nausea and vomiting0CYP11B2 CL E G H15852592ORPHA:556030Early-onset familial hypoaldosteronism73
HP:0002017HP:0002017Nausea and vomiting0CYP11B2 CL E G H15852592ORPHA:403Familial hyperaldosteronism type I73
HP:0002017HP:0002017Nausea and vomiting0CYP24A1 CL E G H15912602OMIM:143880Hypercalcemia, infantile, 173
HP:0002017HP:0002017Nausea and vomiting0CYTB CL E G H45197427ORPHA:137675Histiocytoid cardiomyopathy
HP:0002017HP:0002017Nausea and vomiting0CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0D2HGDH CL E G H72829428358OMIM:600721D-2-Hydroxyglutaric aciduria 1102
HP:0002017HP:0002017Nausea and vomiting0DAO CL E G H16102671ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0DAXX CL E G H16162681ORPHA:100075Neuroendocrine tumor of stomachHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0DBH CL E G H16212689ORPHA:230Dopamine beta-hydroxylase deficiency80
HP:0002017HP:0002017Nausea and vomiting0DBT CL E G H16292698OMIM:248600Maple syrup urine disease156
HP:0002017HP:0002017Nausea and vomiting0DCTN1 CL E G H16392711ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional86
HP:0002017HP:0002017Nausea and vomiting0DGAT1 CL E G H86942843OMIM:615863Diarrhea 7, protein-losing Enteropathy type9
HP:0002017HP:0002017Nausea and vomiting0DGUOK CL E G H17162858OMIM:251880Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)57
HP:0002017HP:0002017Nausea and vomiting0DHCR7 CL E G H17172860OMIM:270400Smith-Lemli-Opitz syndrome159
HP:0002017HP:0002017Nausea and vomiting0DISP1 CL E G H8497619711ORPHA:93925Alobar holoprosencephaly22
HP:0002017HP:0002017Nausea and vomiting0DISP1 CL E G H8497619711ORPHA:93924Lobar holoprosencephaly22
HP:0002017HP:0002017Nausea and vomiting0DISP1 CL E G H8497619711ORPHA:93926Midline interhemispheric variant of holoprosencephaly22
HP:0002017HP:0002017Nausea and vomiting0DISP1 CL E G H8497619711ORPHA:220386Semilobar holoprosencephaly22
HP:0002017HP:0002017Nausea and vomiting0DLD CL E G H17382898ORPHA:2394Pyruvate dehydrogenase E3 deficiency89
HP:0002017HP:0002017Nausea and vomiting0DLEC1 CL E G H99402899ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0DLL1 CL E G H285142908ORPHA:93925Alobar holoprosencephaly3
HP:0002017HP:0002017Nausea and vomiting0DLL1 CL E G H285142908ORPHA:93924Lobar holoprosencephaly3
HP:0002017HP:0002017Nausea and vomiting0DLL1 CL E G H285142908ORPHA:93926Midline interhemispheric variant of holoprosencephaly3
HP:0002017HP:0002017Nausea and vomiting0DLL1 CL E G H285142908ORPHA:220386Semilobar holoprosencephaly3
HP:0002017HP:0002017Nausea and vomiting0DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paraganglioma
HP:0002017HP:0002017Nausea and vomiting0DNAJC30 CL E G H8427716410ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0DNAJC6 CL E G H982915469ORPHA:2828Young-onset Parkinson disease6
HP:0002017HP:0002017Nausea and vomiting0DNASE1L3 CL E G H17762959ORPHA:36412Hypocomplementemic urticarial vasculitisHP:0040282 - Frequent3
HP:0002017HP:0002017Nausea and vomiting0DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma44
HP:0002017HP:0002017Nausea and vomiting0DOLK CL E G H2284523406OMIM:610768Congenital disorder of glycosylation, type Im55
HP:0002017HP:0002017Nausea and vomiting0DYRK1A CL E G H18593091ORPHA:464311Intellectual disability syndrome due to a DYRK1A point mutation134
HP:0002017HP:0002017Nausea and vomiting0ECE1 CL E G H18893146ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent13
HP:0002017HP:0002017Nausea and vomiting0EDN3 CL E G H19083178ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent67
HP:0002017HP:0002017Nausea and vomiting0EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 13
HP:0002017HP:0002017Nausea and vomiting0EDNRB CL E G H19103180ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent55
HP:0002017HP:0002017Nausea and vomiting0EGFR CL E G H19563236OMIM:616069Inflammatory skin and bowel disease, neonatal, 2257
HP:0002017HP:0002017Nausea and vomiting0EIF4H CL E G H745812741ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0ELN CL E G H20063327ORPHA:90348Autosomal dominant cutis laxa172
HP:0002017HP:0002017Nausea and vomiting0ELN CL E G H20063327ORPHA:904Williams syndromeHP:0040282 - Frequent172
HP:0002017HP:0002017Nausea and vomiting0ELP1 CL E G H85185959OMIM:223900Neuropathy, hereditary sensory and autonomic, type III133
HP:0002017HP:0002017Nausea and vomiting0ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancy151
HP:0002017HP:0002017Nausea and vomiting0EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma112
HP:0002017HP:0002017Nausea and vomiting0EPCAM CL E G H407211529ORPHA:92050Congenital tufting enteropathy170
HP:0002017HP:0002017Nausea and vomiting0EPCAM CL E G H407211529ORPHA:144Lynch syndromeHP:0040282 - Frequent170
HP:0002017HP:0002017Nausea and vomiting0EPHA4 CL E G H20433388ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional4
HP:0002017HP:0002017Nausea and vomiting0ERAP1 CL E G H5175218173ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0002017HP:0002017Nausea and vomiting0ERBB2 CL E G H20643430ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent77
HP:0002017HP:0002017Nausea and vomiting0ERBB3 CL E G H20653431ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent12
HP:0002017HP:0002017Nausea and vomiting0ERBB3 CL E G H20653431OMIM:243180Visceral neuropathy, familial, autosomal recessive12
HP:0002017HP:0002017Nausea and vomiting0ERBB4 CL E G H20663432ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional15
HP:0002017HP:0002017Nausea and vomiting0ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 113
HP:0002017HP:0002017Nausea and vomiting0ETFA CL E G H21083481OMIM:231680Multiple acyl-coa dehydrogenase deficiency37
HP:0002017HP:0002017Nausea and vomiting0ETFB CL E G H21093482OMIM:231680Multiple acyl-coa dehydrogenase deficiency27
HP:0002017HP:0002017Nausea and vomiting0ETFDH CL E G H21103483OMIM:231680Multiple acyl-coa dehydrogenase deficiency77
HP:0002017HP:0002017Nausea and vomiting0EWSR1 CL E G H21303508ORPHA:83469Desmoplastic small round cell tumorHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0EXT2 CL E G H21323513ORPHA:466926Seizures-scoliosis-macrocephaly syndrome102
HP:0002017HP:0002017Nausea and vomiting0F12 CL E G H21613530OMIM:610618ANGIOEDEMA, HEREDITARY, TYPE III; HAE328
HP:0002017HP:0002017Nausea and vomiting0FAH CL E G H21843579OMIM:276700Tyrosinemia, type I107
HP:0002017HP:0002017Nausea and vomiting0FAN1 CL E G H2290929170ORPHA:144Lynch syndromeHP:0040282 - Frequent15
HP:0002017HP:0002017Nausea and vomiting0FARSB CL E G H1005617800OMIM:613658Rajab interstitial lung disease with brain calcifications
HP:0002017HP:0002017Nausea and vomiting0FAS CL E G H35511920ORPHA:117Behçet diseaseHP:0040281 - Very frequent59
HP:0002017HP:0002017Nausea and vomiting0FBLN5 CL E G H105163602ORPHA:90348Autosomal dominant cutis laxa63
HP:0002017HP:0002017Nausea and vomiting0FBP1 CL E G H22033606ORPHA:348Fructose-1,6-bisphosphatase deficiency64
HP:0002017HP:0002017Nausea and vomiting0FGF8 CL E G H22533686ORPHA:93925Alobar holoprosencephaly17
HP:0002017HP:0002017Nausea and vomiting0FGF8 CL E G H22533686ORPHA:93924Lobar holoprosencephaly17
HP:0002017HP:0002017Nausea and vomiting0FGF8 CL E G H22533686ORPHA:93926Midline interhemispheric variant of holoprosencephaly17
HP:0002017HP:0002017Nausea and vomiting0FGF8 CL E G H22533686ORPHA:220386Semilobar holoprosencephaly17
HP:0002017HP:0002017Nausea and vomiting0FGFR1 CL E G H22603688ORPHA:93924Lobar holoprosencephaly172
HP:0002017HP:0002017Nausea and vomiting0FGFR1 CL E G H22603688ORPHA:220386Semilobar holoprosencephaly172
HP:0002017HP:0002017Nausea and vomiting0FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paraganglioma301
HP:0002017HP:0002017Nausea and vomiting0FIG4 CL E G H989616873ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional111
HP:0002017HP:0002017Nausea and vomiting0FKBP6 CL E G H84683722ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0FLI1 CL E G H23133749ORPHA:370348Peripheral primitive neuroectodermal tumorHP:0040283 - Occasional8
HP:0002017HP:0002017Nausea and vomiting0FLNA CL E G H23163754OMIM:300048Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked493
HP:0002017HP:0002017Nausea and vomiting0FOCAD CL E G H5491423377OMIM:6199913
HP:0002017HP:0002017Nausea and vomiting0FOXH1 CL E G H89283814ORPHA:93925Alobar holoprosencephaly48
HP:0002017HP:0002017Nausea and vomiting0FOXH1 CL E G H89283814ORPHA:93924Lobar holoprosencephaly48
HP:0002017HP:0002017Nausea and vomiting0FOXH1 CL E G H89283814ORPHA:93926Midline interhemispheric variant of holoprosencephaly48
HP:0002017HP:0002017Nausea and vomiting0FOXH1 CL E G H89283814ORPHA:220386Semilobar holoprosencephaly48
HP:0002017HP:0002017Nausea and vomiting0FOXP1 CL E G H270863823ORPHA:52417MALT lymphomaHP:0040281 - Very frequent184
HP:0002017HP:0002017Nausea and vomiting0FOXP3 CL E G H509436106ORPHA:37042Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome32
HP:0002017HP:0002017Nausea and vomiting0FOXRED1 CL E G H5557226927ORPHA:2609Isolated complex I deficiency61
HP:0002017HP:0002017Nausea and vomiting0FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndromeHP:0040281 - Very frequent50
HP:0002017HP:0002017Nausea and vomiting0FSHR CL E G H24923969OMIM:608115Ovarian hyperstimulation syndrome50
HP:0002017HP:0002017Nausea and vomiting0FUS CL E G H25214010ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional105
HP:0002017HP:0002017Nausea and vomiting0GALC CL E G H25814115ORPHA:206436Infantile Krabbe disease160
HP:0002017HP:0002017Nausea and vomiting0GALC CL E G H25814115OMIM:245200Krabbe disease160
HP:0002017HP:0002017Nausea and vomiting0GALE CL E G H25824116OMIM:230350Galactose epimerase deficiency52
HP:0002017HP:0002017Nausea and vomiting0GALT CL E G H25924135ORPHA:79239Classic galactosemia351
HP:0002017HP:0002017Nausea and vomiting0GALT CL E G H25924135OMIM:230400GALACTOSEMIA351
HP:0002017HP:0002017Nausea and vomiting0GAMT CL E G H25934136OMIM:612736Cerebral creatine deficiency syndrome 291
HP:0002017HP:0002017Nausea and vomiting0GAN CL E G H81394137OMIM:256850Giant axonal neuropathy 1, autosomal recessive121
HP:0002017HP:0002017Nausea and vomiting0GAS1 CL E G H26194165ORPHA:93925Alobar holoprosencephaly2
HP:0002017HP:0002017Nausea and vomiting0GAS1 CL E G H26194165ORPHA:93924Lobar holoprosencephaly2
HP:0002017HP:0002017Nausea and vomiting0GAS1 CL E G H26194165ORPHA:93926Midline interhemispheric variant of holoprosencephaly2
HP:0002017HP:0002017Nausea and vomiting0GAS1 CL E G H26194165ORPHA:220386Semilobar holoprosencephaly2
HP:0002017HP:0002017Nausea and vomiting0GATA2 CL E G H26244171ORPHA:3226Deafness-lymphedema-leukemia syndromeHP:0040282 - Frequent137
HP:0002017HP:0002017Nausea and vomiting0GDNF CL E G H26684232ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent59
HP:0002017HP:0002017Nausea and vomiting0GFAP CL E G H26704235ORPHA:363717Alexander disease type I188
HP:0002017HP:0002017Nausea and vomiting0GFM2 CL E G H8434029682ORPHA:565624Combined oxidative phosphorylation defect type 3943
HP:0002017HP:0002017Nausea and vomiting0GHSR CL E G H26934267ORPHA:314811Short stature due to GHSR deficiency37
HP:0002017HP:0002017Nausea and vomiting0GK CL E G H27104289OMIM:307030Glycerol kinase deficiency13
HP:0002017HP:0002017Nausea and vomiting0GLA CL E G H27174296ORPHA:324Fabry diseaseHP:0040282 - Frequent291
HP:0002017HP:0002017Nausea and vomiting0GLA CL E G H27174296OMIM:301500Fabry disease291
HP:0002017HP:0002017Nausea and vomiting0GLE1 CL E G H27334315ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional45
HP:0002017HP:0002017Nausea and vomiting0GLI2 CL E G H27364318ORPHA:93925Alobar holoprosencephaly173
HP:0002017HP:0002017Nausea and vomiting0GLI2 CL E G H27364318ORPHA:93924Lobar holoprosencephaly173
HP:0002017HP:0002017Nausea and vomiting0GLI2 CL E G H27364318ORPHA:93926Midline interhemispheric variant of holoprosencephaly173
HP:0002017HP:0002017Nausea and vomiting0GLI2 CL E G H27364318ORPHA:220386Semilobar holoprosencephaly173
HP:0002017HP:0002017Nausea and vomiting0GLT8D1 CL E G H5583024870ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0GRB10 CL E G H28874564ORPHA:96182Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
HP:0002017HP:0002017Nausea and vomiting0GTF2I CL E G H29694659ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0GTF2IRD1 CL E G H95694661ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0GTF2IRD2 CL E G H8416330775ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0HADH CL E G H30334799ORPHA:71212Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency41
HP:0002017HP:0002017Nausea and vomiting0HELLPAR CL E G H10110169243984ORPHA:244242HELLP syndrome
HP:0002017HP:0002017Nausea and vomiting0HFE CL E G H30774886OMIM:176200Porphyria variegata38
HP:0002017HP:0002017Nausea and vomiting0HIBCH CL E G H262754908ORPHA:88639Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency32
HP:0002017HP:0002017Nausea and vomiting0HLA-B CL E G H31064932ORPHA:117Behçet diseaseHP:0040281 - Very frequent4
HP:0002017HP:0002017Nausea and vomiting0HLA-B CL E G H31064932ORPHA:36426Stevens-Johnson syndromeHP:0040281 - Very frequent4
HP:0002017HP:0002017Nausea and vomiting0HLA-DPA1 CL E G H31134938ORPHA:900Granulomatosis with polyangiitisHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0HLA-DPB1 CL E G H31154940ORPHA:900Granulomatosis with polyangiitisHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0HLA-DQA1 CL E G H31174942OMIM:212750Celiac disease, susceptibility to, 1
HP:0002017HP:0002017Nausea and vomiting0HLA-DQB1 CL E G H31194944OMIM:212750Celiac disease, susceptibility to, 1
HP:0002017HP:0002017Nausea and vomiting0HLA-DRB1 CL E G H31234948ORPHA:220393Diffuse cutaneous systemic sclerosisHP:0040283 - Occasional2
HP:0002017HP:0002017Nausea and vomiting0HLA-DRB1 CL E G H31234948ORPHA:220402Limited cutaneous systemic sclerosisHP:0040282 - Frequent2
HP:0002017HP:0002017Nausea and vomiting0HLCS CL E G H31414976ORPHA:79242Holocarboxylase synthetase deficiencyHP:0040281 - Very frequent148
HP:0002017HP:0002017Nausea and vomiting0HLCS CL E G H31414976OMIM:253270Holocarboxylase synthetase deficiency148
HP:0002017HP:0002017Nausea and vomiting0HMBS CL E G H31454982ORPHA:79276Acute intermittent porphyriaHP:0040282 - Frequent81
HP:0002017HP:0002017Nausea and vomiting0HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent81
HP:0002017HP:0002017Nausea and vomiting0HMGCL CL E G H31555005ORPHA:203-hydroxy-3-methylglutaric aciduria35
HP:0002017HP:0002017Nausea and vomiting0HMGCL CL E G H31555005OMIM:2464503-Hydroxy-3-Methylglutaryl-Coa lyase deficiency35
HP:0002017HP:0002017Nausea and vomiting0HMGCS2 CL E G H31585008OMIM:6059113-Hydroxy-3-Methylglutaryl-Coa synthase-2 deficiency42
HP:0002017HP:0002017Nausea and vomiting0HNF4A CL E G H31725024ORPHA:263455Hyperinsulinism due to HNF4A deficiency138
HP:0002017HP:0002017Nausea and vomiting0HNRNPA1 CL E G H31785031ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional31
HP:0002017HP:0002017Nausea and vomiting0HNRNPK CL E G H31905044ORPHA:352665Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion8
HP:0002017HP:0002017Nausea and vomiting0HNRNPK CL E G H31905044ORPHA:453504Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation8
HP:0002017HP:0002017Nausea and vomiting0HPRT1 CL E G H32515157OMIM:300322Lesch-Nyhan syndrome76
HP:0002017HP:0002017Nausea and vomiting0HS3ST6 CL E G H6471114178OMIM:619367ANGIOEDEMA, HEREDITARY, 8; HAE8
HP:0002017HP:0002017Nausea and vomiting0HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency34
HP:0002017HP:0002017Nausea and vomiting0HTRA2 CL E G H2742914348ORPHA:2828Young-onset Parkinson disease39
HP:0002017HP:0002017Nausea and vomiting0IFNGR1 CL E G H34595439ORPHA:117Behçet diseaseHP:0040281 - Very frequent60
HP:0002017HP:0002017Nausea and vomiting0IGH CL E G H34925477ORPHA:52417MALT lymphomaHP:0040281 - Very frequent7
HP:0002017HP:0002017Nausea and vomiting0IKZF1 CL E G H1032013176ORPHA:36426Stevens-Johnson syndromeHP:0040281 - Very frequent8
HP:0002017HP:0002017Nausea and vomiting0IL10 CL E G H35865962ORPHA:117Behçet diseaseHP:0040281 - Very frequent2
HP:0002017HP:0002017Nausea and vomiting0IL12A CL E G H35925969ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0IL12A-AS1 CL E G H10192837649094ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0IL18BP CL E G H100685987OMIM:618549HEPATITIS, FULMINANT VIRAL, SUSCEPTIBILITY TO; FVH
HP:0002017HP:0002017Nausea and vomiting0IL23R CL E G H14923319100ORPHA:117Behçet diseaseHP:0040281 - Very frequent1
HP:0002017HP:0002017Nausea and vomiting0IRAK1 CL E G H36546112ORPHA:93552Pediatric systemic lupus erythematosus
HP:0002017HP:0002017Nausea and vomiting0IRF5 CL E G H36636120ORPHA:220393Diffuse cutaneous systemic sclerosisHP:0040283 - Occasional4
HP:0002017HP:0002017Nausea and vomiting0IRF5 CL E G H36636120ORPHA:220402Limited cutaneous systemic sclerosisHP:0040282 - Frequent4
