Human Phenotype Ontology 
Grandparent Node:
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Abdominal symptom (HP:0011458)help
Parent Node:
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Nausea and vomiting (HP:0002017)help
..Starting node
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Vomiting (HP:0002013)help
Term ID: 2013
Name: Vomiting
Synonym: Emesis; Throwing up; Vomiting
Definition: Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic contractions.
Comments:
Reference: HP:0002013
Genes and Diseases:
 
       Child Nodes:
........expandEpisodic vomiting (HP:0002572) help
........expandProjectile vomiting (HP:0002587) help
........expandFeculent vomiting (HP:0025089) help

 Sister Nodes: 
..expandNausea (HP:0002018) 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:0002013HP:0002013Vomiting0AASS CL E G H1015717366ORPHA:2203HyperlysinemiaHP:0040283 - Occasional15
HP:0002013HP:0002013Vomiting0ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancyHP:0040283 - Occasional415
HP:0002013HP:0002013Vomiting0ABCC8 CL E G H683359ORPHA:79134DEND syndromeHP:0040283 - Occasional245
HP:0002013HP:0002013Vomiting0ACAD8 CL E G H2703487ORPHA:79159Isobutyryl-CoA dehydrogenase deficiencyHP:0040283 - Occasional58
HP:0002013HP:0002013Vomiting0ACADM CL E G H3489OMIM:201450Acyl-Coa dehydrogenase, medium-chain, deficiency of.197
HP:0002013HP:0002013Vomiting0ACADM CL E G H3489ORPHA:42Medium chain acyl-CoA dehydrogenase deficiencyHP:0040282 - Frequent197
HP:0002013HP:0002013Vomiting0ACADVL CL E G H3792ORPHA:26793Very long chain acyl-CoA dehydrogenase deficiencyHP:0040284 - Very rare200
HP:0002013HP:0002013Vomiting0ACADVL CL E G H3792OMIM:201475Very long-chain acyl-CoA dehydrogenase deficiency200
HP:0002013HP:0002013Vomiting0ACAT1 CL E G H3893OMIM:203750Alpha-Methylacetoacetic aciduria.91
HP:0002013HP:0002013Vomiting0ACAT1 CL E G H3893ORPHA:134Beta-ketothiolase deficiencyHP:0040281 - Very frequent91
HP:0002013HP:0002013Vomiting0ACSF3 CL E G H19732227288ORPHA:289504Combined malonic and methylmalonic acidemiaHP:0040283 - Occasional68
HP:0002013HP:0002013Vomiting0ACSF3 CL E G H19732227288OMIM:614265Combined malonic and methylmalonic aciduria.68
HP:0002013HP:0002013Vomiting0ACTG2 CL E G H72145OMIM:155310Visceral myopathy 1.23
HP:0002013HP:0002013Vomiting0ACY1 CL E G H95177ORPHA:137754Neurological conditions associated with aminoacylase 1 deficiencyHP:0040283 - Occasional13
HP:0002013HP:0002013Vomiting0ADNP CL E G H2339415766ORPHA:404448ADNP syndromeHP:0040283 - Occasional47
HP:0002013HP:0002013Vomiting0AIMP1 CL E G H925510648OMIM:260600Leukodystrophy, hypomyelinating, 34
HP:0002013HP:0002013Vomiting0AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040282 - Frequent95
HP:0002013HP:0002013Vomiting0ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiency62
HP:0002013HP:0002013Vomiting0ALAD CL E G H210395OMIM:612740Porphyria, acute hepatic.62
HP:0002013HP:0002013Vomiting0ALDH18A1 CL E G H58329722ORPHA:90348Autosomal dominant cutis laxa89
HP:0002013HP:0002013Vomiting0ALDH18A1 CL E G H58329722OMIM:601162Spastic paraplegia 9A, autosomal dominant.89
HP:0002013HP:0002013Vomiting0ALDOB CL E G H229417OMIM:229600Fructose intolerance, hereditary.73
HP:0002013HP:0002013Vomiting0ALDOB CL E G H229417ORPHA:469Hereditary fructose intoleranceHP:0040283 - Occasional73
HP:0002013HP:0002013Vomiting0ALG11 CL E G H44013832456ORPHA:280071ALG11-CDG41
HP:0002013HP:0002013Vomiting0ALG11 CL E G H44013832456OMIM:613661Congenital disorder of glycosylation, type Ip.41
HP:0002013HP:0002013Vomiting0ALG3 CL E G H1019523056OMIM:601110Congenital disorder of glycosylation, type Id.37
HP:0002013HP:0002013Vomiting0ALG8 CL E G H7905323161ORPHA:79325ALG8-CDGHP:0040283 - Occasional46
HP:0002013HP:0002013Vomiting0ALG8 CL E G H7905323161OMIM:608104Congenital disorder of glycosylation, type Ih.46
HP:0002013HP:0002013Vomiting0ALG9 CL E G H7979615672ORPHA:79328ALG9-CDGHP:0040283 - Occasional93
HP:0002013HP:0002013Vomiting0ALPL CL E G H249438OMIM:241500Hypophosphatasia, infantile.126
HP:0002013HP:0002013Vomiting0ALX4 CL E G H60529450ORPHA:60015Enlarged parietal foraminaHP:0040283 - Occasional132
HP:0002013HP:0002013Vomiting0AMN CL E G H8169314604ORPHA:35858Imerslund-Gräsbeck syndromeHP:0040283 - Occasional25
HP:0002013HP:0002013Vomiting0ANAPC1 CL E G H6468219988ORPHA:221008Rothmund-Thomson syndrome type 1HP:0040283 - Occasional2
HP:0002013HP:0002013Vomiting0ANO1 CL E G H5510721625OMIM:620045