HP:0002017HP:0002017Nausea and vomiting0ITGA6 CL E G H36556142ORPHA:79403Junctional epidermolysis bullosa with pyloric atresiaHP:0040281 - Very frequent79
HP:0002017HP:0002017Nausea and vomiting0ITGB4 CL E G H36916158ORPHA:158684Epidermolysis bullosa simplex with pyloric atresia124
HP:0002017HP:0002017Nausea and vomiting0ITGB4 CL E G H36916158ORPHA:79403Junctional epidermolysis bullosa with pyloric atresiaHP:0040281 - Very frequent124
HP:0002017HP:0002017Nausea and vomiting0IVD CL E G H37126186OMIM:243500Isovaleric acidemia105
HP:0002017HP:0002017Nausea and vomiting0KARS1 CL E G H37356215OMIM:619147LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS; LEPID
HP:0002017HP:0002017Nausea and vomiting0KCNA1 CL E G H37366218ORPHA:37612Episodic ataxia type 1145
HP:0002017HP:0002017Nausea and vomiting0KCNJ1 CL E G H37586255OMIM:241200Bartter syndrome, antenatal, type 251
HP:0002017HP:0002017Nausea and vomiting0KCNJ11 CL E G H37676257ORPHA:79134DEND syndrome127
HP:0002017HP:0002017Nausea and vomiting0KCNJ5 CL E G H37626266ORPHA:251274Familial hyperaldosteronism type III128
HP:0002017HP:0002017Nausea and vomiting0KIAA0319L CL E G H7993230071ORPHA:220402Limited cutaneous systemic sclerosisHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paraganglioma202
HP:0002017HP:0002017Nausea and vomiting0KIT CL E G H38156342ORPHA:79455Cutaneous mastocytoma327
HP:0002017HP:0002017Nausea and vomiting0KIT CL E G H38156342ORPHA:44890Gastrointestinal stromal tumorHP:0040282 - Frequent327
HP:0002017HP:0002017Nausea and vomiting0KIT CL E G H38156342ORPHA:98849Systemic mastocytosis with associated hematologic neoplasm327
HP:0002017HP:0002017Nausea and vomiting0KLRC4 CL E G H83026377ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0KMT2E CL E G H5590418541OMIM:618512O'donnell-Luria-Rodan syndrome1
HP:0002017HP:0002017Nausea and vomiting0KRAS CL E G H38456407ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional196
HP:0002017HP:0002017Nausea and vomiting0KRAS CL E G H38456407ORPHA:144Lynch syndromeHP:0040282 - Frequent196
HP:0002017HP:0002017Nausea and vomiting0KRIT1 CL E G H8891573ORPHA:221061Familial cerebral cavernous malformation92
HP:0002017HP:0002017Nausea and vomiting0KYNU CL E G H89426469OMIM:236800HYDROXYKYNURENINURIA5
HP:0002017HP:0002017Nausea and vomiting0LAMA3 CL E G H39096483ORPHA:79404Severe generalized junctional epidermolysis bullosa116
HP:0002017HP:0002017Nausea and vomiting0LAMB3 CL E G H39146490ORPHA:79404Severe generalized junctional epidermolysis bullosa167
HP:0002017HP:0002017Nausea and vomiting0LAMC2 CL E G H39186493ORPHA:79404Severe generalized junctional epidermolysis bullosa135
HP:0002017HP:0002017Nausea and vomiting0LBX1 CL E G H1066016960OMIM:619483CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3; CCHS3
HP:0002017HP:0002017Nausea and vomiting0LIG3 CL E G H39806600ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathy1
HP:0002017HP:0002017Nausea and vomiting0LIMK1 CL E G H39846613ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0LIPA CL E G H39886617ORPHA:75234Cholesteryl ester storage diseaseHP:0040282 - Frequent73
HP:0002017HP:0002017Nausea and vomiting0LIPA CL E G H39886617OMIM:278000Lysosomal acid lipase deficiency73
HP:0002017HP:0002017Nausea and vomiting0LIPA CL E G H39886617ORPHA:75233Wolman diseaseHP:0040281 - Very frequent73
HP:0002017HP:0002017Nausea and vomiting0LMOD1 CL E G H258026647ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0LPL CL E G H40236677OMIM:238600Type I hyperlipoproteinemia106
HP:0002017HP:0002017Nausea and vomiting0LRRK2 CL E G H12089218618ORPHA:2828Young-onset Parkinson disease221
HP:0002017HP:0002017Nausea and vomiting0MALT1 CL E G H108926819ORPHA:52417MALT lymphomaHP:0040281 - Very frequent6
HP:0002017HP:0002017Nausea and vomiting0MARS1 CL E G H41416898OMIM:615486Interstitial lung and liver disease
HP:0002017HP:0002017Nausea and vomiting0MATR3 CL E G H97826912ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional80
HP:0002017HP:0002017Nausea and vomiting0MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paraganglioma84
HP:0002017HP:0002017Nausea and vomiting0MC2R CL E G H41586930ORPHA:361Familial glucocorticoid deficiency94
HP:0002017HP:0002017Nausea and vomiting0MCCC1 CL E G H569226936OMIM:2102003-Methylcrotonyl-CoA carboxylase 1 deficiency81
HP:0002017HP:0002017Nausea and vomiting0MCCC2 CL E G H640876937OMIM:2102103-Methylcrotonyl-CoA carboxylase 2 deficiency77
HP:0002017HP:0002017Nausea and vomiting0MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paraganglioma4
HP:0002017HP:0002017Nausea and vomiting0MED12 CL E G H996811957OMIM:301068HARDIKAR SYNDROME; HDKR228
HP:0002017HP:0002017Nausea and vomiting0MEFV CL E G H42106998ORPHA:117Behçet diseaseHP:0040281 - Very frequent281
HP:0002017HP:0002017Nausea and vomiting0MEFV CL E G H42106998ORPHA:342Familial Mediterranean feverHP:0040281 - Very frequent281
HP:0002017HP:0002017Nausea and vomiting0MEFV CL E G H42106998OMIM:249100Familial Mediterranean fever, AR281
HP:0002017HP:0002017Nausea and vomiting0MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1462
HP:0002017HP:0002017Nausea and vomiting0MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040282 - Frequent462
HP:0002017HP:0002017Nausea and vomiting0MET CL E G H42337029ORPHA:33402Pediatric hepatocellular carcinoma375
HP:0002017HP:0002017Nausea and vomiting0METTL27 CL E G H15536819068ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0MGME1 CL E G H9266716205OMIM:615084Mitochondrial DNA depletion syndrome 1111
HP:0002017HP:0002017Nausea and vomiting0MGME1 CL E G H9266716205ORPHA:352447Progressive external ophthalmoplegia-myopathy-emaciation syndrome11
HP:0002017HP:0002017Nausea and vomiting0MLH1 CL E G H42927127ORPHA:144Lynch syndromeHP:0040282 - Frequent1819
HP:0002017HP:0002017Nausea and vomiting0MLH3 CL E G H270307128ORPHA:144Lynch syndromeHP:0040282 - Frequent131
HP:0002017HP:0002017Nausea and vomiting0MLXIPL CL E G H5108512744ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0MLYCD CL E G H234177150OMIM:248360Malonyl-CoA decarboxylase deficiency80
HP:0002017HP:0002017Nausea and vomiting0MMAA CL E G H16678518871OMIM:251100Methylmalonic aciduria, Cbla type113
HP:0002017HP:0002017Nausea and vomiting0MMAB CL E G H32662519331OMIM:251110Methylmalonic aciduria, Cblb type127
HP:0002017HP:0002017Nausea and vomiting0MMUT CL E G H45947526OMIM:251000Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency
HP:0002017HP:0002017Nausea and vomiting0MMUT CL E G H45947526ORPHA:79312Vitamin B12-unresponsive methylmalonic acidemia type mut-HP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0MMUT CL E G H45947526ORPHA:289916Vitamin B12-unresponsive methylmalonic acidemia type mut0HP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0MPI CL E G H43517216OMIM:602579Congenital disorder of glycosylation, type Ib51
HP:0002017HP:0002017Nausea and vomiting0MPI CL E G H43517216ORPHA:79319MPI-CDG51
HP:0002017HP:0002017Nausea and vomiting0MPV17 CL E G H43587224OMIM:256810Navajo neurohepatopathy56
HP:0002017HP:0002017Nausea and vomiting0MRAP CL E G H562461304ORPHA:361Familial glucocorticoid deficiency26
HP:0002017HP:0002017Nausea and vomiting0MRPS7 CL E G H5108114499OMIM:617872Combined oxidative phosphorylation deficiency 3412
HP:0002017HP:0002017Nausea and vomiting0MSH2 CL E G H44367325ORPHA:144Lynch syndromeHP:0040282 - Frequent2162
HP:0002017HP:0002017Nausea and vomiting0MSH6 CL E G H29567329ORPHA:144Lynch syndromeHP:0040282 - Frequent2232
HP:0002017HP:0002017Nausea and vomiting0MSX2 CL E G H44887392ORPHA:60015Enlarged parietal foramina45
HP:0002017HP:0002017Nausea and vomiting0MTHFD1 CL E G H45227432OMIM:617780Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia5
HP:0002017HP:0002017Nausea and vomiting0MTRR CL E G H45527473ORPHA:2169Methylcobalamin deficiency type cblE88
HP:0002017HP:0002017Nausea and vomiting0MTTP CL E G H45477467ORPHA:14Abetalipoproteinemia81
HP:0002017HP:0002017Nausea and vomiting0MVK CL E G H45987530OMIM:260920Hyper-Igd syndrome150
HP:0002017HP:0002017Nausea and vomiting0MVK CL E G H45987530OMIM:610377Mevalonic aciduria150
HP:0002017HP:0002017Nausea and vomiting0MYC CL E G H46097553ORPHA:543Burkitt lymphomaHP:0040283 - Occasional11
HP:0002017HP:0002017Nausea and vomiting0MYH11 CL E G H46297569ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent418
HP:0002017HP:0002017Nausea and vomiting0MYLK CL E G H46387590ORPHA:2241Megacystis-microcolon-intestinal hypoperistalsis syndromeHP:0040281 - Very frequent326
HP:0002017HP:0002017Nausea and vomiting0NAA10 CL E G H826018704OMIM:300855Ogden syndrome23
HP:0002017HP:0002017Nausea and vomiting0NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiency36
HP:0002017HP:0002017Nausea and vomiting0NAGS CL E G H16241717996OMIM:237310N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY36
HP:0002017HP:0002017Nausea and vomiting0NARS2 CL E G H7973126274ORPHA:79134DEND syndrome34
HP:0002017HP:0002017Nausea and vomiting0NAXD CL E G H5573925576OMIM:618321Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2
HP:0002017HP:0002017Nausea and vomiting0NBAS CL E G H5159415625OMIM:616483INFANTILE LIVER FAILURE SYNDROME 2; ILFS225
HP:0002017HP:0002017Nausea and vomiting0NCF1 CL E G H6533617660ORPHA:904Williams syndromeHP:0040282 - Frequent13
HP:0002017HP:0002017Nausea and vomiting0ND1 CL E G H45357455ORPHA:2609Isolated complex I deficiency
HP:0002017HP:0002017Nausea and vomiting0ND1 CL E G H45357455ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0ND1 CL E G H45357455ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0ND2 CL E G H45367456ORPHA:2609Isolated complex I deficiency
HP:0002017HP:0002017Nausea and vomiting0ND2 CL E G H45367456ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ND3 CL E G H45377458ORPHA:2609Isolated complex I deficiency
HP:0002017HP:0002017Nausea and vomiting0ND3 CL E G H45377458ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ND4 CL E G H45387459ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0ND4 CL E G H45387459ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ND5 CL E G H45407461ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0ND5 CL E G H45407461ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0ND6 CL E G H45417462ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0ND6 CL E G H45417462ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0NDUFA1 CL E G H46947683ORPHA:2609Isolated complex I deficiency7
HP:0002017HP:0002017Nausea and vomiting0NDUFA11 CL E G H12632820371ORPHA:2609Isolated complex I deficiency32
HP:0002017HP:0002017Nausea and vomiting0NDUFA6 CL E G H47007690ORPHA:2609Isolated complex I deficiency1
HP:0002017HP:0002017Nausea and vomiting0NDUFAF1 CL E G H5110318828ORPHA:2609Isolated complex I deficiency40
HP:0002017HP:0002017Nausea and vomiting0NDUFAF2 CL E G H9194228086ORPHA:2609Isolated complex I deficiency26
HP:0002017HP:0002017Nausea and vomiting0NDUFAF3 CL E G H2591529918ORPHA:2609Isolated complex I deficiency31
HP:0002017HP:0002017Nausea and vomiting0NDUFAF4 CL E G H2907821034ORPHA:2609Isolated complex I deficiency50
HP:0002017HP:0002017Nausea and vomiting0NDUFAF5 CL E G H7913315899ORPHA:2609Isolated complex I deficiency34
HP:0002017HP:0002017Nausea and vomiting0NDUFAF8 CL E G H28418433551ORPHA:2609Isolated complex I deficiency
HP:0002017HP:0002017Nausea and vomiting0NDUFB10 CL E G H47167696ORPHA:2609Isolated complex I deficiency
HP:0002017HP:0002017Nausea and vomiting0NDUFB11 CL E G H5453920372ORPHA:2609Isolated complex I deficiency3
HP:0002017HP:0002017Nausea and vomiting0NDUFB3 CL E G H47097698ORPHA:2609Isolated complex I deficiency9
HP:0002017HP:0002017Nausea and vomiting0NDUFB9 CL E G H47157704ORPHA:2609Isolated complex I deficiency16
HP:0002017HP:0002017Nausea and vomiting0NDUFS1 CL E G H47197707ORPHA:2609Isolated complex I deficiency81
HP:0002017HP:0002017Nausea and vomiting0NDUFS1 CL E G H47197707OMIM:618226Mitochondrial complex I deficiency, nuclear type 581
HP:0002017HP:0002017Nausea and vomiting0NDUFS2 CL E G H47207708ORPHA:2609Isolated complex I deficiency65
HP:0002017HP:0002017Nausea and vomiting0NDUFS3 CL E G H47227710ORPHA:2609Isolated complex I deficiency22
HP:0002017HP:0002017Nausea and vomiting0NDUFS4 CL E G H47247711ORPHA:2609Isolated complex I deficiency27
HP:0002017HP:0002017Nausea and vomiting0NDUFS4 CL E G H47247711OMIM:252010Mitochondrial complex I deficiency, nuclear type 127
HP:0002017HP:0002017Nausea and vomiting0NDUFS6 CL E G H47267713ORPHA:2609Isolated complex I deficiency21
HP:0002017HP:0002017Nausea and vomiting0NDUFS7 CL E G H3742917714ORPHA:2609Isolated complex I deficiency38
HP:0002017HP:0002017Nausea and vomiting0NDUFS8 CL E G H47287715ORPHA:2609Isolated complex I deficiency42
HP:0002017HP:0002017Nausea and vomiting0NDUFV1 CL E G H47237716ORPHA:2609Isolated complex I deficiency74
HP:0002017HP:0002017Nausea and vomiting0NDUFV1 CL E G H47237716OMIM:618225Mitochondrial complex I deficiency, nuclear type 474
HP:0002017HP:0002017Nausea and vomiting0NDUFV2 CL E G H47297717ORPHA:2609Isolated complex I deficiency27
HP:0002017HP:0002017Nausea and vomiting0NEFH CL E G H47447737ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional24
HP:0002017HP:0002017Nausea and vomiting0NEK1 CL E G H47507744ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional101
HP:0002017HP:0002017Nausea and vomiting0NEUROG3 CL E G H5067413806OMIM:610370Diarrhea 4, malabsorptive, congenital5
HP:0002017HP:0002017Nausea and vomiting0NEUROG3 CL E G H5067413806ORPHA:83620Enteric anendocrinosis5
HP:0002017HP:0002017Nausea and vomiting0NEXMIF CL E G H34053329433OMIM:300912Mental retardation, X-linked 9852
HP:0002017HP:0002017Nausea and vomiting0NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paraganglioma1952
HP:0002017HP:0002017Nausea and vomiting0NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040282 - Frequent220
HP:0002017HP:0002017Nausea and vomiting0NFIX CL E G H47847788ORPHA:44798019p13.3 microduplication syndrome40
HP:0002017HP:0002017Nausea and vomiting0NLRC4 CL E G H5848416412OMIM:616050AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC30
HP:0002017HP:0002017Nausea and vomiting0NLRP3 CL E G H11454816400ORPHA:1451CINCA syndromeHP:0040281 - Very frequent217
HP:0002017HP:0002017Nausea and vomiting0NLRP3 CL E G H11454816400ORPHA:47045Familial cold urticariaHP:0040282 - Frequent217
HP:0002017HP:0002017Nausea and vomiting0NNT CL E G H235307863ORPHA:361Familial glucocorticoid deficiency13
HP:0002017HP:0002017Nausea and vomiting0NODAL CL E G H48387865ORPHA:93925Alobar holoprosencephaly45
HP:0002017HP:0002017Nausea and vomiting0NODAL CL E G H48387865ORPHA:93924Lobar holoprosencephaly45
HP:0002017HP:0002017Nausea and vomiting0NODAL CL E G H48387865ORPHA:93926Midline interhemispheric variant of holoprosencephaly45
HP:0002017HP:0002017Nausea and vomiting0NODAL CL E G H48387865ORPHA:220386Semilobar holoprosencephaly45
HP:0002017HP:0002017Nausea and vomiting0NOTCH2NLC CL E G H10099671753924OMIM:603472NEURONAL INTRANUCLEAR INCLUSION DISEASE
HP:0002017HP:0002017Nausea and vomiting0NPPA CL E G H48787939ORPHA:1344Atrial standstill13
HP:0002017HP:0002017Nausea and vomiting0NR3C2 CL E G H43067979OMIM:177735Pseudohypoaldosteronism, type I, autosomal dominant109
HP:0002017HP:0002017Nausea and vomiting0NRTN CL E G H49028007ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent4
HP:0002017HP:0002017Nausea and vomiting0NSD1 CL E G H6432414234OMIM:117550Sotos syndrome 1544
HP:0002017HP:0002017Nausea and vomiting0NUBPL CL E G H8022420278ORPHA:2609Isolated complex I deficiency89
HP:0002017HP:0002017Nausea and vomiting0OPLAH CL E G H268738149OMIM:2600055-@oxoprolinase deficiency5
HP:0002017HP:0002017Nausea and vomiting0OPTN CL E G H1013317142ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional62
HP:0002017HP:0002017Nausea and vomiting0OTC CL E G H50098512OMIM:311250Ornithine transcarbamylase deficiency, hyperammonemia due to369
HP:0002017HP:0002017Nausea and vomiting0OXCT1 CL E G H50198527OMIM:245050Succinyl CoA:3-oxoacid CoA transferase deficiency52
HP:0002017HP:0002017Nausea and vomiting0PAH CL E G H50538582ORPHA:79254Classic phenylketonuriaHP:0040282 - Frequent641
HP:0002017HP:0002017Nausea and vomiting0PALB2 CL E G H7972826144ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional1349
HP:0002017HP:0002017Nausea and vomiting0PALLD CL E G H2302217068ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional192
HP:0002017HP:0002017Nausea and vomiting0PARK7 CL E G H1131516369ORPHA:2828Young-onset Parkinson disease23
HP:0002017HP:0002017Nausea and vomiting0PCCA CL E G H50958653OMIM:606054Propionic acidemia96
HP:0002017HP:0002017Nausea and vomiting0PCCB CL E G H50968654OMIM:606054Propionic acidemia92
HP:0002017HP:0002017Nausea and vomiting0PDCD10 CL E G H112358761ORPHA:221061Familial cerebral cavernous malformation21
HP:0002017HP:0002017Nausea and vomiting0PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040282 - Frequent9
HP:0002017HP:0002017Nausea and vomiting0PDGFRA CL E G H51568803ORPHA:44890Gastrointestinal stromal tumorHP:0040282 - Frequent337
HP:0002017HP:0002017Nausea and vomiting0PDSS2 CL E G H5710723041ORPHA:255249Leigh syndrome with nephrotic syndrome54
HP:0002017HP:0002017Nausea and vomiting0PERCC1 CL E G H10537104552293ORPHA:92050Congenital tufting enteropathy
HP:0002017HP:0002017Nausea and vomiting0PFN1 CL E G H52168881ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional6
HP:0002017HP:0002017Nausea and vomiting0PGM1 CL E G H52368905OMIM:614921Congenital disorder of glycosylation, type It58
HP:0002017HP:0002017Nausea and vomiting0PHGDH CL E G H262278923ORPHA:793513-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form37
HP:0002017HP:0002017Nausea and vomiting0PHKA2 CL E G H52568926ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiency54
HP:0002017HP:0002017Nausea and vomiting0PHKB CL E G H52578927ORPHA:79240Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency101
HP:0002017HP:0002017Nausea and vomiting0PHKG2 CL E G H52618931ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiency48
HP:0002017HP:0002017Nausea and vomiting0PIGY CL E G H8499228213OMIM:616809Hyperphosphatasia with mental retardation syndrome 62
HP:0002017HP:0002017Nausea and vomiting0PIK3CA CL E G H52908975ORPHA:144Lynch syndromeHP:0040282 - Frequent162
HP:0002017HP:0002017Nausea and vomiting0PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040282 - Frequent162
HP:0002017HP:0002017Nausea and vomiting0PINK1 CL E G H6501814581ORPHA:2828Young-onset Parkinson disease55
HP:0002017HP:0002017Nausea and vomiting0PKHD1 CL E G H53149016ORPHA:53035Caroli disease563
HP:0002017HP:0002017Nausea and vomiting0PLCH1 CL E G H2300729185ORPHA:93925Alobar holoprosencephaly
HP:0002017HP:0002017Nausea and vomiting0PLEC CL E G H53399069ORPHA:158684Epidermolysis bullosa simplex with pyloric atresia759
HP:0002017HP:0002017Nausea and vomiting0PMM2 CL E G H53739115OMIM:212065Congenital disorder of glycosylation, type Ia150
HP:0002017HP:0002017Nausea and vomiting0PMM2 CL E G H53739115ORPHA:79318PMM2-CDG150
HP:0002017HP:0002017Nausea and vomiting0PMS1 CL E G H53789121ORPHA:144Lynch syndromeHP:0040282 - Frequent56
HP:0002017HP:0002017Nausea and vomiting0PMS2 CL E G H53959122ORPHA:144Lynch syndromeHP:0040282 - Frequent1121
HP:0002017HP:0002017Nausea and vomiting0PNPLA8 CL E G H5064028900OMIM:251950Mitochondrial myopathy with lactic acidosis3
HP:0002017HP:0002017Nausea and vomiting0PNPT1 CL E G H8717823166OMIM:608703Spinocerebellar ataxia 2560
HP:0002017HP:0002017Nausea and vomiting0PNPT1 CL E G H8717823166ORPHA:101111Spinocerebellar ataxia type 2560
HP:0002017HP:0002017Nausea and vomiting0PODXL CL E G H54209171ORPHA:2828Young-onset Parkinson disease6
HP:0002017HP:0002017Nausea and vomiting0POLG CL E G H54289179OMIM:603041Mitochondrial DNA depletion syndrome 1 (mngie type)464
HP:0002017HP:0002017Nausea and vomiting0POLG CL E G H54289179OMIM:203700Mitochondrial DNA depletion syndrome 4A (Alpers type)464
HP:0002017HP:0002017Nausea and vomiting0POLG CL E G H54289179ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathy464
HP:0002017HP:0002017Nausea and vomiting0PON1 CL E G H54449204ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional4
HP:0002017HP:0002017Nausea and vomiting0PON2 CL E G H54459205ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional2
HP:0002017HP:0002017Nausea and vomiting0PON3 CL E G H54469206ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional1
HP:0002017HP:0002017Nausea and vomiting0PPARGC1A CL E G H108919237ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional1
HP:0002017HP:0002017Nausea and vomiting0PPM1D CL E G H84939277OMIM:617450Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold22
HP:0002017HP:0002017Nausea and vomiting0PPOX CL E G H54989280ORPHA:79473Porphyria variegata41
HP:0002017HP:0002017Nausea and vomiting0PPOX CL E G H54989280OMIM:176200Porphyria variegata41
HP:0002017HP:0002017Nausea and vomiting0PRKN CL E G H50718607ORPHA:2828Young-onset Parkinson disease138
HP:0002017HP:0002017Nausea and vomiting0PRPH CL E G H56309461ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional25
HP:0002017HP:0002017Nausea and vomiting0PRTN3 CL E G H56579495ORPHA:900Granulomatosis with polyangiitisHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0PSAP CL E G H56609498ORPHA:206436Infantile Krabbe disease81
HP:0002017HP:0002017Nausea and vomiting0PTCH1 CL E G H57279585ORPHA:93925Alobar holoprosencephaly665
HP:0002017HP:0002017Nausea and vomiting0PTCH1 CL E G H57279585ORPHA:93924Lobar holoprosencephaly665
HP:0002017HP:0002017Nausea and vomiting0PTCH1 CL E G H57279585ORPHA:93926Midline interhemispheric variant of holoprosencephaly665
HP:0002017HP:0002017Nausea and vomiting0PTCH1 CL E G H57279585ORPHA:220386Semilobar holoprosencephaly665
HP:0002017HP:0002017Nausea and vomiting0PTEN CL E G H57289588ORPHA:65285Lhermitte-Duclos diseaseHP:0040281 - Very frequent948
HP:0002017HP:0002017Nausea and vomiting0PTPN22 CL E G H261919652ORPHA:900Granulomatosis with polyangiitisHP:0040282 - Frequent3
HP:0002017HP:0002017Nausea and vomiting0PYCR2 CL E G H2992030262ORPHA:481152PYCR2-related microcephaly-progressive leukoencephalopathy11
HP:0002017HP:0002017Nausea and vomiting0RAB27A CL E G H58739766ORPHA:79477Griscelli syndrome type 2HP:0040283 - Occasional67
HP:0002017HP:0002017Nausea and vomiting0RABL3 CL E G H28528218072ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0RANBP2 CL E G H59039848ORPHA:88619Familial acute necrotizing encephalopathy57
HP:0002017HP:0002017Nausea and vomiting0RARS1 CL E G H59179870ORPHA:438114RARS-related autosomal recessive hypomyelinating leukodystrophy
HP:0002017HP:0002017Nausea and vomiting0RECQL4 CL E G H94019949ORPHA:221016Rothmund-Thomson syndrome type 2445
HP:0002017HP:0002017Nausea and vomiting0RELA CL E G H59709955ORPHA:251636Ependymoma1
HP:0002017HP:0002017Nausea and vomiting0RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paraganglioma572
HP:0002017HP:0002017Nausea and vomiting0RET CL E G H59799967ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent572
HP:0002017HP:0002017Nausea and vomiting0RET CL E G H59799967OMIM:142623Hirschsprung disease, susceptibility to, 1572
HP:0002017HP:0002017Nausea and vomiting0RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma572
HP:0002017HP:0002017Nausea and vomiting0RFC2 CL E G H59829970ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0RHBDF2 CL E G H7965120788ORPHA:2198Palmoplantar keratoderma-esophageal carcinoma syndromeHP:0040281 - Very frequent80
HP:0002017HP:0002017Nausea and vomiting0RNF6 CL E G H604910069ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040282 - Frequent3
HP:0002017HP:0002017Nausea and vomiting0RPS20 CL E G H622410405ORPHA:440437Familial colorectal cancer Type XHP:0040282 - Frequent1
HP:0002017HP:0002017Nausea and vomiting0RRM2B CL E G H5048417296OMIM:612075Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)125
HP:0002017HP:0002017Nausea and vomiting0RRM2B CL E G H5048417296ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathy125
HP:0002017HP:0002017Nausea and vomiting0RYR1 CL E G H626110483ORPHA:466650Exercise-induced malignant hyperthermia1200
HP:0002017HP:0002017Nausea and vomiting0SAA1 CL E G H628810513ORPHA:85445AA amyloidosis2
HP:0002017HP:0002017Nausea and vomiting0SAR1B CL E G H5112810535ORPHA:71Chylomicron retention disease8
HP:0002017HP:0002017Nausea and vomiting0SAR1B CL E G H5112810535OMIM:246700Chylomicron retention disease8
HP:0002017HP:0002017Nausea and vomiting0SCN2A CL E G H632610588OMIM:618924EPISODIC ATAXIA, TYPE 9; EA9427
HP:0002017HP:0002017Nausea and vomiting0SCN5A CL E G H633110593ORPHA:1344Atrial standstill1134
HP:0002017HP:0002017Nausea and vomiting0SCNN1A CL E G H633710599ORPHA:171876Generalized pseudohypoaldosteronism type 167
HP:0002017HP:0002017Nausea and vomiting0SCNN1A CL E G H633710599OMIM:264350Pseudohypoaldosteronism, type I, autosomal recessive67
HP:0002017HP:0002017Nausea and vomiting0SCNN1B CL E G H633810600ORPHA:171876Generalized pseudohypoaldosteronism type 161
HP:0002017HP:0002017Nausea and vomiting0SCNN1G CL E G H634010602ORPHA:171876Generalized pseudohypoaldosteronism type 157
HP:0002017HP:0002017Nausea and vomiting0SDHA CL E G H638910680ORPHA:44890Gastrointestinal stromal tumorHP:0040282 - Frequent304
HP:0002017HP:0002017Nausea and vomiting0SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paraganglioma304
HP:0002017HP:0002017Nausea and vomiting0SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paraganglioma55
HP:0002017HP:0002017Nausea and vomiting0SDHB CL E G H639010681ORPHA:44890Gastrointestinal stromal tumorHP:0040282 - Frequent237
HP:0002017HP:0002017Nausea and vomiting0SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paraganglioma237
HP:0002017HP:0002017Nausea and vomiting0SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma237
HP:0002017HP:0002017Nausea and vomiting0SDHC CL E G H639110682ORPHA:44890Gastrointestinal stromal tumorHP:0040282 - Frequent147
HP:0002017HP:0002017Nausea and vomiting0SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paraganglioma147
HP:0002017HP:0002017Nausea and vomiting0SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040283 - Occasional129
HP:0002017HP:0002017Nausea and vomiting0SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paraganglioma129
HP:0002017HP:0002017Nausea and vomiting0SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma129
HP:0002017HP:0002017Nausea and vomiting0SEMA3C CL E G H1051210725ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent1
HP:0002017HP:0002017Nausea and vomiting0SEMA3D CL E G H22311710726ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent2
HP:0002017HP:0002017Nausea and vomiting0SEMA4A CL E G H6421810729ORPHA:440437Familial colorectal cancer Type XHP:0040282 - Frequent48
HP:0002017HP:0002017Nausea and vomiting0SERPING1 CL E G H7101228OMIM:106100Angioedema, hereditary, 164
HP:0002017HP:0002017Nausea and vomiting0SERPING1 CL E G H7101228ORPHA:100050Hereditary angioedema type 164
HP:0002017HP:0002017Nausea and vomiting0SHANK3 CL E G H8535814294ORPHA:48652Monosomy 22q13.3HP:0040283 - Occasional53
HP:0002017HP:0002017Nausea and vomiting0SHANK3 CL E G H8535814294OMIM:606232Phelan-Mcdermid syndrome53
HP:0002017HP:0002017Nausea and vomiting0SHH CL E G H646910848ORPHA:93925Alobar holoprosencephaly67
HP:0002017HP:0002017Nausea and vomiting0SHH CL E G H646910848ORPHA:93924Lobar holoprosencephaly67
HP:0002017HP:0002017Nausea and vomiting0SHH CL E G H646910848ORPHA:93926Midline interhemispheric variant of holoprosencephaly67
HP:0002017HP:0002017Nausea and vomiting0SHH CL E G H646910848ORPHA:220386Semilobar holoprosencephaly67
HP:0002017HP:0002017Nausea and vomiting0SI CL E G H647610856ORPHA:35122Congenital sucrase-isomaltase deficiency98
HP:0002017HP:0002017Nausea and vomiting0SIX3 CL E G H649610889ORPHA:93925Alobar holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0SIX3 CL E G H649610889ORPHA:93924Lobar holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0SIX3 CL E G H649610889ORPHA:93926Midline interhemispheric variant of holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0SIX3 CL E G H649610889ORPHA:220386Semilobar holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0SLC12A1 CL E G H655710910OMIM:601678Bartter syndrome, type 1, antenatal75
HP:0002017HP:0002017Nausea and vomiting0SLC12A3 CL E G H655910912OMIM:263800Gitelman syndrome145
HP:0002017HP:0002017Nausea and vomiting0SLC12A3 CL E G H655910912ORPHA:358Gitelman syndromeHP:0040283 - Occasional145
HP:0002017HP:0002017Nausea and vomiting0SLC19A3 CL E G H8070416266OMIM:607483Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)110
HP:0002017HP:0002017Nausea and vomiting0SLC1A3 CL E G H650710941ORPHA:2131Alternating hemiplegia of childhood63
HP:0002017HP:0002017Nausea and vomiting0SLC1A3 CL E G H650710941ORPHA:209967Episodic ataxia type 6HP:0040281 - Very frequent63
HP:0002017HP:0002017Nausea and vomiting0SLC1A3 CL E G H650710941OMIM:612656Episodic ataxia, type 663
HP:0002017HP:0002017Nausea and vomiting0SLC22A12 CL E G H11608517989ORPHA:94088Hereditary renal hypouricemia56
HP:0002017HP:0002017Nausea and vomiting0SLC22A5 CL E G H658410969OMIM:212140Carnitine deficiency, systemic primary207
HP:0002017HP:0002017Nausea and vomiting0SLC22A5 CL E G H658410969ORPHA:158Systemic primary carnitine deficiency207
HP:0002017HP:0002017Nausea and vomiting0SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paraganglioma
HP:0002017HP:0002017Nausea and vomiting0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type II82
HP:0002017HP:0002017Nausea and vomiting0SLC25A15 CL E G H1016610985ORPHA:415Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome88
HP:0002017HP:0002017Nausea and vomiting0SLC25A15 CL E G H1016610985OMIM:238970Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome88
HP:0002017HP:0002017Nausea and vomiting0SLC25A4 CL E G H29110990OMIM:615418Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)68
HP:0002017HP:0002017Nausea and vomiting0SLC2A9 CL E G H5660613446ORPHA:94088Hereditary renal hypouricemia57
HP:0002017HP:0002017Nausea and vomiting0SLC37A4 CL E G H25424061OMIM:619525CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw; CDG2W110
HP:0002017HP:0002017Nausea and vomiting0SLC46A1 CL E G H11323530521ORPHA:90045Hereditary folate malabsorptionHP:0040281 - Very frequent101
HP:0002017HP:0002017Nausea and vomiting0SLC5A1 CL E G H652311036ORPHA:35710Glucose-galactose malabsorption74
HP:0002017HP:0002017Nausea and vomiting0SLC5A6 CL E G H888411041OMIM:618973NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE; NERIB
HP:0002017HP:0002017Nausea and vomiting0SLC6A8 CL E G H653511055OMIM:300352Creatine deficiency syndrome, X-linked122
HP:0002017HP:0002017Nausea and vomiting0SLC7A7 CL E G H905611065OMIM:222700Lysinuric protein intolerance104
HP:0002017HP:0002017Nausea and vomiting0SLC7A7 CL E G H905611065ORPHA:470Lysinuric protein intolerance104
HP:0002017HP:0002017Nausea and vomiting0SMAD4 CL E G H40896770ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional504
HP:0002017HP:0002017Nausea and vomiting0SMARCB1 CL E G H659811103ORPHA:99966Atypical teratoid rhabdoid tumorHP:0040281 - Very frequent87
HP:0002017HP:0002017Nausea and vomiting0SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040282 - Frequent87
HP:0002017HP:0002017Nausea and vomiting0SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040282 - Frequent47
HP:0002017HP:0002017Nausea and vomiting0SMC1A CL E G H824311111ORPHA:220386Semilobar holoprosencephaly135
HP:0002017HP:0002017Nausea and vomiting0SMO CL E G H660811119ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent22
HP:0002017HP:0002017Nausea and vomiting0SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040282 - Frequent22
HP:0002017HP:0002017Nausea and vomiting0SMPD1 CL E G H660911120OMIM:257200Niemann-Pick disease, type A164
HP:0002017HP:0002017Nausea and vomiting0SNCA CL E G H662211138ORPHA:2828Young-onset Parkinson disease65
HP:0002017HP:0002017Nausea and vomiting0SOD1 CL E G H664711179ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional53
HP:0002017HP:0002017Nausea and vomiting0SPINK1 CL E G H669011244ORPHA:103918Tropical pancreatitis34
HP:0002017HP:0002017Nausea and vomiting0SPP1 CL E G H669611255ORPHA:93552Pediatric systemic lupus erythematosus
HP:0002017HP:0002017Nausea and vomiting0SPTBN1 CL E G H671111275OMIM:619475DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA
HP:0002017HP:0002017Nausea and vomiting0SQSTM1 CL E G H887811280ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional62
HP:0002017HP:0002017Nausea and vomiting0SREBF1 CL E G H672011289ORPHA:388Hirschsprung diseaseHP:0040281 - Very frequent1
HP:0002017HP:0002017Nausea and vomiting0SRSF2 CL E G H642710783ORPHA:98849Systemic mastocytosis with associated hematologic neoplasm1
HP:0002017HP:0002017Nausea and vomiting0SSR4 CL E G H674811326ORPHA:370927SSR4-CDG12
HP:0002017HP:0002017Nausea and vomiting0ST3GAL5 CL E G H886910872OMIM:609056Salt and pepper developmental regression syndrome47
HP:0002017HP:0002017Nausea and vomiting0STAG2 CL E G H1073511355ORPHA:93925Alobar holoprosencephaly1
HP:0002017HP:0002017Nausea and vomiting0STAG2 CL E G H1073511355ORPHA:220386Semilobar holoprosencephaly1
HP:0002017HP:0002017Nausea and vomiting0STAR CL E G H677011359ORPHA:361Familial glucocorticoid deficiency45
HP:0002017HP:0002017Nausea and vomiting0STAT4 CL E G H677511365ORPHA:117Behçet diseaseHP:0040281 - Very frequent2
HP:0002017HP:0002017Nausea and vomiting0STAT4 CL E G H677511365ORPHA:93552Pediatric systemic lupus erythematosus2
HP:0002017HP:0002017Nausea and vomiting0STIL CL E G H649110879ORPHA:93925Alobar holoprosencephaly99