HP:0002013HP:0002013Vomiting0APC CL E G H324583ORPHA:99818Turcot syndrome with polyposisHP:0040283 - Occasional3179
HP:0002013HP:0002013Vomiting0AQP2 CL E G H359634OMIM:125800Diabetes insipidus, nephrogenic, 2.75
HP:0002013HP:0002013Vomiting0ARG1 CL E G H383663OMIM:207800Argininemia.31
HP:0002013HP:0002013Vomiting0ASL CL E G H435746OMIM:207900Argininosuccinic aciduria.81
HP:0002013HP:0002013Vomiting0ASPA CL E G H443756ORPHA:314911Severe Canavan diseaseHP:0040282 - Frequent48
HP:0002013HP:0002013Vomiting0ASS1 CL E G H445758OMIM:215700Citrullinemia, classic.119
HP:0002013HP:0002013Vomiting0ASXL1 CL E G H17102318318ORPHA:97297Bohring-Opitz syndromeHP:0040282 - Frequent145
HP:0002013HP:0002013Vomiting0ASXL3 CL E G H8081629357OMIM:615485BAINBRIDGE-ROPERS SYNDROME; BRPS49
HP:0002013HP:0002013Vomiting0ATP1A2 CL E G H477800ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent239
HP:0002013HP:0002013Vomiting0ATP1A3 CL E G H478801ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent150
HP:0002013HP:0002013Vomiting0ATP6 CL E G H45087414ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ATP6V0A4 CL E G H50617866OMIM:602722RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR64
HP:0002013HP:0002013Vomiting0ATP7B CL E G H540870OMIM:277900Wilson disease315
HP:0002013HP:0002013Vomiting0ATRX CL E G H546886OMIM:309580Mental retardation-hypotonic facies syndrome, X-linked, 1.169
HP:0002013HP:0002013Vomiting0AVP CL E G H551894ORPHA:30925Hereditary central diabetes insipidusHP:0040282 - Frequent22
HP:0002013HP:0002013Vomiting0AVPR2 CL E G H554897OMIM:304800Diabetes insipidus, nephrogenic, X-linked.67
HP:0002013HP:0002013Vomiting0BCKDHA CL E G H593986OMIM:248600Maple syrup urine disease.120
HP:0002013HP:0002013Vomiting0BCKDHB CL E G H594987OMIM:248600Maple syrup urine disease.162
HP:0002013HP:0002013Vomiting0BOLA3 CL E G H38896224415OMIM:614299Multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia.14
HP:0002013HP:0002013Vomiting0BRAF CL E G H6731097OMIM:115150Cardiofaciocutaneous syndrome 1.276
HP:0002013HP:0002013Vomiting0BSND CL E G H780916512ORPHA:89938Infantile Bartter syndrome with sensorineural deafnessHP:0040283 - Occasional53
HP:0002013HP:0002013Vomiting0BTD CL E G H6861122OMIM:253260Biotinidase deficiencymultiple carboxylase deficiency, late-onset.223
HP:0002013HP:0002013Vomiting0CACNA1A CL E G H7731388ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent449
HP:0002013HP:0002013Vomiting0CACNA1A CL E G H7731388ORPHA:71518Benign paroxysmal torticollis of infancyHP:0040282 - Frequent449
HP:0002013HP:0002013Vomiting0CARD8 CL E G H2290017057OMIM:619079INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 30; IBD301
HP:0002013HP:0002013Vomiting0CAV1 CL E G H8571527OMIM:606721Lipodystrophy, familial partial, type 711
HP:0002013HP:0002013Vomiting0CCM2 CL E G H8360521708ORPHA:221061Familial cerebral cavernous malformation37
HP:0002013HP:0002013Vomiting0CD46 CL E G H41796953ORPHA:244242HELLP syndromeHP:0040283 - Occasional39
HP:0002013HP:0002013Vomiting0CD55 CL E G H16042665OMIM:226300Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy.9
HP:0002013HP:0002013Vomiting0CDC42BPB CL E G H95781738OMIM:619841
HP:0002013HP:0002013Vomiting0CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040282 - Frequent636
HP:0002013HP:0002013Vomiting0CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040282 - Frequent636
HP:0002013HP:0002013Vomiting0CDK13 CL E G H86211733OMIM:617360Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder8
HP:0002013HP:0002013Vomiting0CDK8 CL E G H10241779OMIM:618748INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA
HP:0002013HP:0002013Vomiting0CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional2
HP:0002013HP:0002013Vomiting0CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional102
HP:0002013HP:0002013Vomiting0CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional1
HP:0002013HP:0002013Vomiting0CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0CDON CL E G H5093717104ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent200
HP:0002013HP:0002013Vomiting0CDON CL E G H5093717104ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional200
HP:0002013HP:0002013Vomiting0CDON CL E G H5093717104ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent200
HP:0002013HP:0002013Vomiting0CDON CL E G H5093717104ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent200
HP:0002013HP:0002013Vomiting0CFH CL E G H30754883ORPHA:244242HELLP syndromeHP:0040283 - Occasional86