HP:0002017HP:0002017Nausea and vomiting0STIL CL E G H649110879ORPHA:93924Lobar holoprosencephaly99
HP:0002017HP:0002017Nausea and vomiting0STIL CL E G H649110879ORPHA:93926Midline interhemispheric variant of holoprosencephaly99
HP:0002017HP:0002017Nausea and vomiting0STIL CL E G H649110879ORPHA:220386Semilobar holoprosencephaly99
HP:0002017HP:0002017Nausea and vomiting0STK11 CL E G H679411389ORPHA:2869Peutz-Jeghers syndrome740
HP:0002017HP:0002017Nausea and vomiting0STX1A CL E G H680411433ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0STX3 CL E G H680911438OMIM:619445DIARRHEA 12, WITH MICROVILLUS ATROPHY; DIAR121
HP:0002017HP:0002017Nausea and vomiting0SUCLG1 CL E G H880211449ORPHA:17Fatal infantile lactic acidosis with methylmalonic aciduria60
HP:0002017HP:0002017Nausea and vomiting0SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040282 - Frequent124
HP:0002017HP:0002017Nausea and vomiting0SUGCT CL E G H7978316001OMIM:231690Glutaric aciduria III8
HP:0002017HP:0002017Nausea and vomiting0SUOX CL E G H682111460OMIM:272300SULFOCYSTEINURIA40
HP:0002017HP:0002017Nausea and vomiting0SYK CL E G H685011491OMIM:619381IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION; IMD821
HP:0002017HP:0002017Nausea and vomiting0SYNJ1 CL E G H886711503ORPHA:2828Young-onset Parkinson disease9
HP:0002017HP:0002017Nausea and vomiting0SYT1 CL E G H685711509ORPHA:522077Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome1
HP:0002017HP:0002017Nausea and vomiting0TAF15 CL E G H814811547ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional
HP:0002017HP:0002017Nausea and vomiting0TARDBP CL E G H2343511571ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional65
HP:0002017HP:0002017Nausea and vomiting0TBK1 CL E G H2911011584ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional20
HP:0002017HP:0002017Nausea and vomiting0TBK1 CL E G H2911011584ORPHA:1930Herpes simplex virus encephalitisHP:0040282 - Frequent20
HP:0002017HP:0002017Nausea and vomiting0TBL2 CL E G H2660811586ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0TCN2 CL E G H694811653OMIM:275350Transcobalamin II deficiency57
HP:0002017HP:0002017Nausea and vomiting0TDGF1 CL E G H699711701ORPHA:93925Alobar holoprosencephaly1
HP:0002017HP:0002017Nausea and vomiting0TDGF1 CL E G H699711701ORPHA:93924Lobar holoprosencephaly1
HP:0002017HP:0002017Nausea and vomiting0TDGF1 CL E G H699711701ORPHA:93926Midline interhemispheric variant of holoprosencephaly1
HP:0002017HP:0002017Nausea and vomiting0TDGF1 CL E G H699711701ORPHA:220386Semilobar holoprosencephaly1
HP:0002017HP:0002017Nausea and vomiting0TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040282 - Frequent238
HP:0002017HP:0002017Nausea and vomiting0TET2 CL E G H5479025941ORPHA:98849Systemic mastocytosis with associated hematologic neoplasm3
HP:0002017HP:0002017Nausea and vomiting0TGFBR2 CL E G H704811773ORPHA:144Lynch syndromeHP:0040282 - Frequent253
HP:0002017HP:0002017Nausea and vomiting0TGFBR2 CL E G H704811773ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040282 - Frequent253
HP:0002017HP:0002017Nausea and vomiting0TGIF1 CL E G H705011776ORPHA:93925Alobar holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0TGIF1 CL E G H705011776ORPHA:93924Lobar holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0TGIF1 CL E G H705011776ORPHA:93926Midline interhemispheric variant of holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0TGIF1 CL E G H705011776ORPHA:220386Semilobar holoprosencephaly32
HP:0002017HP:0002017Nausea and vomiting0TICAM1 CL E G H14802218348ORPHA:1930Herpes simplex virus encephalitisHP:0040282 - Frequent6
HP:0002017HP:0002017Nausea and vomiting0TIMM22 CL E G H2992817317OMIM:618851COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43; COXPD43
HP:0002017HP:0002017Nausea and vomiting0TIMMDC1 CL E G H513001321ORPHA:2609Isolated complex I deficiency1
HP:0002017HP:0002017Nausea and vomiting0TLR3 CL E G H709811849ORPHA:1930Herpes simplex virus encephalitisHP:0040282 - Frequent3
HP:0002017HP:0002017Nausea and vomiting0TLR4 CL E G H709911850ORPHA:117Behçet diseaseHP:0040281 - Very frequent3
HP:0002017HP:0002017Nausea and vomiting0TMEM126B CL E G H5586330883ORPHA:2609Isolated complex I deficiency4
HP:0002017HP:0002017Nausea and vomiting0TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paraganglioma131
HP:0002017HP:0002017Nausea and vomiting0TMEM270 CL E G H13588623018ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 17
HP:0002017HP:0002017Nausea and vomiting0TNFRSF1A CL E G H713211916OMIM:142680Periodic fever, familial, autosomal dominant131
HP:0002017HP:0002017Nausea and vomiting0TNFRSF1A CL E G H713211916ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndrome131
HP:0002017HP:0002017Nausea and vomiting0TOM1 CL E G H1004311982OMIM:619510IMMUNODEFICIENCY 85 AND AUTOIMMUNITY; IMD85
HP:0002017HP:0002017Nausea and vomiting0TP53 CL E G H715711998ORPHA:1333Familial pancreatic carcinomaHP:0040283 - Occasional911
HP:0002017HP:0002017Nausea and vomiting0TP53 CL E G H715711998OMIM:260500Papilloma of choroid plexus911
HP:0002017HP:0002017Nausea and vomiting0TRAF3 CL E G H718712033ORPHA:1930Herpes simplex virus encephalitisHP:0040282 - Frequent2
HP:0002017HP:0002017Nausea and vomiting0TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0TREH CL E G H1118112266ORPHA:103909Trehalase deficiency2
HP:0002017HP:0002017Nausea and vomiting0TREM2 CL E G H5420917761ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional31
HP:0002017HP:0002017Nausea and vomiting0TRMT5 CL E G H5757023141OMIM:616539Combined oxidative phosphorylation deficiency 264
HP:0002017HP:0002017Nausea and vomiting0TRMU CL E G H5568725481OMIM:613070Liver failure, infantile, transient101
HP:0002017HP:0002017Nausea and vomiting0TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNF CL E G H45587481ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNH CL E G H45647487ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNK CL E G H45667489ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNL1 CL E G H45677490ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNL1 CL E G H45677490ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNQ CL E G H45727495ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNS1 CL E G H45747497ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNS2 CL E G H45757498ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNV CL E G H45777500ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TRNW CL E G H45787501ORPHA:550MELAS
HP:0002017HP:0002017Nausea and vomiting0TRNW CL E G H45787501ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002017Nausea and vomiting0TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002017Nausea and vomiting0TXNRD2 CL E G H1058718155ORPHA:361Familial glucocorticoid deficiency85
HP:0002017HP:0002017Nausea and vomiting0TYMP CL E G H18903148OMIM:603041Mitochondrial DNA depletion syndrome 1 (mngie type)138
HP:0002017HP:0002017Nausea and vomiting0TYMP CL E G H18903148ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathy138
HP:0002017HP:0002017Nausea and vomiting0UBAC2 CL E G H33786720486ORPHA:117Behçet diseaseHP:0040281 - Very frequent
HP:0002017HP:0002017Nausea and vomiting0UBQLN2 CL E G H2997812509ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional20
HP:0002017HP:0002017Nausea and vomiting0UCHL1 CL E G H734512513ORPHA:2828Young-onset Parkinson disease21
HP:0002017HP:0002017Nausea and vomiting0UNC13A CL E G H2302523150ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional1
HP:0002017HP:0002017Nausea and vomiting0UNC45A CL E G H5589830594OMIM:619377OSTEOOTOHEPATOENTERIC SYNDROME; OOHE
HP:0002017HP:0002017Nausea and vomiting0UNC93B1 CL E G H8162213481ORPHA:1930Herpes simplex virus encephalitisHP:0040282 - Frequent5
HP:0002017HP:0002017Nausea and vomiting0UQCC2 CL E G H8430021237OMIM:615824Mitochondrial complex III deficiency, nuclear type 77
HP:0002017HP:0002017Nausea and vomiting0UQCRC2 CL E G H738512586OMIM:615160Mitochondrial complex III deficiency, nuclear type 517
HP:0002017HP:0002017Nausea and vomiting0VAPB CL E G H921712649ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional116
HP:0002017HP:0002017Nausea and vomiting0VCP CL E G H741512666ORPHA:803Amyotrophic lateral sclerosisHP:0040283 - Occasional63
HP:0002017HP:0002017Nausea and vomiting0VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paraganglioma490
HP:0002017HP:0002017Nausea and vomiting0VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma490
HP:0002017HP:0002017Nausea and vomiting0VPS13C CL E G H5483223594ORPHA:2828Young-onset Parkinson disease8
HP:0002017HP:0002017Nausea and vomiting0VPS37D CL E G H15538218287ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0002017HP:0002017Nausea and vomiting0WT1 CL E G H749012796ORPHA:83469Desmoplastic small round cell tumorHP:0040282 - Frequent177
HP:0002017HP:0002017Nausea and vomiting0WWOX CL E G H5174112799ORPHA:99977Squamous cell carcinoma of the esophagusHP:0040282 - Frequent149
HP:0002017HP:0002017Nausea and vomiting0YARS1 CL E G H856512840OMIM:619418NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2; IMNEPD2
HP:0002017HP:0002017Nausea and vomiting0ZEB2 CL E G H983914881OMIM:235730Mowat-Wilson syndrome362
HP:0002017HP:0002017Nausea and vomiting0ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutation362
HP:0002017HP:0002017Nausea and vomiting0ZEB2 CL E G H983914881ORPHA:261537Mowat-Wilson syndrome due to monosomy 2q22362
HP:0002017HP:0002017Nausea and vomiting0ZFTA CL E G H6599828449ORPHA:251636Ependymoma
HP:0002017HP:0002017Nausea and vomiting0ZIC2 CL E G H754612873ORPHA:93925Alobar holoprosencephaly34
HP:0002017HP:0002017Nausea and vomiting0ZIC2 CL E G H754612873ORPHA:93924Lobar holoprosencephaly34
HP:0002017HP:0002017Nausea and vomiting0ZIC2 CL E G H754612873ORPHA:93926Midline interhemispheric variant of holoprosencephaly34
HP:0002017HP:0002017Nausea and vomiting0ZIC2 CL E G H754612873ORPHA:220386Semilobar holoprosencephaly34
HP:0002017HP:0002013Vomiting1AASS CL E G H1015717366ORPHA:2203HyperlysinemiaHP:0040283 - Occasional15
HP:0002017HP:0002013Vomiting1ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancyHP:0040283 - Occasional415
HP:0002017HP:0002013Vomiting1ABCC8 CL E G H683359ORPHA:79134DEND syndromeHP:0040283 - Occasional245
HP:0002017HP:0002013Vomiting1ACAD8 CL E G H2703487ORPHA:79159Isobutyryl-CoA dehydrogenase deficiencyHP:0040283 - Occasional58
HP:0002017HP:0002013Vomiting1ACADM CL E G H3489OMIM:201450Acyl-Coa dehydrogenase, medium-chain, deficiency of.197
HP:0002017HP:0002013Vomiting1ACADM CL E G H3489ORPHA:42Medium chain acyl-CoA dehydrogenase deficiencyHP:0040282 - Frequent197
HP:0002017HP:0002013Vomiting1ACADVL CL E G H3792ORPHA:26793Very long chain acyl-CoA dehydrogenase deficiencyHP:0040284 - Very rare200
HP:0002017HP:0002013Vomiting1ACADVL CL E G H3792OMIM:201475Very long-chain acyl-CoA dehydrogenase deficiency200
HP:0002017HP:0002013Vomiting1ACAT1 CL E G H3893OMIM:203750Alpha-Methylacetoacetic aciduria.91
HP:0002017HP:0002013Vomiting1ACAT1 CL E G H3893ORPHA:134Beta-ketothiolase deficiencyHP:0040281 - Very frequent91
HP:0002017HP:0002013Vomiting1ACSF3 CL E G H19732227288ORPHA:289504Combined malonic and methylmalonic acidemiaHP:0040283 - Occasional68
HP:0002017HP:0002013Vomiting1ACSF3 CL E G H19732227288OMIM:614265Combined malonic and methylmalonic aciduria.68
HP:0002017HP:0002013Vomiting1ACTG2 CL E G H72145OMIM:155310Visceral myopathy 1.23
HP:0002017HP:0002013Vomiting1ACY1 CL E G H95177ORPHA:137754Neurological conditions associated with aminoacylase 1 deficiencyHP:0040283 - Occasional13
HP:0002017HP:0002013Vomiting1ADNP CL E G H2339415766ORPHA:404448ADNP syndromeHP:0040283 - Occasional47
HP:0002017HP:0002013Vomiting1AIMP1 CL E G H925510648OMIM:260600Leukodystrophy, hypomyelinating, 34
HP:0002017HP:0002013Vomiting1AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040282 - Frequent95
HP:0002017HP:0002013Vomiting1ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiency62
HP:0002017HP:0002018Nausea1ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiencyHP:0040283 - Occasional62
HP:0002017HP:0002013Vomiting1ALAD CL E G H210395OMIM:612740Porphyria, acute hepatic.62
HP:0002017HP:0002013Vomiting1ALDH18A1 CL E G H58329722ORPHA:90348Autosomal dominant cutis laxa89
HP:0002017HP:0002013Vomiting1ALDH18A1 CL E G H58329722OMIM:601162Spastic paraplegia 9A, autosomal dominant.89
HP:0002017HP:0002013Vomiting1ALDOB CL E G H229417OMIM:229600Fructose intolerance, hereditary.73
HP:0002017HP:0002018Nausea1ALDOB CL E G H229417OMIM:229600Fructose intolerance, hereditary.73
HP:0002017HP:0002013Vomiting1ALDOB CL E G H229417ORPHA:469Hereditary fructose intoleranceHP:0040283 - Occasional73
HP:0002017HP:0002018Nausea1ALDOB CL E G H229417ORPHA:469Hereditary fructose intoleranceHP:0040282 - Frequent73
HP:0002017HP:0002013Vomiting1ALG11 CL E G H44013832456ORPHA:280071ALG11-CDG41
HP:0002017HP:0002013Vomiting1ALG11 CL E G H44013832456OMIM:613661Congenital disorder of glycosylation, type Ip.41
HP:0002017HP:0002013Vomiting1ALG3 CL E G H1019523056OMIM:601110Congenital disorder of glycosylation, type Id.37
HP:0002017HP:0002013Vomiting1ALG8 CL E G H7905323161ORPHA:79325ALG8-CDGHP:0040283 - Occasional46
HP:0002017HP:0002013Vomiting1ALG8 CL E G H7905323161OMIM:608104Congenital disorder of glycosylation, type Ih.46
HP:0002017HP:0002013Vomiting1ALG9 CL E G H7979615672ORPHA:79328ALG9-CDGHP:0040283 - Occasional93
HP:0002017HP:0002013Vomiting1ALPL CL E G H249438OMIM:241500Hypophosphatasia, infantile.126
HP:0002017HP:0002013Vomiting1ALX4 CL E G H60529450ORPHA:60015Enlarged parietal foraminaHP:0040283 - Occasional132
HP:0002017HP:0002013Vomiting1AMN CL E G H8169314604ORPHA:35858Imerslund-Gräsbeck syndromeHP:0040283 - Occasional25
HP:0002017HP:0002013Vomiting1ANAPC1 CL E G H6468219988ORPHA:221008Rothmund-Thomson syndrome type 1HP:0040283 - Occasional2
HP:0002017HP:0002013Vomiting1ANO1 CL E G H5510721625OMIM:620045
HP:0002017HP:0002018Nausea1APC CL E G H324583ORPHA:99818Turcot syndrome with polyposisHP:0040283 - Occasional3179
HP:0002017HP:0002013Vomiting1APC CL E G H324583ORPHA:99818Turcot syndrome with polyposisHP:0040283 - Occasional3179
HP:0002017HP:0002013Vomiting1AQP2 CL E G H359634OMIM:125800Diabetes insipidus, nephrogenic, 2.75
HP:0002017HP:0002013Vomiting1ARG1 CL E G H383663OMIM:207800Argininemia.31
HP:0002017HP:0002013Vomiting1ASL CL E G H435746OMIM:207900Argininosuccinic aciduria.81
HP:0002017HP:0002013Vomiting1ASPA CL E G H443756ORPHA:314911Severe Canavan diseaseHP:0040282 - Frequent48
HP:0002017HP:0002013Vomiting1ASS1 CL E G H445758OMIM:215700Citrullinemia, classic.119
HP:0002017HP:0002013Vomiting1ASXL1 CL E G H17102318318ORPHA:97297Bohring-Opitz syndromeHP:0040282 - Frequent145
HP:0002017HP:0002018Nausea1ASXL1 CL E G H17102318318ORPHA:98849Systemic mastocytosis with associated hematologic neoplasmHP:0040283 - Occasional145
HP:0002017HP:0002013Vomiting1ASXL3 CL E G H8081629357OMIM:615485BAINBRIDGE-ROPERS SYNDROME; BRPS49
HP:0002017HP:0002013Vomiting1ATP1A2 CL E G H477800ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent239
HP:0002017HP:0002018Nausea1ATP1A2 CL E G H477800OMIM:602481Migraine, familial hemiplegic, 2239
HP:0002017HP:0002013Vomiting1ATP1A3 CL E G H478801ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent150
HP:0002017HP:0002013Vomiting1ATP6 CL E G H45087414ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ATP6V0A4 CL E G H50617866OMIM:602722RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR64
HP:0002017HP:0002013Vomiting1ATP7B CL E G H540870OMIM:277900Wilson disease315
HP:0002017HP:0002013Vomiting1ATRX CL E G H546886OMIM:309580Mental retardation-hypotonic facies syndrome, X-linked, 1.169
HP:0002017HP:0002013Vomiting1AVP CL E G H551894ORPHA:30925Hereditary central diabetes insipidusHP:0040282 - Frequent22
HP:0002017HP:0002013Vomiting1AVPR2 CL E G H554897OMIM:304800Diabetes insipidus, nephrogenic, X-linked.67
HP:0002017HP:0002013Vomiting1BCKDHA CL E G H593986OMIM:248600Maple syrup urine disease.120
HP:0002017HP:0002013Vomiting1BCKDHB CL E G H594987OMIM:248600Maple syrup urine disease.162
HP:0002017HP:0002013Vomiting1BOLA3 CL E G H38896224415OMIM:614299Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia.14
HP:0002017HP:0002013Vomiting1BRAF CL E G H6731097OMIM:115150Cardiofaciocutaneous syndrome 1.276
HP:0002017HP:0002013Vomiting1BSND CL E G H780916512ORPHA:89938Infantile Bartter syndrome with sensorineural deafnessHP:0040283 - Occasional53
HP:0002017HP:0002013Vomiting1BTD CL E G H6861122OMIM:253260Biotinidase deficiencymultiple carboxylase deficiency, late-onset.223
HP:0002017HP:0002013Vomiting1CACNA1A CL E G H7731388ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent449
HP:0002017HP:0002013Vomiting1CACNA1A CL E G H7731388ORPHA:71518Benign paroxysmal torticollis of infancyHP:0040282 - Frequent449