HP:0002013HP:0002013Vomiting0CFI CL E G H34265394ORPHA:244242HELLP syndromeHP:0040283 - Occasional57
HP:0002013HP:0002013Vomiting0CLCNKA CL E G H11872026ORPHA:89938Infantile Bartter syndrome with sensorineural deafnessHP:0040283 - Occasional9
HP:0002013HP:0002013Vomiting0CLCNKB CL E G H11882027ORPHA:89938Infantile Bartter syndrome with sensorineural deafnessHP:0040283 - Occasional27
HP:0002013HP:0002013Vomiting0CLMP CL E G H7982724039OMIM:615237Congenital short bowel syndromeHP:0040283 - Occasional7
HP:0002013HP:0002013Vomiting0COA8 CL E G H8433420492ORPHA:436271Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathyHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0COL1A1 CL E G H12772197ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent373
HP:0002013HP:0002013Vomiting0COL4A5 CL E G H12872207ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent678
HP:0002013HP:0002013Vomiting0COL4A6 CL E G H12882208ORPHA:1018X-linked Alport syndrome-diffuse leiomyomatosisHP:0040282 - Frequent18
HP:0002013HP:0002013Vomiting0COL5A1 CL E G H12892209ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent660
HP:0002013HP:0002013Vomiting0COL5A2 CL E G H12902210ORPHA:287Classical Ehlers-Danlos syndromeHP:0040282 - Frequent325
HP:0002013HP:0002013Vomiting0COQ2 CL E G H2723525223OMIM:607426Coenzyme Q10 deficiency, primary, 154
HP:0002013HP:0002013Vomiting0COQ2 CL E G H2723525223ORPHA:255249Leigh syndrome with nephrotic syndrome54
HP:0002013HP:0002013Vomiting0COX1 CL E G H45127419ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0COX2 CL E G H45137421ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0COX3 CL E G H45147422ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0CPOX CL E G H13712321OMIM:121300Coproporphyria.72
HP:0002013HP:0002013Vomiting0CPOX CL E G H13712321OMIM:618892Harderoporphyria.72
HP:0002013HP:0002013Vomiting0CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyria72
HP:0002013HP:0002013Vomiting0CPS1 CL E G H13732323OMIM:237300Carbamoyl phosphate synthetase I deficiency, hyperammonemia due to.124
HP:0002013HP:0002013Vomiting0CPT2 CL E G H13762330OMIM:600649Carnitine palmitoyltransferase II deficiency, infantile.101
HP:0002013HP:0002013Vomiting0CPT2 CL E G H13762330OMIM:608836Carnitine palmitoyltransferase II deficiency, lethal neonatal101
HP:0002013HP:0002013Vomiting0CTNNB1 CL E G H14992514ORPHA:33402Pediatric hepatocellular carcinomaHP:0040282 - Frequent88
HP:0002013HP:0002013Vomiting0CTNS CL E G H14972518ORPHA:411629Infantile nephropathic cystinosisHP:0040281 - Very frequent178
HP:0002013HP:0002013Vomiting0CTNS CL E G H14972518ORPHA:411634Juvenile nephropathic cystinosisHP:0040282 - Frequent178
HP:0002013HP:0002013Vomiting0CTRC CL E G H113302523ORPHA:103918Tropical pancreatitis39
HP:0002013HP:0002013Vomiting0CUBN CL E G H80292548ORPHA:35858Imerslund-Gräsbeck syndromeHP:0040283 - Occasional273
HP:0002013HP:0002013Vomiting0CYC1 CL E G H15372579OMIM:615453Mitochondrial complex III deficiency, nuclear type 612
HP:0002013HP:0002013Vomiting0CYP11A1 CL E G H15832590ORPHA:16855846,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiencyHP:0040281 - Very frequent31
HP:0002013HP:0002013Vomiting0CYP11A1 CL E G H15832590ORPHA:289548Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiencyHP:0040281 - Very frequent31
HP:0002013HP:0002013Vomiting0CYP11B2 CL E G H15852592OMIM:203400Corticosterone methyloxidase type I deficiency.73
HP:0002013HP:0002013Vomiting0CYP11B2 CL E G H15852592ORPHA:556030Early-onset familial hypoaldosteronismHP:0040282 - Frequent73
HP:0002013HP:0002013Vomiting0CYP24A1 CL E G H15912602OMIM:143880Hypercalcemia, infantile, 1.73
HP:0002013HP:0002013Vomiting0CYTB CL E G H45197427ORPHA:137675Histiocytoid cardiomyopathyHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0D2HGDH CL E G H72829428358OMIM:600721D-2-Hydroxyglutaric aciduria 1102
HP:0002013HP:0002013Vomiting0DBH CL E G H16212689ORPHA:230Dopamine beta-hydroxylase deficiencyHP:0040283 - Occasional80
HP:0002013HP:0002013Vomiting0DBT CL E G H16292698OMIM:248600Maple syrup urine disease.156
HP:0002013HP:0002013Vomiting0DGAT1 CL E G H86942843OMIM:615863Diarrhea 7, protein-losing Enteropathy type.9
HP:0002013HP:0002013Vomiting0DGUOK CL E G H17162858OMIM:251880Mitochondrial DNA depletion syndrome 3 (hepatocerebral type).57
HP:0002013HP:0002013Vomiting0DHCR7 CL E G H17172860OMIM:270400Smith-Lemli-Opitz syndrome159
HP:0002013HP:0002013Vomiting0DISP1 CL E G H8497619711ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent22
HP:0002013HP:0002013Vomiting0DISP1 CL E G H8497619711ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional22
HP:0002013HP:0002013Vomiting0DISP1 CL E G H8497619711ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent22
HP:0002013HP:0002013Vomiting0DISP1 CL E G H8497619711ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent22
HP:0002013HP:0002013Vomiting0DLD CL E G H17382898ORPHA:2394Pyruvate dehydrogenase E3 deficiencyHP:0040281 - Very frequent89
HP:0002013HP:0002013Vomiting0DLL1 CL E G H285142908ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent3
HP:0002013HP:0002013Vomiting0DLL1 CL E G H285142908ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional3
HP:0002013HP:0002013Vomiting0DLL1 CL E G H285142908ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent3
HP:0002013HP:0002013Vomiting0DLL1 CL E G H285142908ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent3
HP:0002013HP:0002013Vomiting0DOLK CL E G H2284523406OMIM:610768Congenital disorder of glycosylation, type Im55
HP:0002013HP:0002013Vomiting0DYRK1A CL E G H18593091ORPHA:464311Intellectual disability syndrome due to a DYRK1A point mutationHP:0040283 - Occasional134
HP:0002013HP:0002013Vomiting0EDNRA CL E G H19093179OMIM:157300Migraine with or without aura, susceptibility to, 1.3
HP:0002013HP:0002013Vomiting0EGFR CL E G H19563236OMIM:616069Inflammatory skin and bowel disease, neonatal, 2.257
HP:0002013HP:0002013Vomiting0ELN CL E G H20063327ORPHA:90348Autosomal dominant cutis laxa172
HP:0002013HP:0002013Vomiting0ELP1 CL E G H85185959OMIM:223900Neuropathy, hereditary sensory and autonomic, type III.133
HP:0002013HP:0002013Vomiting0ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancyHP:0040283 - Occasional151
HP:0002013HP:0002013Vomiting0EPCAM CL E G H407211529ORPHA:92050Congenital tufting enteropathyHP:0040284 - Very rare170
HP:0002013HP:0002013Vomiting0ERBB3 CL E G H20653431OMIM:243180Visceral neuropathy, familial, autosomal recessive.12
HP:0002013HP:0002013Vomiting0ESR1 CL E G H20993467OMIM:157300Migraine with or without aura, susceptibility to, 1.13
HP:0002013HP:0002013Vomiting0ETFA CL E G H21083481OMIM:231680Multiple acyl-coa dehydrogenase deficiency.37
HP:0002013HP:0002013Vomiting0ETFB CL E G H21093482OMIM:231680Multiple acyl-coa dehydrogenase deficiency.27
HP:0002013HP:0002013Vomiting0ETFDH CL E G H21103483OMIM:231680Multiple acyl-coa dehydrogenase deficiency.77
HP:0002013HP:0002013Vomiting0F12 CL E G H21613530OMIM:610618ANGIOEDEMA, HEREDITARY, TYPE III; HAE328
HP:0002013HP:0002013Vomiting0FAH CL E G H21843579OMIM:276700Tyrosinemia, type I107
HP:0002013HP:0002013Vomiting0FARSB CL E G H1005617800OMIM:613658Rajab interstitial lung disease with brain calcifications
HP:0002013HP:0002013Vomiting0FBLN5 CL E G H105163602ORPHA:90348Autosomal dominant cutis laxa63
HP:0002013HP:0002013Vomiting0FBP1 CL E G H22033606ORPHA:348Fructose-1,6-bisphosphatase deficiencyHP:0040282 - Frequent64
HP:0002013HP:0002013Vomiting0FGF8 CL E G H22533686ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent17
HP:0002013HP:0002013Vomiting0FGF8 CL E G H22533686ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional17
HP:0002013HP:0002013Vomiting0FGF8 CL E G H22533686ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent17
HP:0002013HP:0002013Vomiting0FGF8 CL E G H22533686ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent17
HP:0002013HP:0002013Vomiting0FGFR1 CL E G H22603688ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional172
HP:0002013HP:0002013Vomiting0FGFR1 CL E G H22603688ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent172
HP:0002013HP:0002013Vomiting0FLNA CL E G H23163754OMIM:300048Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked.493
HP:0002013HP:0002013Vomiting0FOCAD CL E G H5491423377OMIM:6199913
HP:0002013HP:0002013Vomiting0FOXH1 CL E G H89283814ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent48
HP:0002013HP:0002013Vomiting0FOXH1 CL E G H89283814ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional48
HP:0002013HP:0002013Vomiting0FOXH1 CL E G H89283814ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent48
HP:0002013HP:0002013Vomiting0FOXH1 CL E G H89283814ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent48
HP:0002013HP:0002013Vomiting0FOXP3 CL E G H509436106ORPHA:37042Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndromeHP:0040283 - Occasional32
HP:0002013HP:0002013Vomiting0FOXRED1 CL E G H5557226927ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent61