HP:0002017HP:0002018Nausea1CACNA1D CL E G H7761391ORPHA:369929Primary hyperaldosteronism-seizures-neurological abnormalities syndromeHP:0040283 - Occasional51
HP:0002017HP:0002013Vomiting1CARD8 CL E G H2290017057OMIM:619079INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 30; IBD301
HP:0002017HP:0002013Vomiting1CAV1 CL E G H8571527OMIM:606721Lipodystrophy, familial partial, type 711
HP:0002017HP:0002013Vomiting1CCM2 CL E G H8360521708ORPHA:221061Familial cerebral cavernous malformation37
HP:0002017HP:0002013Vomiting1CD46 CL E G H41796953ORPHA:244242HELLP syndromeHP:0040283 - Occasional39
HP:0002017HP:0002018Nausea1CD46 CL E G H41796953ORPHA:244242HELLP syndromeHP:0040283 - Occasional39
HP:0002017HP:0002013Vomiting1CD55 CL E G H16042665OMIM:226300Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy.9
HP:0002017HP:0002013Vomiting1CDC42BPB CL E G H95781738OMIM:619841
HP:0002017HP:0002013Vomiting1CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040282 - Frequent636
HP:0002017HP:0002013Vomiting1CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040282 - Frequent636
HP:0002017HP:0002013Vomiting1CDK13 CL E G H86211733OMIM:617360Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder8
HP:0002017HP:0002013Vomiting1CDK8 CL E G H10241779OMIM:618748INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA
HP:0002017HP:0002013Vomiting1CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional2
HP:0002017HP:0002018Nausea1CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional2
HP:0002017HP:0002018Nausea1CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional102
HP:0002017HP:0002013Vomiting1CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional102
HP:0002017HP:0002013Vomiting1CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional1
HP:0002017HP:0002018Nausea1CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional1
HP:0002017HP:0002013Vomiting1CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional
HP:0002017HP:0002018Nausea1CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1CDON CL E G H5093717104ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent200
HP:0002017HP:0002013Vomiting1CDON CL E G H5093717104ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional200
HP:0002017HP:0002013Vomiting1CDON CL E G H5093717104ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent200
HP:0002017HP:0002013Vomiting1CDON CL E G H5093717104ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent200
HP:0002017HP:0002013Vomiting1CFH CL E G H30754883ORPHA:244242HELLP syndromeHP:0040283 - Occasional86
HP:0002017HP:0002018Nausea1CFH CL E G H30754883ORPHA:244242HELLP syndromeHP:0040283 - Occasional86
HP:0002017HP:0002018Nausea1CFI CL E G H34265394ORPHA:244242HELLP syndromeHP:0040283 - Occasional57
HP:0002017HP:0002013Vomiting1CFI CL E G H34265394ORPHA:244242HELLP syndromeHP:0040283 - Occasional57
HP:0002017HP:0002018Nausea1CLCN2 CL E G H11812020ORPHA:404Familial hyperaldosteronism type IIHP:0040283 - Occasional44
HP:0002017HP:0002013Vomiting1CLCNKA CL E G H11872026ORPHA:89938Infantile Bartter syndrome with sensorineural deafnessHP:0040283 - Occasional9
HP:0002017HP:0002013Vomiting1CLCNKB CL E G H11882027ORPHA:89938Infantile Bartter syndrome with sensorineural deafnessHP:0040283 - Occasional27
HP:0002017HP:0002013Vomiting1CLMP CL E G H7982724039OMIM:615237Congenital short bowel syndromeHP:0040283 - Occasional7
HP:0002017HP:0002013Vomiting1COA8 CL E G H8433420492ORPHA:436271Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathyHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1COL1A1 CL E G H12772197ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent373
HP:0002017HP:0002018Nausea1COL1A1 CL E G H12772197ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent373
HP:0002017HP:0002013Vomiting1COL4A5 CL E G H12872207ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent678
HP:0002017HP:0002013Vomiting1COL4A6 CL E G H12882208ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent18
HP:0002017HP:0002018Nausea1COL5A1 CL E G H12892209ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent660
HP:0002017HP:0002013Vomiting1COL5A1 CL E G H12892209ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent660
HP:0002017HP:0002018Nausea1COL5A2 CL E G H12902210ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent325
HP:0002017HP:0002013Vomiting1COL5A2 CL E G H12902210ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent325
HP:0002017HP:0002013Vomiting1COQ2 CL E G H2723525223OMIM:607426Coenzyme Q10 deficiency, primary, 154
HP:0002017HP:0002013Vomiting1COQ2 CL E G H2723525223ORPHA:255249Leigh syndrome with nephrotic syndrome54
HP:0002017HP:0002013Vomiting1COX1 CL E G H45127419ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1COX2 CL E G H45137421ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1COX3 CL E G H45147422ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1CPOX CL E G H13712321OMIM:121300Coproporphyria.72
HP:0002017HP:0002013Vomiting1CPOX CL E G H13712321OMIM:618892Harderoporphyria.72
HP:0002017HP:0002018Nausea1CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyriaHP:0040282 - Frequent72
HP:0002017HP:0002013Vomiting1CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyria72
HP:0002017HP:0002013Vomiting1CPS1 CL E G H13732323OMIM:237300Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to.124
HP:0002017HP:0002013Vomiting1CPT2 CL E G H13762330OMIM:600649Carnitine palmitoyltransferase II deficiency, infantile.101
HP:0002017HP:0002013Vomiting1CPT2 CL E G H13762330OMIM:608836Carnitine palmitoyltransferase II deficiency, lethal neonatal101
HP:0002017HP:0002013Vomiting1CTNNB1 CL E G H14992514ORPHA:33402Pediatric hepatocellular carcinomaHP:0040282 - Frequent88
HP:0002017HP:0002013Vomiting1CTNS CL E G H14972518ORPHA:411629Infantile nephropathic cystinosisHP:0040281 - Very frequent178
HP:0002017HP:0002013Vomiting1CTNS CL E G H14972518ORPHA:411634Juvenile nephropathic cystinosisHP:0040282 - Frequent178
HP:0002017HP:0002013Vomiting1CTRC CL E G H113302523ORPHA:103918Tropical pancreatitis39
HP:0002017HP:0002018Nausea1CTRC CL E G H113302523ORPHA:103918Tropical pancreatitis39
HP:0002017HP:0002013Vomiting1CUBN CL E G H80292548ORPHA:35858Imerslund-Gräsbeck syndromeHP:0040283 - Occasional273
HP:0002017HP:0002013Vomiting1CYC1 CL E G H15372579OMIM:615453Mitochondrial complex III deficiency, nuclear type 612
HP:0002017HP:0002013Vomiting1CYP11A1 CL E G H15832590ORPHA:16855846,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiencyHP:0040281 - Very frequent31
HP:0002017HP:0002013Vomiting1CYP11A1 CL E G H15832590ORPHA:289548Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiencyHP:0040281 - Very frequent31
HP:0002017HP:0002018Nausea1CYP11B1 CL E G H15842591ORPHA:403Familial hyperaldosteronism type IHP:0040283 - Occasional112
HP:0002017HP:0002013Vomiting1CYP11B2 CL E G H15852592OMIM:203400Corticosterone methyloxidase type I deficiency.73
HP:0002017HP:0002013Vomiting1CYP11B2 CL E G H15852592ORPHA:556030Early-onset familial hypoaldosteronismHP:0040282 - Frequent73
HP:0002017HP:0002018Nausea1CYP11B2 CL E G H15852592ORPHA:403Familial hyperaldosteronism type IHP:0040283 - Occasional73
HP:0002017HP:0002013Vomiting1CYP24A1 CL E G H15912602OMIM:143880Hypercalcemia, infantile, 1.73
HP:0002017HP:0002013Vomiting1CYTB CL E G H45197427ORPHA:137675Histiocytoid cardiomyopathyHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1D2HGDH CL E G H72829428358OMIM:600721D-2-Hydroxyglutaric aciduria 1102
HP:0002017HP:0002013Vomiting1DBH CL E G H16212689ORPHA:230Dopamine beta-hydroxylase deficiencyHP:0040283 - Occasional80
HP:0002017HP:0002013Vomiting1DBT CL E G H16292698OMIM:248600Maple syrup urine disease.156
HP:0002017HP:0002013Vomiting1DGAT1 CL E G H86942843OMIM:615863Diarrhea 7, protein-losing Enteropathy type.9
HP:0002017HP:0002013Vomiting1DGUOK CL E G H17162858OMIM:251880Mitochondrial DNA depletion syndrome 3 (hepatocerebral type).57
HP:0002017HP:0002013Vomiting1DHCR7 CL E G H17172860OMIM:270400Smith-Lemli-Opitz syndrome159
HP:0002017HP:0002013Vomiting1DISP1 CL E G H8497619711ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent22
HP:0002017HP:0002013Vomiting1DISP1 CL E G H8497619711ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional22
HP:0002017HP:0002013Vomiting1DISP1 CL E G H8497619711ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent22
HP:0002017HP:0002013Vomiting1DISP1 CL E G H8497619711ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent22
HP:0002017HP:0002013Vomiting1DLD CL E G H17382898ORPHA:2394Pyruvate dehydrogenase E3 deficiencyHP:0040281 - Very frequent89
HP:0002017HP:0002013Vomiting1DLL1 CL E G H285142908ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent3
HP:0002017HP:0002013Vomiting1DLL1 CL E G H285142908ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional3
HP:0002017HP:0002013Vomiting1DLL1 CL E G H285142908ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent3
HP:0002017HP:0002013Vomiting1DLL1 CL E G H285142908ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent3
HP:0002017HP:0002018Nausea1DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent
HP:0002017HP:0002018Nausea1DNAJC6 CL E G H982915469ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional6
HP:0002017HP:0002018Nausea1DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent44
HP:0002017HP:0002013Vomiting1DOLK CL E G H2284523406OMIM:610768Congenital disorder of glycosylation, type Im55
HP:0002017HP:0002013Vomiting1DYRK1A CL E G H18593091ORPHA:464311Intellectual disability syndrome due to a DYRK1A point mutationHP:0040283 - Occasional134
HP:0002017HP:0002013Vomiting1EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 1.3
HP:0002017HP:0002018Nausea1EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 1.3
HP:0002017HP:0002013Vomiting1EGFR CL E G H19563236OMIM:616069Inflammatory skin and bowel disease, neonatal, 2.257
HP:0002017HP:0002013Vomiting1ELN CL E G H20063327ORPHA:90348Autosomal dominant cutis laxa172
HP:0002017HP:0002013Vomiting1ELP1 CL E G H85185959OMIM:223900Neuropathy, hereditary sensory and autonomic, type III.133
HP:0002017HP:0002013Vomiting1ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancyHP:0040283 - Occasional151
HP:0002017HP:0002018Nausea1EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent112
HP:0002017HP:0002013Vomiting1EPCAM CL E G H407211529ORPHA:92050Congenital tufting enteropathyHP:0040284 - Very rare170
HP:0002017HP:0002013Vomiting1ERBB3 CL E G H20653431OMIM:243180Visceral neuropathy, familial, autosomal recessive.12
HP:0002017HP:0002013Vomiting1ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 1.13
HP:0002017HP:0002018Nausea1ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 1.13
HP:0002017HP:0002018Nausea1ETFA CL E G H21083481OMIM:231680Multiple acyl-coa dehydrogenase deficiency.37
HP:0002017HP:0002013Vomiting1ETFA CL E G H21083481OMIM:231680Multiple acyl-coa dehydrogenase deficiency.37
HP:0002017HP:0002018Nausea1ETFB CL E G H21093482OMIM:231680Multiple acyl-coa dehydrogenase deficiency.27
HP:0002017HP:0002013Vomiting1ETFB CL E G H21093482OMIM:231680Multiple acyl-coa dehydrogenase deficiency.27
HP:0002017HP:0002018Nausea1ETFDH CL E G H21103483OMIM:231680Multiple acyl-coa dehydrogenase deficiency.77
HP:0002017HP:0002013Vomiting1ETFDH CL E G H21103483OMIM:231680Multiple acyl-coa dehydrogenase deficiency.77
HP:0002017HP:0002018Nausea1EXT2 CL E G H21323513ORPHA:466926Seizures-scoliosis-macrocephaly syndromeHP:0040282 - Frequent102
HP:0002017HP:0002013Vomiting1F12 CL E G H21613530OMIM:610618ANGIOEDEMA, HEREDITARY, TYPE III; HAE328
HP:0002017HP:0002013Vomiting1FAH CL E G H21843579OMIM:276700Tyrosinemia, type I107
HP:0002017HP:0002013Vomiting1FARSB CL E G H1005617800OMIM:613658Rajab interstitial lung disease with brain calcifications
HP:0002017HP:0002013Vomiting1FBLN5 CL E G H105163602ORPHA:90348Autosomal dominant cutis laxa63
HP:0002017HP:0002013Vomiting1FBP1 CL E G H22033606ORPHA:348Fructose-1,6-bisphosphatase deficiencyHP:0040282 - Frequent64
HP:0002017HP:0002013Vomiting1FGF8 CL E G H22533686ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent17
HP:0002017HP:0002013Vomiting1FGF8 CL E G H22533686ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional17
HP:0002017HP:0002013Vomiting1FGF8 CL E G H22533686ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent17
HP:0002017HP:0002013Vomiting1FGF8 CL E G H22533686ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent17
HP:0002017HP:0002013Vomiting1FGFR1 CL E G H22603688ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional172
HP:0002017HP:0002013Vomiting1FGFR1 CL E G H22603688ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent172
HP:0002017HP:0002018Nausea1FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent301
HP:0002017HP:0002013Vomiting1FLNA CL E G H23163754OMIM:300048Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked.493
HP:0002017HP:0002013Vomiting1FOCAD CL E G H5491423377OMIM:6199913
HP:0002017HP:0002013Vomiting1FOXH1 CL E G H89283814ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent48
HP:0002017HP:0002013Vomiting1FOXH1 CL E G H89283814ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional48
HP:0002017HP:0002013Vomiting1FOXH1 CL E G H89283814ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent48
HP:0002017HP:0002013Vomiting1FOXH1 CL E G H89283814ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent48
HP:0002017HP:0002013Vomiting1FOXP3 CL E G H509436106ORPHA:37042Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndromeHP:0040283 - Occasional32
HP:0002017HP:0002013Vomiting1FOXRED1 CL E G H5557226927ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent61
HP:0002017HP:0002018Nausea1FSHR CL E G H24923969OMIM:608115Ovarian hyperstimulation syndrome.50
HP:0002017HP:0002018Nausea1FSHR CL E G H24923969ORPHA:64739Ovarian hyperstimulation syndromeHP:0040281 - Very frequent50
HP:0002017HP:0002013Vomiting1GALC CL E G H25814115ORPHA:206436Infantile Krabbe diseaseHP:0040283 - Occasional160
HP:0002017HP:0002013Vomiting1GALC CL E G H25814115OMIM:245200Krabbe disease.160
HP:0002017HP:0002013Vomiting1GALE CL E G H25824116OMIM:230350Galactose epimerase deficiency.52
HP:0002017HP:0002013Vomiting1GALT CL E G H25924135ORPHA:79239Classic galactosemiaHP:0040282 - Frequent351
HP:0002017HP:0002013Vomiting1GALT CL E G H25924135OMIM:230400GALACTOSEMIA.351
HP:0002017HP:0002013Vomiting1GAMT CL E G H25934136OMIM:612736Cerebral creatine deficiency syndrome 291
HP:0002017HP:0002013Vomiting1GAN CL E G H81394137OMIM:256850Giant axonal neuropathy 1, autosomal recessive121
HP:0002017HP:0002013Vomiting1GAS1 CL E G H26194165ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent2
HP:0002017HP:0002013Vomiting1GAS1 CL E G H26194165ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional2
HP:0002017HP:0002013Vomiting1GAS1 CL E G H26194165ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent2
HP:0002017HP:0002013Vomiting1GAS1 CL E G H26194165ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent2
HP:0002017HP:0002013Vomiting1GFAP CL E G H26704235ORPHA:363717Alexander disease type I188
HP:0002017HP:0002013Vomiting1GFM2 CL E G H8434029682ORPHA:565624Combined oxidative phosphorylation defect type 39HP:0040283 - Occasional43
HP:0002017HP:0002013Vomiting1GHSR CL E G H26934267ORPHA:314811Short stature due to GHSR deficiencyHP:0040281 - Very frequent37
HP:0002017HP:0002013Vomiting1GK CL E G H27104289OMIM:307030Glycerol kinase deficiency13
HP:0002017HP:0002013Vomiting1GLA CL E G H27174296OMIM:301500Fabry disease.291
HP:0002017HP:0002018Nausea1GLA CL E G H27174296OMIM:301500Fabry disease.291
HP:0002017HP:0002013Vomiting1GLI2 CL E G H27364318ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent173
HP:0002017HP:0002013Vomiting1GLI2 CL E G H27364318ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional173
HP:0002017HP:0002013Vomiting1GLI2 CL E G H27364318ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent173
HP:0002017HP:0002013Vomiting1GLI2 CL E G H27364318ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent173
HP:0002017HP:0002013Vomiting1GRB10 CL E G H28874564ORPHA:96182Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7HP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1HADH CL E G H30334799ORPHA:71212Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiencyHP:0040281 - Very frequent41
HP:0002017HP:0002013Vomiting1HELLPAR CL E G H10110169243984ORPHA:244242HELLP syndromeHP:0040283 - Occasional
HP:0002017HP:0002018Nausea1HELLPAR CL E G H10110169243984ORPHA:244242HELLP syndromeHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1HFE CL E G H30774886OMIM:176200Porphyria variegata.38
HP:0002017HP:0002013Vomiting1HIBCH CL E G H262754908ORPHA:88639Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiencyHP:0040281 - Very frequent32
HP:0002017HP:0002013Vomiting1HLA-DQA1 CL E G H31174942OMIM:212750Celiac disease, susceptibility to, 1.