HP:0002013HP:0002013Vomiting0GALC CL E G H25814115ORPHA:206436Infantile Krabbe diseaseHP:0040283 - Occasional160
HP:0002013HP:0002013Vomiting0GALC CL E G H25814115OMIM:245200Krabbe disease.160
HP:0002013HP:0002013Vomiting0GALE CL E G H25824116OMIM:230350Galactose epimerase deficiency.52
HP:0002013HP:0002013Vomiting0GALT CL E G H25924135ORPHA:79239Classic galactosemiaHP:0040282 - Frequent351
HP:0002013HP:0002013Vomiting0GALT CL E G H25924135OMIM:230400GALACTOSEMIA.351
HP:0002013HP:0002013Vomiting0GAMT CL E G H25934136OMIM:612736Cerebral creatine deficiency syndrome 291
HP:0002013HP:0002013Vomiting0GAN CL E G H81394137OMIM:256850Giant axonal neuropathy 1, autosomal recessive121
HP:0002013HP:0002013Vomiting0GAS1 CL E G H26194165ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent2
HP:0002013HP:0002013Vomiting0GAS1 CL E G H26194165ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional2
HP:0002013HP:0002013Vomiting0GAS1 CL E G H26194165ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent2
HP:0002013HP:0002013Vomiting0GAS1 CL E G H26194165ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent2
HP:0002013HP:0002013Vomiting0GFAP CL E G H26704235ORPHA:363717Alexander disease type I188
HP:0002013HP:0002013Vomiting0GFM2 CL E G H8434029682ORPHA:565624Combined oxidative phosphorylation defect type 39HP:0040283 - Occasional43
HP:0002013HP:0002013Vomiting0GHSR CL E G H26934267ORPHA:314811Short stature due to GHSR deficiencyHP:0040281 - Very frequent37
HP:0002013HP:0002013Vomiting0GK CL E G H27104289OMIM:307030Glycerol kinase deficiency13
HP:0002013HP:0002013Vomiting0GLA CL E G H27174296OMIM:301500Fabry disease.291
HP:0002013HP:0002013Vomiting0GLI2 CL E G H27364318ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent173
HP:0002013HP:0002013Vomiting0GLI2 CL E G H27364318ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional173
HP:0002013HP:0002013Vomiting0GLI2 CL E G H27364318ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent173
HP:0002013HP:0002013Vomiting0GLI2 CL E G H27364318ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent173
HP:0002013HP:0002013Vomiting0GRB10 CL E G H28874564ORPHA:96182Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7HP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0HADH CL E G H30334799ORPHA:71212Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiencyHP:0040281 - Very frequent41
HP:0002013HP:0002013Vomiting0HELLPAR CL E G H10110169243984ORPHA:244242HELLP syndromeHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0HFE CL E G H30774886OMIM:176200Porphyria variegata.38
HP:0002013HP:0002013Vomiting0HIBCH CL E G H262754908ORPHA:88639Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiencyHP:0040281 - Very frequent32
HP:0002013HP:0002013Vomiting0HLA-DQA1 CL E G H31174942OMIM:212750Celiac disease, susceptibility to, 1.
HP:0002013HP:0002013Vomiting0HLA-DQB1 CL E G H31194944OMIM:212750Celiac disease, susceptibility to, 1.
HP:0002013HP:0002013Vomiting0HLCS CL E G H31414976OMIM:253270Holocarboxylase synthetase deficiency.148
HP:0002013HP:0002013Vomiting0HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent.81
HP:0002013HP:0002013Vomiting0HMGCL CL E G H31555005ORPHA:203-hydroxy-3-methylglutaric aciduria35
HP:0002013HP:0002013Vomiting0HMGCL CL E G H31555005OMIM:2464503-Hydroxy-3-Methylglutaryl-Coa lyase deficiency.35
HP:0002013HP:0002013Vomiting0HMGCS2 CL E G H31585008OMIM:6059113-Hydroxy-3-Methylglutaryl-Coa synthase-2 deficiency.42
HP:0002013HP:0002013Vomiting0HNF4A CL E G H31725024ORPHA:263455Hyperinsulinism due to HNF4A deficiencyHP:0040282 - Frequent138
HP:0002013HP:0002013Vomiting0HNRNPK CL E G H31905044ORPHA:352665Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion8
HP:0002013HP:0002013Vomiting0HNRNPK CL E G H31905044ORPHA:453504Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation8
HP:0002013HP:0002013Vomiting0HPRT1 CL E G H32515157OMIM:300322Lesch-Nyhan syndrome.76
HP:0002013HP:0002013Vomiting0HS3ST6 CL E G H6471114178OMIM:619367ANGIOEDEMA, HEREDITARY, 8; HAE8
HP:0002013HP:0002013Vomiting0HSD3B2 CL E G H32845218ORPHA:90791Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiencyHP:0040282 - Frequent34
HP:0002013HP:0002013Vomiting0IRAK1 CL E G H36546112ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0ITGB4 CL E G H36916158ORPHA:158684Epidermolysis bullosa simplex with pyloric atresiaHP:0040282 - Frequent124
HP:0002013HP:0002013Vomiting0IVD CL E G H37126186OMIM:243500Isovaleric acidemia.105
HP:0002013HP:0002013Vomiting0KARS1 CL E G H37356215OMIM:619147LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS; LEPID
HP:0002013HP:0002013Vomiting0KCNJ1 CL E G H37586255OMIM:241200Bartter syndrome, antenatal, type 2.51
HP:0002013HP:0002013Vomiting0KCNJ11 CL E G H37676257ORPHA:79134DEND syndromeHP:0040283 - Occasional127
HP:0002013HP:0002013Vomiting0KIT CL E G H38156342ORPHA:79455Cutaneous mastocytoma327
HP:0002013HP:0002013Vomiting0KMT2E CL E G H5590418541OMIM:618512O'donnell-Luria-Rodan syndrome.1
HP:0002013HP:0002013Vomiting0KRIT1 CL E G H8891573ORPHA:221061Familial cerebral cavernous malformation92
HP:0002013HP:0002013Vomiting0KYNU CL E G H89426469OMIM:236800HYDROXYKYNURENINURIA5
HP:0002013HP:0002013Vomiting0LAMA3 CL E G H39096483ORPHA:79404Severe generalized junctional epidermolysis bullosaHP:0040283 - Occasional116
HP:0002013HP:0002013Vomiting0LAMB3 CL E G H39146490ORPHA:79404Severe generalized junctional epidermolysis bullosaHP:0040283 - Occasional167
HP:0002013HP:0002013Vomiting0LAMC2 CL E G H39186493ORPHA:79404Severe generalized junctional epidermolysis bullosaHP:0040283 - Occasional135
HP:0002013HP:0002013Vomiting0LBX1 CL E G H1066016960OMIM:619483CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3; CCHS3
HP:0002013HP:0002013Vomiting0LIG3 CL E G H39806600ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent1
HP:0002013HP:0002013Vomiting0LIPA CL E G H39886617OMIM:278000Lysosomal acid lipase deficiency73
HP:0002013HP:0002013Vomiting0LPL CL E G H40236677OMIM:238600Type I hyperlipoproteinemia.106
HP:0002013HP:0002013Vomiting0MARS1 CL E G H41416898OMIM:615486Interstitial lung and liver disease
HP:0002013HP:0002013Vomiting0MC2R CL E G H41586930ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent94
HP:0002013HP:0002013Vomiting0MCCC1 CL E G H569226936OMIM:2102003-Methylcrotonyl-CoA carboxylase 1 deficiency.81
HP:0002013HP:0002013Vomiting0MCCC2 CL E G H640876937OMIM:2102103-Methylcrotonyl-CoA carboxylase 2 deficiency.77
HP:0002013HP:0002013Vomiting0MED12 CL E G H996811957OMIM:301068HARDIKAR SYNDROME; HDKR228
HP:0002013HP:0002013Vomiting0MEFV CL E G H42106998OMIM:249100Familial Mediterranean fever, AR281
HP:0002013HP:0002013Vomiting0MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional462
HP:0002013HP:0002013Vomiting0MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040282 - Frequent462
HP:0002013HP:0002013Vomiting0MET CL E G H42337029ORPHA:33402Pediatric hepatocellular carcinomaHP:0040282 - Frequent375
HP:0002013HP:0002013Vomiting0MLYCD CL E G H234177150OMIM:248360Malonyl-CoA decarboxylase deficiency.80
HP:0002013HP:0002013Vomiting0MMAA CL E G H16678518871OMIM:251100Methylmalonic aciduria, Cbla type.113
HP:0002013HP:0002013Vomiting0MMAB CL E G H32662519331OMIM:251110Methylmalonic aciduria, Cblb type.127
HP:0002013HP:0002013Vomiting0MMUT CL E G H45947526OMIM:251000Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency.
HP:0002013HP:0002013Vomiting0MPI CL E G H43517216OMIM:602579Congenital disorder of glycosylation, type Ib.51
HP:0002013HP:0002013Vomiting0MPI CL E G H43517216ORPHA:79319MPI-CDGHP:0040282 - Frequent51
HP:0002013HP:0002013Vomiting0MPV17 CL E G H43587224OMIM:256810Navajo neurohepatopathy.56
HP:0002013HP:0002013Vomiting0MRAP CL E G H562461304ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent26
HP:0002013HP:0002013Vomiting0MRPS7 CL E G H5108114499OMIM:617872Combined oxidative phosphorylation deficiency 34.12
HP:0002013HP:0002013Vomiting0MSX2 CL E G H44887392ORPHA:60015Enlarged parietal foraminaHP:0040283 - Occasional45
HP:0002013HP:0002013Vomiting0MTHFD1 CL E G H45227432OMIM:617780Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia.5
HP:0002013HP:0002013Vomiting0MTRR CL E G H45527473ORPHA:2169Methylcobalamin deficiency type cblEHP:0040282 - Frequent88
HP:0002013HP:0002013Vomiting0MTTP CL E G H45477467ORPHA:14AbetalipoproteinemiaHP:0040283 - Occasional81
HP:0002013HP:0002013Vomiting0MVK CL E G H45987530OMIM:260920Hyper-Igd syndrome150
HP:0002013HP:0002013Vomiting0MVK CL E G H45987530OMIM:610377Mevalonic aciduria150
HP:0002013HP:0002013Vomiting0NAA10 CL E G H826018704OMIM:300855Ogden syndrome23
HP:0002013HP:0002013Vomiting0NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiencyHP:0040282 - Frequent36
HP:0002013HP:0002013Vomiting0NAGS CL E G H16241717996OMIM:237310N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY.36
HP:0002013HP:0002013Vomiting0NARS2 CL E G H7973126274ORPHA:79134DEND syndromeHP:0040283 - Occasional34
HP:0002013HP:0002013Vomiting0NAXD CL E G H5573925576OMIM:618321Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2.