HP:0002017HP:0002013Vomiting1HLA-DQB1 CL E G H31194944OMIM:212750Celiac disease, susceptibility to, 1.
HP:0002017HP:0002013Vomiting1HLCS CL E G H31414976OMIM:253270Holocarboxylase synthetase deficiency.148
HP:0002017HP:0002018Nausea1HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent.81
HP:0002017HP:0002013Vomiting1HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent.81
HP:0002017HP:0002013Vomiting1HMGCL CL E G H31555005ORPHA:203-hydroxy-3-methylglutaric aciduria35
HP:0002017HP:0002013Vomiting1HMGCL CL E G H31555005OMIM:2464503-Hydroxy-3-Methylglutaryl-Coa lyase deficiency.35
HP:0002017HP:0002013Vomiting1HMGCS2 CL E G H31585008OMIM:6059113-Hydroxy-3-Methylglutaryl-Coa synthase-2 deficiency.42
HP:0002017HP:0002013Vomiting1HNF4A CL E G H31725024ORPHA:263455Hyperinsulinism due to HNF4A deficiencyHP:0040282 - Frequent138
HP:0002017HP:0002013Vomiting1HNRNPK CL E G H31905044ORPHA:352665Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion8
HP:0002017HP:0002013Vomiting1HNRNPK CL E G H31905044ORPHA:453504Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation8
HP:0002017HP:0002013Vomiting1HPRT1 CL E G H32515157OMIM:300322Lesch-Nyhan syndrome.76
HP:0002017HP:0002013Vomiting1HS3ST6 CL E G H6471114178OMIM:619367ANGIOEDEMA, HEREDITARY, 8; HAE8
HP:0002017HP:0002013Vomiting1HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiencyHP:0040282 - Frequent34
HP:0002017HP:0002018Nausea1HTRA2 CL E G H2742914348ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional39
HP:0002017HP:0002018Nausea1IL18BP CL E G H100685987OMIM:618549HEPATITIS, FULMINANT VIRAL, SUSCEPTIBILITY TO; FVH
HP:0002017HP:0002013Vomiting1IRAK1 CL E G H36546112ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1ITGB4 CL E G H36916158ORPHA:158684Epidermolysis bullosa simplex with pyloric atresiaHP:0040282 - Frequent124
HP:0002017HP:0002013Vomiting1IVD CL E G H37126186OMIM:243500Isovaleric acidemia.105
HP:0002017HP:0002013Vomiting1KARS1 CL E G H37356215OMIM:619147LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS; LEPID
HP:0002017HP:0002018Nausea1KCNA1 CL E G H37366218ORPHA:37612Episodic ataxia type 1HP:0040282 - Frequent145
HP:0002017HP:0002013Vomiting1KCNJ1 CL E G H37586255OMIM:241200Bartter syndrome, antenatal, type 2.51
HP:0002017HP:0002013Vomiting1KCNJ11 CL E G H37676257ORPHA:79134DEND syndromeHP:0040283 - Occasional127
HP:0002017HP:0002018Nausea1KCNJ5 CL E G H37626266ORPHA:251274Familial hyperaldosteronism type IIIHP:0040283 - Occasional128
HP:0002017HP:0002018Nausea1KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent202
HP:0002017HP:0002018Nausea1KIT CL E G H38156342ORPHA:79455Cutaneous mastocytoma327
HP:0002017HP:0002013Vomiting1KIT CL E G H38156342ORPHA:79455Cutaneous mastocytoma327
HP:0002017HP:0002018Nausea1KIT CL E G H38156342ORPHA:98849Systemic mastocytosis with associated hematologic neoplasmHP:0040283 - Occasional327
HP:0002017HP:0002013Vomiting1KMT2E CL E G H5590418541OMIM:618512O'donnell-Luria-Rodan syndrome.1
HP:0002017HP:0002013Vomiting1KRIT1 CL E G H8891573ORPHA:221061Familial cerebral cavernous malformation92
HP:0002017HP:0002013Vomiting1KYNU CL E G H89426469OMIM:236800HYDROXYKYNURENINURIA5
HP:0002017HP:0002013Vomiting1LAMA3 CL E G H39096483ORPHA:79404Severe generalized junctional epidermolysis bullosaHP:0040283 - Occasional116
HP:0002017HP:0002013Vomiting1LAMB3 CL E G H39146490ORPHA:79404Severe generalized junctional epidermolysis bullosaHP:0040283 - Occasional167
HP:0002017HP:0002013Vomiting1LAMC2 CL E G H39186493ORPHA:79404Severe generalized junctional epidermolysis bullosaHP:0040283 - Occasional135
HP:0002017HP:0002013Vomiting1LBX1 CL E G H1066016960OMIM:619483CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3; CCHS3
HP:0002017HP:0002018Nausea1LIG3 CL E G H39806600ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent1
HP:0002017HP:0002013Vomiting1LIG3 CL E G H39806600ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent1
HP:0002017HP:0002013Vomiting1LIPA CL E G H39886617OMIM:278000Lysosomal acid lipase deficiency73
HP:0002017HP:0002018Nausea1LPL CL E G H40236677OMIM:238600Type I hyperlipoproteinemia.106
HP:0002017HP:0002013Vomiting1LPL CL E G H40236677OMIM:238600Type I hyperlipoproteinemia.106
HP:0002017HP:0002018Nausea1LRRK2 CL E G H12089218618ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional221
HP:0002017HP:0002013Vomiting1MARS1 CL E G H41416898OMIM:615486Interstitial lung and liver disease
HP:0002017HP:0002018Nausea1MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent84
HP:0002017HP:0002013Vomiting1MC2R CL E G H41586930ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent94
HP:0002017HP:0002013Vomiting1MCCC1 CL E G H569226936OMIM:2102003-Methylcrotonyl-CoA carboxylase 1 deficiency.81
HP:0002017HP:0002013Vomiting1MCCC2 CL E G H640876937OMIM:2102103-Methylcrotonyl-CoA carboxylase 2 deficiency.77
HP:0002017HP:0002018Nausea1MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent4
HP:0002017HP:0002013Vomiting1MED12 CL E G H996811957OMIM:301068HARDIKAR SYNDROME; HDKR228
HP:0002017HP:0002013Vomiting1MEFV CL E G H42106998OMIM:249100Familial Mediterranean fever, AR281
HP:0002017HP:0002018Nausea1MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional462
HP:0002017HP:0002013Vomiting1MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional462
HP:0002017HP:0002013Vomiting1MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040282 - Frequent462
HP:0002017HP:0002013Vomiting1MET CL E G H42337029ORPHA:33402Pediatric hepatocellular carcinomaHP:0040282 - Frequent375
HP:0002017HP:0002018Nausea1MGME1 CL E G H9266716205OMIM:615084Mitochondrial DNA depletion syndrome 11HP:0040283 - Occasional11
HP:0002017HP:0002018Nausea1MGME1 CL E G H9266716205ORPHA:352447Progressive external ophthalmoplegia-myopathy-emaciation syndromeHP:0040282 - Frequent11
HP:0002017HP:0002013Vomiting1MLYCD CL E G H234177150OMIM:248360Malonyl-CoA decarboxylase deficiency.80
HP:0002017HP:0002013Vomiting1MMAA CL E G H16678518871OMIM:251100Methylmalonic aciduria, Cbla type.113
HP:0002017HP:0002013Vomiting1MMAB CL E G H32662519331OMIM:251110Methylmalonic aciduria, Cblb type.127
HP:0002017HP:0002013Vomiting1MMUT CL E G H45947526OMIM:251000Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency.
HP:0002017HP:0002013Vomiting1MPI CL E G H43517216OMIM:602579Congenital disorder of glycosylation, type Ib.51
HP:0002017HP:0002013Vomiting1MPI CL E G H43517216ORPHA:79319MPI-CDGHP:0040282 - Frequent51
HP:0002017HP:0002013Vomiting1MPV17 CL E G H43587224OMIM:256810Navajo neurohepatopathy.56
HP:0002017HP:0002013Vomiting1MRAP CL E G H562461304ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent26
HP:0002017HP:0002013Vomiting1MRPS7 CL E G H5108114499OMIM:617872Combined oxidative phosphorylation deficiency 34.12
HP:0002017HP:0002013Vomiting1MSX2 CL E G H44887392ORPHA:60015Enlarged parietal foraminaHP:0040283 - Occasional45
HP:0002017HP:0002013Vomiting1MTHFD1 CL E G H45227432OMIM:617780Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia.5
HP:0002017HP:0002013Vomiting1MTRR CL E G H45527473ORPHA:2169Methylcobalamin deficiency type cblEHP:0040282 - Frequent88
HP:0002017HP:0002013Vomiting1MTTP CL E G H45477467ORPHA:14AbetalipoproteinemiaHP:0040283 - Occasional81
HP:0002017HP:0002013Vomiting1MVK CL E G H45987530OMIM:260920Hyper-Igd syndrome150
HP:0002017HP:0002013Vomiting1MVK CL E G H45987530OMIM:610377Mevalonic aciduria150
HP:0002017HP:0002013Vomiting1NAA10 CL E G H826018704OMIM:300855Ogden syndrome23
HP:0002017HP:0002013Vomiting1NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiencyHP:0040282 - Frequent36
HP:0002017HP:0002018Nausea1NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiencyHP:0040282 - Frequent36
HP:0002017HP:0002013Vomiting1NAGS CL E G H16241717996OMIM:237310N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY.36
HP:0002017HP:0002013Vomiting1NARS2 CL E G H7973126274ORPHA:79134DEND syndromeHP:0040283 - Occasional34
HP:0002017HP:0002013Vomiting1NAXD CL E G H5573925576OMIM:618321Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2.
HP:0002017HP:0002013Vomiting1NBAS CL E G H5159415625OMIM:616483INFANTILE LIVER FAILURE SYNDROME 2; ILFS225
HP:0002017HP:0002013Vomiting1ND1 CL E G H45357455ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002017HP:0002013Vomiting1ND1 CL E G H45357455ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1ND1 CL E G H45357455ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1ND2 CL E G H45367456ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002017HP:0002013Vomiting1ND2 CL E G H45367456ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ND3 CL E G H45377458ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002017HP:0002013Vomiting1ND3 CL E G H45377458ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ND4 CL E G H45387459ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1ND4 CL E G H45387459ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ND5 CL E G H45407461ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1ND5 CL E G H45407461ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1ND6 CL E G H45417462ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1ND6 CL E G H45417462ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1NDUFA1 CL E G H46947683ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent7
HP:0002017HP:0002013Vomiting1NDUFA11 CL E G H12632820371ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent32
HP:0002017HP:0002013Vomiting1NDUFA6 CL E G H47007690ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent1
HP:0002017HP:0002013Vomiting1NDUFAF1 CL E G H5110318828ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent40
HP:0002017HP:0002013Vomiting1NDUFAF2 CL E G H9194228086ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent26
HP:0002017HP:0002013Vomiting1NDUFAF3 CL E G H2591529918ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent31
HP:0002017HP:0002013Vomiting1NDUFAF4 CL E G H2907821034ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent50
HP:0002017HP:0002013Vomiting1NDUFAF5 CL E G H7913315899ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent34
HP:0002017HP:0002013Vomiting1NDUFAF8 CL E G H28418433551ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002017HP:0002013Vomiting1NDUFB10 CL E G H47167696ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002017HP:0002013Vomiting1NDUFB11 CL E G H5453920372ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent3
HP:0002017HP:0002013Vomiting1NDUFB3 CL E G H47097698ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent9
HP:0002017HP:0002013Vomiting1NDUFB9 CL E G H47157704ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent16
HP:0002017HP:0002013Vomiting1NDUFS1 CL E G H47197707ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent81
HP:0002017HP:0002013Vomiting1NDUFS1 CL E G H47197707OMIM:618226Mitochondrial complex I deficiency, nuclear type 5.81
HP:0002017HP:0002013Vomiting1NDUFS2 CL E G H47207708ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent65
HP:0002017HP:0002013Vomiting1NDUFS3 CL E G H47227710ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent22
HP:0002017HP:0002013Vomiting1NDUFS4 CL E G H47247711ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent27
HP:0002017HP:0002013Vomiting1NDUFS4 CL E G H47247711OMIM:252010Mitochondrial complex I deficiency, nuclear type 127
HP:0002017HP:0002013Vomiting1NDUFS6 CL E G H47267713ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent21
HP:0002017HP:0002013Vomiting1NDUFS7 CL E G H3742917714ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent38
HP:0002017HP:0002013Vomiting1NDUFS8 CL E G H47287715ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent42
HP:0002017HP:0002013Vomiting1NDUFV1 CL E G H47237716ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent74
HP:0002017HP:0002013Vomiting1NDUFV1 CL E G H47237716OMIM:618225Mitochondrial complex I deficiency, nuclear type 4.74
HP:0002017HP:0002013Vomiting1NDUFV2 CL E G H47297717ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent27
HP:0002017HP:0002013Vomiting1NEUROG3 CL E G H5067413806OMIM:610370Diarrhea 4, malabsorptive, congenital.5
HP:0002017HP:0002013Vomiting1NEUROG3 CL E G H5067413806ORPHA:83620Enteric anendocrinosisHP:0040281 - Very frequent5
HP:0002017HP:0002013Vomiting1NEXMIF CL E G H34053329433OMIM:300912Mental retardation, X-linked 9852
HP:0002017HP:0002018Nausea1NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent1952
HP:0002017HP:0002013Vomiting1NFIX CL E G H47847788ORPHA:44798019p13.3 microduplication syndrome40
HP:0002017HP:0002013Vomiting1NLRC4 CL E G H5848416412OMIM:616050AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC30
HP:0002017HP:0002013Vomiting1NNT CL E G H235307863ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent13
HP:0002017HP:0002013Vomiting1NODAL CL E G H48387865ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent45
HP:0002017HP:0002013Vomiting1NODAL CL E G H48387865ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional45
HP:0002017HP:0002013Vomiting1NODAL CL E G H48387865ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent45
HP:0002017HP:0002013Vomiting1NODAL CL E G H48387865ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent45
HP:0002017HP:0002013Vomiting1NOTCH2NLC CL E G H10099671753924OMIM:603472NEURONAL INTRANUCLEAR INCLUSION DISEASE
HP:0002017HP:0002018Nausea1NPPA CL E G H48787939ORPHA:1344Atrial standstillHP:0040283 - Occasional13
HP:0002017HP:0002013Vomiting1NR3C2 CL E G H43067979OMIM:177735Pseudohypoaldosteronism, type I, autosomal dominant.109
HP:0002017HP:0002013Vomiting1NSD1 CL E G H6432414234OMIM:117550Sotos syndrome 1544
HP:0002017HP:0002013Vomiting1NUBPL CL E G H8022420278ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent89
HP:0002017HP:0002013Vomiting1OPLAH CL E G H268738149OMIM:2600055-@oxoprolinase deficiency.5
HP:0002017HP:0002013Vomiting1OTC CL E G H50098512OMIM:311250Ornithine transcarbamylase deficiency, hyperammonemia due to.369
HP:0002017HP:0002013Vomiting1OXCT1 CL E G H50198527OMIM:245050Succinyl CoA:3-oxoacid CoA transferase deficiency.52
HP:0002017HP:0002018Nausea1PARK7 CL E G H1131516369ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional23
HP:0002017HP:0002013Vomiting1PCCA CL E G H50958653OMIM:606054Propionic acidemia.96
HP:0002017HP:0002013Vomiting1PCCB CL E G H50968654OMIM:606054Propionic acidemia.92
HP:0002017HP:0002013Vomiting1PDCD10 CL E G H112358761ORPHA:221061Familial cerebral cavernous malformation21
HP:0002017HP:0002013Vomiting1PDSS2 CL E G H5710723041ORPHA:255249Leigh syndrome with nephrotic syndrome54
HP:0002017HP:0002013Vomiting1PERCC1 CL E G H10537104552293ORPHA:92050Congenital tufting enteropathyHP:0040284 - Very rare
HP:0002017HP:0002013Vomiting1PGM1 CL E G H52368905OMIM:614921Congenital disorder of glycosylation, type It58
HP:0002017HP:0002013Vomiting1PHGDH CL E G H262278923ORPHA:793513-phosphoglycerate dehydrogenase deficiency, infantile/juvenile formHP:0040282 - Frequent37
HP:0002017HP:0002018Nausea1PHKA2 CL E G H52568926ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiencyHP:0040284 - Very rare54
HP:0002017HP:0002013Vomiting1PHKA2 CL E G H52568926ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiencyHP:0040284 - Very rare54
HP:0002017HP:0002013Vomiting1PHKB CL E G H52578927ORPHA:79240Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency101
HP:0002017HP:0002018Nausea1PHKB CL E G H52578927ORPHA:79240Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency101
HP:0002017HP:0002013Vomiting1PHKG2 CL E G H52618931ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiencyHP:0040284 - Very rare48
HP:0002017HP:0002018Nausea1PHKG2 CL E G H52618931ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiencyHP:0040284 - Very rare48
HP:0002017HP:0002013Vomiting1PIGY CL E G H8499228213OMIM:616809Hyperphosphatasia with mental retardation syndrome 62
HP:0002017HP:0002018Nausea1PINK1 CL E G H6501814581ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional55