HP:0002013HP:0002013Vomiting0NBAS CL E G H5159415625OMIM:616483INFANTILE LIVER FAILURE SYNDROME 2; ILFS225
HP:0002013HP:0002013Vomiting0ND1 CL E G H45357455ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002013HP:0002013Vomiting0ND1 CL E G H45357455ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0ND1 CL E G H45357455ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0ND2 CL E G H45367456ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002013HP:0002013Vomiting0ND2 CL E G H45367456ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ND3 CL E G H45377458ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002013HP:0002013Vomiting0ND3 CL E G H45377458ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ND4 CL E G H45387459ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0ND4 CL E G H45387459ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ND5 CL E G H45407461ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0ND5 CL E G H45407461ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0ND6 CL E G H45417462ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0ND6 CL E G H45417462ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0NDUFA1 CL E G H46947683ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent7
HP:0002013HP:0002013Vomiting0NDUFA11 CL E G H12632820371ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent32
HP:0002013HP:0002013Vomiting0NDUFA6 CL E G H47007690ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent1
HP:0002013HP:0002013Vomiting0NDUFAF1 CL E G H5110318828ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent40
HP:0002013HP:0002013Vomiting0NDUFAF2 CL E G H9194228086ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent26
HP:0002013HP:0002013Vomiting0NDUFAF3 CL E G H2591529918ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent31
HP:0002013HP:0002013Vomiting0NDUFAF4 CL E G H2907821034ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent50
HP:0002013HP:0002013Vomiting0NDUFAF5 CL E G H7913315899ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent34
HP:0002013HP:0002013Vomiting0NDUFAF8 CL E G H28418433551ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002013HP:0002013Vomiting0NDUFB10 CL E G H47167696ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent
HP:0002013HP:0002013Vomiting0NDUFB11 CL E G H5453920372ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent3
HP:0002013HP:0002013Vomiting0NDUFB3 CL E G H47097698ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent9
HP:0002013HP:0002013Vomiting0NDUFB9 CL E G H47157704ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent16
HP:0002013HP:0002013Vomiting0NDUFS1 CL E G H47197707ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent81
HP:0002013HP:0002013Vomiting0NDUFS1 CL E G H47197707OMIM:618226Mitochondrial complex I deficiency, nuclear type 5.81
HP:0002013HP:0002013Vomiting0NDUFS2 CL E G H47207708ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent65
HP:0002013HP:0002013Vomiting0NDUFS3 CL E G H47227710ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent22
HP:0002013HP:0002013Vomiting0NDUFS4 CL E G H47247711ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent27
HP:0002013HP:0002013Vomiting0NDUFS4 CL E G H47247711OMIM:252010Mitochondrial complex I deficiency, nuclear type 127
HP:0002013HP:0002013Vomiting0NDUFS6 CL E G H47267713ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent21
HP:0002013HP:0002013Vomiting0NDUFS7 CL E G H3742917714ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent38
HP:0002013HP:0002013Vomiting0NDUFS8 CL E G H47287715ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent42
HP:0002013HP:0002013Vomiting0NDUFV1 CL E G H47237716ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent74
HP:0002013HP:0002013Vomiting0NDUFV1 CL E G H47237716OMIM:618225Mitochondrial complex I deficiency, nuclear type 4.74
HP:0002013HP:0002013Vomiting0NDUFV2 CL E G H47297717ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent27
HP:0002013HP:0002013Vomiting0NEUROG3 CL E G H5067413806OMIM:610370Diarrhea 4, malabsorptive, congenital.5
HP:0002013HP:0002013Vomiting0NEUROG3 CL E G H5067413806ORPHA:83620Enteric anendocrinosisHP:0040281 - Very frequent5
HP:0002013HP:0002013Vomiting0NEXMIF CL E G H34053329433OMIM:300912Mental retardation, X-linked 9852
HP:0002013HP:0002013Vomiting0NFIX CL E G H47847788ORPHA:44798019p13.3 microduplication syndrome40
HP:0002013HP:0002013Vomiting0NLRC4 CL E G H5848416412OMIM:616050AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC30
HP:0002013HP:0002013Vomiting0NNT CL E G H235307863ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent13
HP:0002013HP:0002013Vomiting0NODAL CL E G H48387865ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent45
HP:0002013HP:0002013Vomiting0NODAL CL E G H48387865ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional45
HP:0002013HP:0002013Vomiting0NODAL CL E G H48387865ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent45
HP:0002013HP:0002013Vomiting0NODAL CL E G H48387865ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent45
HP:0002013HP:0002013Vomiting0NOTCH2NLC CL E G H10099671753924OMIM:603472NEURONAL INTRANUCLEAR INCLUSION DISEASE
HP:0002013HP:0002013Vomiting0NR3C2 CL E G H43067979OMIM:177735Pseudohypoaldosteronism, type I, autosomal dominant.109
HP:0002013HP:0002013Vomiting0NSD1 CL E G H6432414234OMIM:117550Sotos syndrome 1544
HP:0002013HP:0002013Vomiting0NUBPL CL E G H8022420278ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent89
HP:0002013HP:0002013Vomiting0OPLAH CL E G H268738149OMIM:2600055-@oxoprolinase deficiency.5
HP:0002013HP:0002013Vomiting0OTC CL E G H50098512OMIM:311250Ornithine transcarbamylase deficiency, hyperammonemia due to.369
HP:0002013HP:0002013Vomiting0OXCT1 CL E G H50198527OMIM:245050Succinyl CoA:3-oxoacid CoA transferase deficiency.52
HP:0002013HP:0002013Vomiting0PCCA CL E G H50958653OMIM:606054Propionic acidemia.96
HP:0002013HP:0002013Vomiting0PCCB CL E G H50968654OMIM:606054Propionic acidemia.92