HP:0002017HP:0002013Vomiting1PKHD1 CL E G H53149016ORPHA:53035Caroli diseaseHP:0040283 - Occasional563
HP:0002017HP:0002018Nausea1PKHD1 CL E G H53149016ORPHA:53035Caroli diseaseHP:0040283 - Occasional563
HP:0002017HP:0002013Vomiting1PLCH1 CL E G H2300729185ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1PLEC CL E G H53399069ORPHA:158684Epidermolysis bullosa simplex with pyloric atresiaHP:0040282 - Frequent759
HP:0002017HP:0002013Vomiting1PMM2 CL E G H53739115OMIM:212065Congenital disorder of glycosylation, type Ia.150
HP:0002017HP:0002013Vomiting1PMM2 CL E G H53739115ORPHA:79318PMM2-CDGHP:0040282 - Frequent150
HP:0002017HP:0002013Vomiting1PNPLA8 CL E G H5064028900OMIM:251950Mitochondrial myopathy with lactic acidosis3
HP:0002017HP:0002013Vomiting1PNPT1 CL E G H8717823166OMIM:608703Spinocerebellar ataxia 25.60
HP:0002017HP:0002013Vomiting1PNPT1 CL E G H8717823166ORPHA:101111Spinocerebellar ataxia type 25HP:0040283 - Occasional60
HP:0002017HP:0002018Nausea1PODXL CL E G H54209171ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional6
HP:0002017HP:0002013Vomiting1POLG CL E G H54289179OMIM:603041Mitochondrial DNA depletion syndrome 1 (mngie type).464
HP:0002017HP:0002013Vomiting1POLG CL E G H54289179OMIM:203700Mitochondrial DNA depletion syndrome 4A (Alpers type).464
HP:0002017HP:0002018Nausea1POLG CL E G H54289179ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent464
HP:0002017HP:0002013Vomiting1POLG CL E G H54289179ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent464
HP:0002017HP:0002013Vomiting1PPM1D CL E G H84939277OMIM:617450Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold.22
HP:0002017HP:0002013Vomiting1PPOX CL E G H54989280OMIM:176200Porphyria variegata.41
HP:0002017HP:0002018Nausea1PPOX CL E G H54989280ORPHA:79473Porphyria variegataHP:0040283 - Occasional41
HP:0002017HP:0002018Nausea1PRKN CL E G H50718607ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional138
HP:0002017HP:0002013Vomiting1PSAP CL E G H56609498ORPHA:206436Infantile Krabbe diseaseHP:0040283 - Occasional81
HP:0002017HP:0002013Vomiting1PTCH1 CL E G H57279585ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent665
HP:0002017HP:0002013Vomiting1PTCH1 CL E G H57279585ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional665
HP:0002017HP:0002013Vomiting1PTCH1 CL E G H57279585ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent665
HP:0002017HP:0002013Vomiting1PTCH1 CL E G H57279585ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent665
HP:0002017HP:0002013Vomiting1PYCR2 CL E G H2992030262ORPHA:481152PYCR2-related microcephaly-progressive leukoencephalopathyHP:0040282 - Frequent11
HP:0002017HP:0002013Vomiting1RANBP2 CL E G H59039848ORPHA:88619Familial acute necrotizing encephalopathyHP:0040282 - Frequent57
HP:0002017HP:0002013Vomiting1RARS1 CL E G H59179870ORPHA:438114RARS-related autosomal recessive hypomyelinating leukodystrophyHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1RECQL4 CL E G H94019949ORPHA:221016Rothmund-Thomson syndrome type 2HP:0040283 - Occasional445
HP:0002017HP:0002013Vomiting1RELA CL E G H59709955ORPHA:251636EpendymomaHP:0040283 - Occasional1
HP:0002017HP:0002018Nausea1RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent572
HP:0002017HP:0002013Vomiting1RET CL E G H59799967OMIM:142623Hirschsprung disease, susceptibility to, 1.572
HP:0002017HP:0002018Nausea1RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent572
HP:0002017HP:0002013Vomiting1RRM2B CL E G H5048417296OMIM:612075Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)125
HP:0002017HP:0002013Vomiting1RRM2B CL E G H5048417296ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent125
HP:0002017HP:0002018Nausea1RRM2B CL E G H5048417296ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent125
HP:0002017HP:0002013Vomiting1RYR1 CL E G H626110483ORPHA:466650Exercise-induced malignant hyperthermiaHP:0040283 - Occasional1200
HP:0002017HP:0002018Nausea1RYR1 CL E G H626110483ORPHA:466650Exercise-induced malignant hyperthermiaHP:0040282 - Frequent1200
HP:0002017HP:0002018Nausea1SAA1 CL E G H628810513ORPHA:85445AA amyloidosisHP:0040282 - Frequent2
HP:0002017HP:0002013Vomiting1SAA1 CL E G H628810513ORPHA:85445AA amyloidosisHP:0040282 - Frequent2
HP:0002017HP:0002013Vomiting1SAR1B CL E G H5112810535ORPHA:71Chylomicron retention diseaseHP:0040282 - Frequent8
HP:0002017HP:0002013Vomiting1SAR1B CL E G H5112810535OMIM:246700Chylomicron retention disease.8
HP:0002017HP:0002013Vomiting1SCN2A CL E G H632610588OMIM:618924EPISODIC ATAXIA, TYPE 9; EA9427
HP:0002017HP:0002018Nausea1SCN5A CL E G H633110593ORPHA:1344Atrial standstillHP:0040283 - Occasional1134
HP:0002017HP:0002013Vomiting1SCNN1A CL E G H633710599ORPHA:171876Generalized pseudohypoaldosteronism type 1HP:0040282 - Frequent67
HP:0002017HP:0002013Vomiting1SCNN1A CL E G H633710599OMIM:264350Pseudohypoaldosteronism, type I, autosomal recessive.67
HP:0002017HP:0002013Vomiting1SCNN1B CL E G H633810600ORPHA:171876Generalized pseudohypoaldosteronism type 1HP:0040282 - Frequent61
HP:0002017HP:0002013Vomiting1SCNN1G CL E G H634010602ORPHA:171876Generalized pseudohypoaldosteronism type 1HP:0040282 - Frequent57
HP:0002017HP:0002018Nausea1SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent304
HP:0002017HP:0002018Nausea1SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent55
HP:0002017HP:0002018Nausea1SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent237
HP:0002017HP:0002018Nausea1SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent237
HP:0002017HP:0002018Nausea1SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent147
HP:0002017HP:0002018Nausea1SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent129
HP:0002017HP:0002018Nausea1SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent129
HP:0002017HP:0002013Vomiting1SERPING1 CL E G H7101228OMIM:106100Angioedema, hereditary, 1.64
HP:0002017HP:0002013Vomiting1SERPING1 CL E G H7101228ORPHA:100050Hereditary angioedema type 1HP:0040282 - Frequent64
HP:0002017HP:0002018Nausea1SERPING1 CL E G H7101228ORPHA:100050Hereditary angioedema type 1HP:0040282 - Frequent64
HP:0002017HP:0002013Vomiting1SHANK3 CL E G H8535814294OMIM:606232Phelan-Mcdermid syndrome53
HP:0002017HP:0002013Vomiting1SHH CL E G H646910848ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent67
HP:0002017HP:0002013Vomiting1SHH CL E G H646910848ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional67
HP:0002017HP:0002013Vomiting1SHH CL E G H646910848ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent67
HP:0002017HP:0002013Vomiting1SHH CL E G H646910848ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent67
HP:0002017HP:0002013Vomiting1SI CL E G H647610856ORPHA:35122Congenital sucrase-isomaltase deficiencyHP:0040282 - Frequent98
HP:0002017HP:0002013Vomiting1SIX3 CL E G H649610889ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent32
HP:0002017HP:0002013Vomiting1SIX3 CL E G H649610889ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional32
HP:0002017HP:0002013Vomiting1SIX3 CL E G H649610889ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent32
HP:0002017HP:0002013Vomiting1SIX3 CL E G H649610889ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent32
HP:0002017HP:0002013Vomiting1SLC12A1 CL E G H655710910OMIM:601678Bartter syndrome, type 1, antenatal.75
HP:0002017HP:0002013Vomiting1SLC12A3 CL E G H655910912OMIM:263800Gitelman syndrome145
HP:0002017HP:0002013Vomiting1SLC19A3 CL E G H8070416266OMIM:607483Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)110
HP:0002017HP:0002013Vomiting1SLC1A3 CL E G H650710941ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent63
HP:0002017HP:0002018Nausea1SLC1A3 CL E G H650710941OMIM:612656Episodic ataxia, type 6.63
HP:0002017HP:0002013Vomiting1SLC1A3 CL E G H650710941OMIM:612656Episodic ataxia, type 6.63
HP:0002017HP:0002018Nausea1SLC22A12 CL E G H11608517989ORPHA:94088Hereditary renal hypouricemiaHP:0040283 - Occasional56
HP:0002017HP:0002013Vomiting1SLC22A12 CL E G H11608517989ORPHA:94088Hereditary renal hypouricemiaHP:0040283 - Occasional56
HP:0002017HP:0002013Vomiting1SLC22A5 CL E G H658410969OMIM:212140Carnitine deficiency, systemic primary.207
HP:0002017HP:0002013Vomiting1SLC22A5 CL E G H658410969ORPHA:158Systemic primary carnitine deficiencyHP:0040281 - Very frequent207
HP:0002017HP:0002018Nausea1SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040283 - Occasional82
HP:0002017HP:0002013Vomiting1SLC25A15 CL E G H1016610985OMIM:238970Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome88
HP:0002017HP:0002013Vomiting1SLC25A15 CL E G H1016610985ORPHA:415Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome88
HP:0002017HP:0002018Nausea1SLC2A9 CL E G H5660613446ORPHA:94088Hereditary renal hypouricemiaHP:0040283 - Occasional57
HP:0002017HP:0002013Vomiting1SLC2A9 CL E G H5660613446ORPHA:94088Hereditary renal hypouricemiaHP:0040283 - Occasional57
HP:0002017HP:0002013Vomiting1SLC37A4 CL E G H25424061OMIM:619525CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw; CDG2W110
HP:0002017HP:0002013Vomiting1SLC5A1 CL E G H652311036ORPHA:35710Glucose-galactose malabsorptionHP:0040283 - Occasional74
HP:0002017HP:0002013Vomiting1SLC5A6 CL E G H888411041OMIM:618973NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE; NERIB
HP:0002017HP:0002013Vomiting1SLC6A8 CL E G H653511055OMIM:300352Creatine deficiency syndrome, X-linked.122
HP:0002017HP:0002018Nausea1SLC7A7 CL E G H905611065OMIM:222700Lysinuric protein intolerance.104
HP:0002017HP:0002013Vomiting1SLC7A7 CL E G H905611065OMIM:222700Lysinuric protein intolerance.104
HP:0002017HP:0002013Vomiting1SLC7A7 CL E G H905611065ORPHA:470Lysinuric protein intoleranceHP:0040282 - Frequent104
HP:0002017HP:0002013Vomiting1SMC1A CL E G H824311111ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent135
HP:0002017HP:0002013Vomiting1SMPD1 CL E G H660911120OMIM:257200Niemann-Pick disease, type A.164
HP:0002017HP:0002018Nausea1SNCA CL E G H662211138ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional65
HP:0002017HP:0002018Nausea1SPINK1 CL E G H669011244ORPHA:103918Tropical pancreatitis34
HP:0002017HP:0002013Vomiting1SPINK1 CL E G H669011244ORPHA:103918Tropical pancreatitis34
HP:0002017HP:0002013Vomiting1SPP1 CL E G H669611255ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1SPTBN1 CL E G H671111275OMIM:619475DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA
HP:0002017HP:0002018Nausea1SRSF2 CL E G H642710783ORPHA:98849Systemic mastocytosis with associated hematologic neoplasmHP:0040283 - Occasional1
HP:0002017HP:0002013Vomiting1SSR4 CL E G H674811326ORPHA:370927SSR4-CDGHP:0040281 - Very frequent12
HP:0002017HP:0002013Vomiting1ST3GAL5 CL E G H886910872OMIM:609056Salt and pepper developmental regression syndrome.47
HP:0002017HP:0002013Vomiting1STAG2 CL E G H1073511355ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent1
HP:0002017HP:0002013Vomiting1STAG2 CL E G H1073511355ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent1
HP:0002017HP:0002013Vomiting1STAR CL E G H677011359ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent45
HP:0002017HP:0002013Vomiting1STAT4 CL E G H677511365ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional2
HP:0002017HP:0002013Vomiting1STIL CL E G H649110879ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent99
HP:0002017HP:0002013Vomiting1STIL CL E G H649110879ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional99
HP:0002017HP:0002013Vomiting1STIL CL E G H649110879ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent99
HP:0002017HP:0002013Vomiting1STIL CL E G H649110879ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent99
HP:0002017HP:0002013Vomiting1STK11 CL E G H679411389ORPHA:2869Peutz-Jeghers syndromeHP:0040283 - Occasional740
HP:0002017HP:0002013Vomiting1STX3 CL E G H680911438OMIM:619445DIARRHEA 12, WITH MICROVILLUS ATROPHY; DIAR121
HP:0002017HP:0002013Vomiting1SUCLG1 CL E G H880211449ORPHA:17Fatal infantile lactic acidosis with methylmalonic aciduriaHP:0040283 - Occasional60
HP:0002017HP:0002013Vomiting1SUGCT CL E G H7978316001OMIM:231690Glutaric aciduria III.8
HP:0002017HP:0002013Vomiting1SUOX CL E G H682111460OMIM:272300SULFOCYSTEINURIA40
HP:0002017HP:0002013Vomiting1SYK CL E G H685011491OMIM:619381IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION; IMD821
HP:0002017HP:0002018Nausea1SYNJ1 CL E G H886711503ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional9
HP:0002017HP:0002013Vomiting1SYT1 CL E G H685711509ORPHA:522077Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndromeHP:0040282 - Frequent1
HP:0002017HP:0002013Vomiting1TCN2 CL E G H694811653OMIM:275350Transcobalamin II deficiency.57
HP:0002017HP:0002013Vomiting1TDGF1 CL E G H699711701ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent1
HP:0002017HP:0002013Vomiting1TDGF1 CL E G H699711701ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional1
HP:0002017HP:0002013Vomiting1TDGF1 CL E G H699711701ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent1
HP:0002017HP:0002013Vomiting1TDGF1 CL E G H699711701ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent1
HP:0002017HP:0002018Nausea1TET2 CL E G H5479025941ORPHA:98849Systemic mastocytosis with associated hematologic neoplasmHP:0040283 - Occasional3
HP:0002017HP:0002013Vomiting1TGIF1 CL E G H705011776ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent32
HP:0002017HP:0002013Vomiting1TGIF1 CL E G H705011776ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional32
HP:0002017HP:0002013Vomiting1TGIF1 CL E G H705011776ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent32
HP:0002017HP:0002013Vomiting1TGIF1 CL E G H705011776ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent32
HP:0002017HP:0002013Vomiting1TIMM22 CL E G H2992817317OMIM:618851COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43; COXPD43
HP:0002017HP:0002013Vomiting1TIMMDC1 CL E G H513001321ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent1
HP:0002017HP:0002013Vomiting1TMEM126B CL E G H5586330883ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent4
HP:0002017HP:0002018Nausea1TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent131
HP:0002017HP:0002013Vomiting1TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 1.7
HP:0002017HP:0002018Nausea1TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 1.7
HP:0002017HP:0002013Vomiting1TNFRSF1A CL E G H713211916OMIM:142680Periodic fever, familial, autosomal dominant131
HP:0002017HP:0002013Vomiting1TNFRSF1A CL E G H713211916ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndromeHP:0040282 - Frequent131
HP:0002017HP:0002013Vomiting1TOM1 CL E G H1004311982OMIM:619510IMMUNODEFICIENCY 85 AND AUTOIMMUNITY; IMD85
HP:0002017HP:0002013Vomiting1TP53 CL E G H715711998OMIM:260500Papilloma of choroid plexus.911
HP:0002017HP:0002018Nausea1TP53 CL E G H715711998OMIM:260500Papilloma of choroid plexus.911
HP:0002017HP:0002013Vomiting1TREH CL E G H1118112266ORPHA:103909Trehalase deficiency2
HP:0002017HP:0002013Vomiting1TRMU CL E G H5568725481OMIM:613070Liver failure, infantile, transient.101
HP:0002017HP:0002013Vomiting1TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNF CL E G H45587481ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNH CL E G H45647487ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNK CL E G H45667489ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNL1 CL E G H45677490ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNL1 CL E G H45677490ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNQ CL E G H45727495ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNS1 CL E G H45747497ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNS2 CL E G H45757498ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNV CL E G H45777500ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TRNW CL E G H45787501ORPHA:550MELASHP:0040282 - Frequent
HP:0002017HP:0002013Vomiting1TRNW CL E G H45787501ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002017HP:0002013Vomiting1TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002017HP:0002013Vomiting1TXNRD2 CL E G H1058718155ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent85
HP:0002017HP:0002013Vomiting1TYMP CL E G H18903148OMIM:603041Mitochondrial DNA depletion syndrome 1 (mngie type).138
HP:0002017HP:0002013Vomiting1TYMP CL E G H18903148ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent138
HP:0002017HP:0002018Nausea1TYMP CL E G H18903148ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent138
HP:0002017HP:0002018Nausea1UCHL1 CL E G H734512513ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional21
HP:0002017HP:0002013Vomiting1UNC45A CL E G H5589830594OMIM:619377OSTEOOTOHEPATOENTERIC SYNDROME; OOHE
HP:0002017HP:0002013Vomiting1UQCC2 CL E G H8430021237OMIM:615824Mitochondrial complex III deficiency, nuclear type 77
HP:0002017HP:0002013Vomiting1UQCRC2 CL E G H738512586OMIM:615160Mitochondrial complex III deficiency, nuclear type 517
HP:0002017HP:0002018Nausea1VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent490
HP:0002017HP:0002018Nausea1VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent490
HP:0002017HP:0002018Nausea1VPS13C CL E G H5483223594ORPHA:2828Young-onset Parkinson diseaseHP:0040283 - Occasional8
HP:0002017HP:0002013Vomiting1YARS1 CL E G H856512840OMIM:619418NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2; IMNEPD2
HP:0002017HP:0002013Vomiting1ZEB2 CL E G H983914881OMIM:235730Mowat-Wilson syndrome.362
HP:0002017HP:0002013Vomiting1ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutation362
HP:0002017HP:0002013Vomiting1ZEB2 CL E G H983914881ORPHA:261537Mowat-Wilson syndrome due to monosomy 2q22362
HP:0002017HP:0002013Vomiting1ZFTA CL E G H6599828449ORPHA:251636EpendymomaHP:0040283 - Occasional
HP:0002017HP:0002013Vomiting1ZIC2 CL E G H754612873ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent34
HP:0002017HP:0002013Vomiting1ZIC2 CL E G H754612873ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional34
HP:0002017HP:0002013Vomiting1ZIC2 CL E G H754612873ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent34
HP:0002017HP:0002013Vomiting1ZIC2 CL E G H754612873ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent34
HP:0002017HP:0025089Feculent vomiting2 CL E G H
HP:0002017HP:0002572Episodic vomiting2ACADVL CL E G H3792OMIM:201475Very long-chain acyl-CoA dehydrogenase deficiency200
HP:0002017HP:0002587Projectile vomiting2AIMP1 CL E G H925510648OMIM:260600Leukodystrophy, hypomyelinating, 3.4
HP:0002017HP:0002572Episodic vomiting2ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiencyHP:0040283 - Occasional62
HP:0002017HP:0002572Episodic vomiting2ALG11 CL E G H44013832456ORPHA:280071ALG11-CDGHP:0040283 - Occasional41
HP:0002017HP:0002587Projectile vomiting2ANO1 CL E G H5510721625OMIM:620045
HP:0002017HP:0002572Episodic vomiting2ARG1 CL E G H383663OMIM:207800Argininemia31
HP:0002017HP:0002572Episodic vomiting2ATP6 CL E G H45087414ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2CCM2 CL E G H8360521708ORPHA:221061Familial cerebral cavernous malformationHP:0040283 - Occasional37
HP:0002017HP:0002572Episodic vomiting2CDC42BPB CL E G H95781738OMIM:619841
HP:0002017HP:0002572Episodic vomiting2CDK13 CL E G H86211733OMIM:617360Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder8
HP:0002017HP:0002572Episodic vomiting2CDK8 CL E G H10241779OMIM:618748INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA
HP:0002017HP:0002587Projectile vomiting2CLMP CL E G H7982724039OMIM:615237Congenital short bowel syndrome7
HP:0002017HP:0002572Episodic vomiting2COQ2 CL E G H2723525223OMIM:607426Coenzyme Q10 deficiency, primary, 154
HP:0002017HP:0002572Episodic vomiting2COQ2 CL E G H2723525223ORPHA:255249Leigh syndrome with nephrotic syndromeHP:0040282 - Frequent54
HP:0002017HP:0002572Episodic vomiting2COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyriaHP:0040282 - Frequent72
HP:0002017HP:0002572Episodic vomiting2CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2D2HGDH CL E G H72829428358OMIM:600721D-2-Hydroxyglutaric aciduria 1.102
HP:0002017HP:0002572Episodic vomiting2FAH CL E G H21843579OMIM:276700Tyrosinemia, type I107
HP:0002017HP:0002572Episodic vomiting2GAMT CL E G H25934136OMIM:612736Cerebral creatine deficiency syndrome 291
HP:0002017HP:0002572Episodic vomiting2GK CL E G H27104289OMIM:307030Glycerol kinase deficiency.13
HP:0002017HP:0002572Episodic vomiting2HMGCL CL E G H31555005ORPHA:203-hydroxy-3-methylglutaric aciduriaHP:0040282 - Frequent35
HP:0002017HP:0002572Episodic vomiting2HNRNPK CL E G H31905044ORPHA:352665Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletionHP:0040283 - Occasional8
HP:0002017HP:0002572Episodic vomiting2HNRNPK CL E G H31905044ORPHA:453504Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutationHP:0040283 - Occasional8
HP:0002017HP:0002572Episodic vomiting2HS3ST6 CL E G H6471114178OMIM:619367ANGIOEDEMA, HEREDITARY, 8; HAE8
HP:0002017HP:0002572Episodic vomiting2KRIT1 CL E G H8891573ORPHA:221061Familial cerebral cavernous malformationHP:0040283 - Occasional92
HP:0002017HP:0002572Episodic vomiting2LBX1 CL E G H1066016960OMIM:619483CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3; CCHS3
HP:0002017HP:0002572Episodic vomiting2NAXD CL E G H5573925576OMIM:618321Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2
HP:0002017HP:0002572Episodic vomiting2ND1 CL E G H45357455ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2ND2 CL E G H45367456ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2ND3 CL E G H45377458ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2ND4 CL E G H45387459ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2ND5 CL E G H45407461ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2ND6 CL E G H45417462ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2NEXMIF CL E G H34053329433OMIM:300912Mental retardation, X-linked 9852
HP:0002017HP:0002572Episodic vomiting2NFIX CL E G H47847788ORPHA:44798019p13.3 microduplication syndromeHP:0040283 - Occasional40
HP:0002017HP:0002572Episodic vomiting2NLRC4 CL E G H5848416412OMIM:616050AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC30
HP:0002017HP:0002572Episodic vomiting2NOTCH2NLC CL E G H10099671753924OMIM:603472NEURONAL INTRANUCLEAR INCLUSION DISEASE
HP:0002017HP:0002572Episodic vomiting2NSD1 CL E G H6432414234OMIM:117550Sotos syndrome 1544
HP:0002017HP:0002572Episodic vomiting2PDCD10 CL E G H112358761ORPHA:221061Familial cerebral cavernous malformationHP:0040283 - Occasional21
HP:0002017HP:0002572Episodic vomiting2PDSS2 CL E G H5710723041ORPHA:255249Leigh syndrome with nephrotic syndromeHP:0040282 - Frequent54
HP:0002017HP:0002572Episodic vomiting2PNPLA8 CL E G H5064028900OMIM:251950Mitochondrial myopathy with lactic acidosis.3
HP:0002017HP:0002572Episodic vomiting2SHANK3 CL E G H8535814294OMIM:606232Phelan-Mcdermid syndrome53
HP:0002017HP:0002572Episodic vomiting2SLC25A15 CL E G H1016610985OMIM:238970Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome.88
HP:0002017HP:0002572Episodic vomiting2SLC25A15 CL E G H1016610985ORPHA:415Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeHP:0040282 - Frequent88
HP:0002017HP:0002572Episodic vomiting2SLC5A6 CL E G H888411041OMIM:618973NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE; NERIB
HP:0002017HP:0002572Episodic vomiting2SUOX CL E G H682111460OMIM:272300SULFOCYSTEINURIA40
HP:0002017HP:0002587Projectile vomiting2TIMM22 CL E G H2992817317OMIM:618851COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43; COXPD43
HP:0002017HP:0002572Episodic vomiting2TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNK CL E G H45667489ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNL1 CL E G H45677490ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNV CL E G H45777500ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2TRNW CL E G H45787501ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002017HP:0002572Episodic vomiting2TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002017HP:0002572Episodic vomiting2UNC45A CL E G H5589830594OMIM:619377OSTEOOTOHEPATOENTERIC SYNDROME; OOHE
HP:0002017HP:0002572Episodic vomiting2UQCRC2 CL E G H738512586OMIM:615160Mitochondrial complex III deficiency, nuclear type 517
HP:0002017HP:0002572Episodic vomiting2ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutationHP:0040283 - Occasional362
HP:0002017HP:0002572Episodic vomiting2ZEB2 CL E G H983914881ORPHA:261537Mowat-Wilson syndrome due to monosomy 2q22HP:0040283 - Occasional362


Genes (533) :AASS ABCC6 ABCC8 ABCD1 ACAD8 ACADM ACADVL ACAT1 ACSF3 ACTG2 ACY1 ADNP AIMP1 AIP AKT1 ALAD ALDH18A1 ALDOB ALG11 ALG3 ALG8 ALG9 ALPL ALX4 AMN ANAPC1 ANG ANO1 ANXA11 APC AQP2 ARG1 ASL ASPA ASS1 ASXL1 ASXL3 ATP1A2 ATP1A3 ATP6 ATP6V0A4 ATP7A ATP7B ATRX ATXN2 AVP AVPR2 BAP1 BAZ1B BCKDHA BCKDHB BCL10 BCL7B BIRC3 BMPR1A BOLA3 BRAF BRCA1 BRCA2 BSND BTD BUD23 C4A C9ORF72 CACNA1A CACNA1D CARD8 CAV1 CCM2 CCN2 CCNF CCR1 CCR6 CD46 CD55 CDC42BPB CDC73 CDH23 CDK13 CDK8 CDKN1A CDKN1B CDKN2A CDKN2B CDKN2C CDON CFAP410 CFH CFI CHCHD10 CHMP2B CLCN2 CLCNKA CLCNKB CLIP2 CLMP COA8 COL1A1 COL4A5 COL4A6 COL5A1 COL5A2 COQ2 COX1 COX2 COX3 CPOX CPS1 CPT2 CTLA4 CTNNB1 CTNS CTRC CUBN CYC1 CYP11A1 CYP11B1 CYP11B2 CYP24A1 CYTB D2HGDH DAO DAXX DBH DBT DCTN1 DGAT1 DGUOK DHCR7 DISP1 DLD DLEC1 DLL1 DLST DNAJC30 DNAJC6 DNASE1L3 DNMT3A DOLK DYRK1A ECE1 EDN3 EDNRA EDNRB EGFR EIF4H ELN ELP1 ENPP1 EPAS1 EPCAM EPHA4 ERAP1 ERBB2 ERBB3 ERBB4 ESR1 ETFA ETFB ETFDH EWSR1 EXT2 F12 FAH FAN1 FARSB FAS FBLN5 FBP1 FGF8 FGFR1 FH FIG4 FKBP6 FLI1 FLNA FOCAD FOXH1 FOXP1 FOXP3 FOXRED1 FSHR FUS GALC GALE GALT GAMT GAN GAS1 GATA2 GDNF GFAP GFM2 GHSR GK GLA GLE1 GLI2 GLT8D1 GRB10 GTF2I GTF2IRD1 GTF2IRD2 HADH HELLPAR HFE HIBCH HLA-B HLA-DPA1 HLA-DPB1 HLA-DQA1 HLA-DQB1 HLA-DRB1 HLCS HMBS HMGCL HMGCS2 HNF4A HNRNPA1 HNRNPK HPRT1 HS3ST6 HSD3B2 HTRA2 IFNGR1 IGH IKZF1 IL10 IL12A IL12A-AS1 IL18BP IL23R IRAK1 IRF5 ITGA6 ITGB4 IVD KARS1 KCNA1 KCNJ1 KCNJ11 KCNJ5 KIAA0319L KIF1B KIT KLRC4 KMT2E KRAS KRIT1 KYNU LAMA3 LAMB3 LAMC2 LBX1 LIG3 LIMK1 LIPA LMOD1 LPL LRRK2 MALT1 MARS1 MATR3 MAX MC2R MCCC1 MCCC2 MDH2 MED12 MEFV MEN1 MET METTL27 MGME1 MLH1 MLH3 MLXIPL MLYCD MMAA MMAB MMUT MPI MPV17 MRAP MRPS7 MSH2 MSH6 MSX2 MTHFD1 MTRR MTTP MVK MYC MYH11 MYLK NAA10 NAGS NARS2 NAXD NBAS NCF1 ND1 ND2 ND3 ND4 ND5 ND6 NDUFA1 NDUFA11 NDUFA6 NDUFAF1 NDUFAF2 NDUFAF3 NDUFAF4 NDUFAF5 NDUFAF8 NDUFB10 NDUFB11 NDUFB3 NDUFB9 NDUFS1 NDUFS2 NDUFS3 NDUFS4 NDUFS6 NDUFS7 NDUFS8 NDUFV1 NDUFV2 NEFH NEK1 NEUROG3 NEXMIF NF1 NF2 NFIX NLRC4 NLRP3 NNT NODAL NOTCH2NLC NPPA NR3C2 NRTN NSD1 NUBPL OPLAH OPTN OTC OXCT1 PAH PALB2 PALLD PARK7 PCCA PCCB PDCD10 PDGFB PDGFRA PDSS2 PERCC1 PFN1 PGM1 PHGDH PHKA2 PHKB PHKG2 PIGY PIK3CA PINK1 PKHD1 PLCH1 PLEC PMM2 PMS1 PMS2 PNPLA8 PNPT1 PODXL POLG PON1 PON2 PON3 PPARGC1A PPM1D PPOX PRKN PRPH PRTN3 PSAP PTCH1 PTEN PTPN22 PYCR2 RAB27A RABL3 RANBP2 RARS1 RECQL4 RELA RET RFC2 RHBDF2 RNF6 RPS20 RRM2B RYR1 SAA1 SAR1B SCN2A SCN5A SCNN1A SCNN1B SCNN1G SDHA SDHAF2 SDHB SDHC SDHD SEMA3C SEMA3D SEMA4A SERPING1 SHANK3 SHH SI SIX3 SLC12A1 SLC12A3 SLC19A3 SLC1A3 SLC22A12 SLC22A5 SLC25A11 SLC25A13 SLC25A15 SLC25A4 SLC2A9 SLC37A4 SLC46A1 SLC5A1 SLC5A6 SLC6A8 SLC7A7 SMAD4 SMARCB1 SMARCE1 SMC1A SMO SMPD1 SNCA SOD1 SPINK1 SPP1 SPTBN1 SQSTM1 SREBF1 SRSF2 SSR4 ST3GAL5 STAG2 STAR STAT4 STIL STK11 STX1A STX3 SUCLG1 SUFU SUGCT SUOX SYK SYNJ1 SYT1 TAF15 TARDBP TBK1 TBL2 TCN2 TDGF1 TERT TET2 TGFBR2 TGIF1 TICAM1 TIMM22 TIMMDC1 TLR3 TLR4 TMEM126B TMEM127 TMEM270 TNF TNFRSF1A TOM1 TP53 TRAF3 TRAF7 TREH TREM2 TRMT5 TRMU TRNC TRNF TRNH TRNK TRNL1 TRNQ TRNS1 TRNS2 TRNV TRNW TXNRD2 TYMP UBAC2 UBQLN2 UCHL1 UNC13A UNC45A UNC93B1 UQCC2 UQCRC2 VAPB VCP VHL VPS13C VPS37D WT1 WWOX YARS1 ZEB2 ZFTA ZIC2

Diseases (342) :ORPHA:2203 ORPHA:51608 ORPHA:79134 ORPHA:388 ORPHA:79159 OMIM:201450 ORPHA:42 ORPHA:26793 OMIM:201475 OMIM:203750 ORPHA:134 ORPHA:289504 OMIM:614265 ORPHA:2241 OMIM:155310 ORPHA:137754 ORPHA:404448 OMIM:260600 ORPHA:2965 ORPHA:2495 ORPHA:100924 OMIM:612740 ORPHA:90348 OMIM:601162 OMIM:229600 ORPHA:469 ORPHA:280071 OMIM:613661 OMIM:601110 ORPHA:79325 OMIM:608104 ORPHA:79328 OMIM:241500 ORPHA:60015 ORPHA:35858 ORPHA:221008 ORPHA:803 OMIM:620045 ORPHA:99818 OMIM:125800 ORPHA:223 OMIM:207800 OMIM:207900 ORPHA:314911 OMIM:215700 ORPHA:97297 ORPHA:98849 OMIM:615485 ORPHA:2131 OMIM:602481 ORPHA:255210 OMIM:602722 ORPHA:565 OMIM:277900 ORPHA:847 OMIM:309580 ORPHA:100075 ORPHA:30925 OMIM:304800 ORPHA:904 OMIM:248600 ORPHA:52417 ORPHA:440437 OMIM:614299 OMIM:115150 ORPHA:54595 ORPHA:1333 ORPHA:168829 ORPHA:89938 OMIM:253260 ORPHA:117 ORPHA:71518 ORPHA:97 ORPHA:369929 OMIM:619079 ORPHA:220393 ORPHA:220402 OMIM:606721 ORPHA:221061 ORPHA:244242 OMIM:226300 OMIM:619841 ORPHA:99880 ORPHA:143 ORPHA:91347 OMIM:617360 OMIM:618748 ORPHA:652 ORPHA:93925 ORPHA:93924 ORPHA:93926 ORPHA:220386 ORPHA:404 ORPHA:358 OMIM:615237 ORPHA:436271 ORPHA:287 ORPHA:1018 OMIM:607426 ORPHA:255249 ORPHA:550 OMIM:540000 OMIM:121300 OMIM:618892 ORPHA:79273 OMIM:237300 OMIM:600649 OMIM:608836 ORPHA:900 ORPHA:33402 ORPHA:411629 ORPHA:411634 ORPHA:103918 OMIM:615453 ORPHA:168558 ORPHA:289548 ORPHA:403 OMIM:203400 ORPHA:556030 OMIM:143880 ORPHA:137675 OMIM:600721 ORPHA:230 OMIM:615863 OMIM:251880 OMIM:270400 ORPHA:2394 ORPHA:99977 ORPHA:29072 ORPHA:2828 ORPHA:36412 ORPHA:276621 OMIM:610768 ORPHA:464311 OMIM:157300 OMIM:616069 OMIM:223900 ORPHA:92050 ORPHA:144 OMIM:243180 OMIM:231680 ORPHA:83469 ORPHA:466926 OMIM:610618 OMIM:276700 OMIM:613658 ORPHA:348 ORPHA:370348 OMIM:300048 OMIM:619991 ORPHA:37042 ORPHA:2609 ORPHA:64739 OMIM:608115 ORPHA:206436 OMIM:245200 OMIM:230350 ORPHA:79239 OMIM:230400 OMIM:612736 OMIM:256850 ORPHA:3226 ORPHA:363717 ORPHA:565624 ORPHA:314811 OMIM:307030 ORPHA:324 OMIM:301500 ORPHA:96182 ORPHA:71212 OMIM:176200 ORPHA:88639 ORPHA:36426 OMIM:212750 ORPHA:79242 OMIM:253270 ORPHA:79276 OMIM:176000 ORPHA:20 OMIM:246450 OMIM:605911 ORPHA:263455 ORPHA:352665 ORPHA:453504 OMIM:300322 OMIM:619367 ORPHA:90791 OMIM:618549 ORPHA:93552 ORPHA:79403 ORPHA:158684 OMIM:243500 OMIM:619147 ORPHA:37612 OMIM:241200 ORPHA:251274 ORPHA:79455 ORPHA:44890 OMIM:618512 OMIM:236800 ORPHA:79404 OMIM:619483 ORPHA:298 ORPHA:75234 OMIM:278000 ORPHA:75233 OMIM:238600 OMIM:615486 ORPHA:361 OMIM:210200 OMIM:210210 OMIM:301068 ORPHA:342 OMIM:249100 OMIM:615084 ORPHA:352447 OMIM:248360 OMIM:251100 OMIM:251110 OMIM:251000 ORPHA:79312 ORPHA:289916 OMIM:602579 ORPHA:79319 OMIM:256810 OMIM:617872 OMIM:617780 ORPHA:2169 ORPHA:14 OMIM:260920 OMIM:610377 ORPHA:543 OMIM:300855 ORPHA:927 OMIM:237310 OMIM:618321 OMIM:616483 OMIM:618226 OMIM:252010 OMIM:618225 OMIM:610370 ORPHA:83620 OMIM:300912 ORPHA:447980 OMIM:616050 ORPHA:1451 ORPHA:47045 OMIM:603472 ORPHA:1344 OMIM:177735 OMIM:117550 OMIM:260005 OMIM:311250 OMIM:245050 ORPHA:79254 OMIM:606054 OMIM:614921 ORPHA:79351 ORPHA:264580 ORPHA:79240 OMIM:616809 ORPHA:53035 OMIM:212065 ORPHA:79318 OMIM:251950 OMIM:608703 ORPHA:101111 OMIM:603041 OMIM:203700 OMIM:617450 ORPHA:79473 ORPHA:65285 ORPHA:481152 ORPHA:79477 ORPHA:88619 ORPHA:438114 ORPHA:221016 ORPHA:251636 OMIM:142623 ORPHA:2198 OMIM:612075 ORPHA:466650 ORPHA:85445 ORPHA:71 OMIM:246700 OMIM:618924 ORPHA:171876 OMIM:264350 ORPHA:100093 OMIM:106100 ORPHA:100050 ORPHA:48652 OMIM:606232 ORPHA:35122 OMIM:601678 OMIM:263800 OMIM:607483 ORPHA:209967 OMIM:612656 ORPHA:94088 OMIM:212140 ORPHA:158 ORPHA:247585 ORPHA:415 OMIM:238970 OMIM:615418 OMIM:619525 ORPHA:90045 ORPHA:35710 OMIM:618973 OMIM:300352 OMIM:222700 ORPHA:470 ORPHA:99966 OMIM:257200 OMIM:619475 ORPHA:370927 OMIM:609056 ORPHA:2869 OMIM:619445 ORPHA:17 OMIM:231690 OMIM:272300 OMIM:619381 ORPHA:522077 ORPHA:1930 OMIM:275350 OMIM:618851 OMIM:142680 ORPHA:32960 OMIM:619510 OMIM:260500 ORPHA:103909 OMIM:616539 OMIM:613070 OMIM:619377 OMIM:615824 OMIM:615160 OMIM:619418 OMIM:235730 ORPHA:261552 ORPHA:261537
 

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