HP:0002013HP:0002013Vomiting0PDCD10 CL E G H112358761ORPHA:221061Familial cerebral cavernous malformation21
HP:0002013HP:0002013Vomiting0PDSS2 CL E G H5710723041ORPHA:255249Leigh syndrome with nephrotic syndrome54
HP:0002013HP:0002013Vomiting0PERCC1 CL E G H10537104552293ORPHA:92050Congenital tufting enteropathyHP:0040284 - Very rare
HP:0002013HP:0002013Vomiting0PGM1 CL E G H52368905OMIM:614921Congenital disorder of glycosylation, type It58
HP:0002013HP:0002013Vomiting0PHGDH CL E G H262278923ORPHA:793513-phosphoglycerate dehydrogenase deficiency, infantile/juvenile formHP:0040282 - Frequent37
HP:0002013HP:0002013Vomiting0PHKA2 CL E G H52568926ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiencyHP:0040284 - Very rare54
HP:0002013HP:0002013Vomiting0PHKB CL E G H52578927ORPHA:79240Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency101
HP:0002013HP:0002013Vomiting0PHKG2 CL E G H52618931ORPHA:264580Glycogen storage disease due to liver phosphorylase kinase deficiencyHP:0040284 - Very rare48
HP:0002013HP:0002013Vomiting0PIGY CL E G H8499228213OMIM:616809Hyperphosphatasia with mental retardation syndrome 62
HP:0002013HP:0002013Vomiting0PKHD1 CL E G H53149016ORPHA:53035Caroli diseaseHP:0040283 - Occasional563
HP:0002013HP:0002013Vomiting0PLCH1 CL E G H2300729185ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0PLEC CL E G H53399069ORPHA:158684Epidermolysis bullosa simplex with pyloric atresiaHP:0040282 - Frequent759
HP:0002013HP:0002013Vomiting0PMM2 CL E G H53739115OMIM:212065Congenital disorder of glycosylation, type Ia.150
HP:0002013HP:0002013Vomiting0PMM2 CL E G H53739115ORPHA:79318PMM2-CDGHP:0040282 - Frequent150
HP:0002013HP:0002013Vomiting0PNPLA8 CL E G H5064028900OMIM:251950Mitochondrial myopathy with lactic acidosis3
HP:0002013HP:0002013Vomiting0PNPT1 CL E G H8717823166OMIM:608703Spinocerebellar ataxia 25.60
HP:0002013HP:0002013Vomiting0PNPT1 CL E G H8717823166ORPHA:101111Spinocerebellar ataxia type 25HP:0040283 - Occasional60
HP:0002013HP:0002013Vomiting0POLG CL E G H54289179OMIM:603041Mitochondrial DNA depletion syndrome 1 (mngie type).464
HP:0002013HP:0002013Vomiting0POLG CL E G H54289179OMIM:203700Mitochondrial DNA depletion syndrome 4A (Alpers type).464
HP:0002013HP:0002013Vomiting0POLG CL E G H54289179ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent464
HP:0002013HP:0002013Vomiting0PPM1D CL E G H84939277OMIM:617450Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold.22
HP:0002013HP:0002013Vomiting0PPOX CL E G H54989280OMIM:176200Porphyria variegata.41
HP:0002013HP:0002013Vomiting0PSAP CL E G H56609498ORPHA:206436Infantile Krabbe diseaseHP:0040283 - Occasional81
HP:0002013HP:0002013Vomiting0PTCH1 CL E G H57279585ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent665
HP:0002013HP:0002013Vomiting0PTCH1 CL E G H57279585ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional665
HP:0002013HP:0002013Vomiting0PTCH1 CL E G H57279585ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent665
HP:0002013HP:0002013Vomiting0PTCH1 CL E G H57279585ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent665
HP:0002013HP:0002013Vomiting0PYCR2 CL E G H2992030262ORPHA:481152PYCR2-related microcephaly-progressive leukoencephalopathyHP:0040282 - Frequent11
HP:0002013HP:0002013Vomiting0RANBP2 CL E G H59039848ORPHA:88619Familial acute necrotizing encephalopathyHP:0040282 - Frequent57
HP:0002013HP:0002013Vomiting0RARS1 CL E G H59179870ORPHA:438114RARS-related autosomal recessive hypomyelinating leukodystrophyHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0RECQL4 CL E G H94019949ORPHA:221016Rothmund-Thomson syndrome type 2HP:0040283 - Occasional445
HP:0002013HP:0002013Vomiting0RELA CL E G H59709955ORPHA:251636EpendymomaHP:0040283 - Occasional1
HP:0002013HP:0002013Vomiting0RET CL E G H59799967OMIM:142623Hirschsprung disease, susceptibility to, 1.572
HP:0002013HP:0002013Vomiting0RRM2B CL E G H5048417296OMIM:612075Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)125
HP:0002013HP:0002013Vomiting0RRM2B CL E G H5048417296ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent125
HP:0002013HP:0002013Vomiting0RYR1 CL E G H626110483ORPHA:466650Exercise-induced malignant hyperthermiaHP:0040283 - Occasional1200
HP:0002013HP:0002013Vomiting0SAA1 CL E G H628810513ORPHA:85445AA amyloidosisHP:0040282 - Frequent2
HP:0002013HP:0002013Vomiting0SAR1B CL E G H5112810535ORPHA:71Chylomicron retention diseaseHP:0040282 - Frequent8
HP:0002013HP:0002013Vomiting0SAR1B CL E G H5112810535OMIM:246700Chylomicron retention disease.8
HP:0002013HP:0002013Vomiting0SCN2A CL E G H632610588OMIM:618924EPISODIC ATAXIA, TYPE 9; EA9427
HP:0002013HP:0002013Vomiting0SCNN1A CL E G H633710599ORPHA:171876Generalized pseudohypoaldosteronism type 1HP:0040282 - Frequent67
HP:0002013HP:0002013Vomiting0SCNN1A CL E G H633710599OMIM:264350Pseudohypoaldosteronism, type I, autosomal recessive.67
HP:0002013HP:0002013Vomiting0SCNN1B CL E G H633810600ORPHA:171876Generalized pseudohypoaldosteronism type 1HP:0040282 - Frequent61
HP:0002013HP:0002013Vomiting0SCNN1G CL E G H634010602ORPHA:171876Generalized pseudohypoaldosteronism type 1HP:0040282 - Frequent57
HP:0002013HP:0002013Vomiting0SERPING1 CL E G H7101228OMIM:106100Angioedema, hereditary, 1.64
HP:0002013HP:0002013Vomiting0SERPING1 CL E G H7101228ORPHA:100050Hereditary angioedema type 1HP:0040282 - Frequent64
HP:0002013HP:0002013Vomiting0SHANK3 CL E G H8535814294OMIM:606232Phelan-Mcdermid syndrome53
HP:0002013HP:0002013Vomiting0SHH CL E G H646910848ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent67
HP:0002013HP:0002013Vomiting0SHH CL E G H646910848ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional67
HP:0002013HP:0002013Vomiting0SHH CL E G H646910848ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent67
HP:0002013HP:0002013Vomiting0SHH CL E G H646910848ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent67
HP:0002013HP:0002013Vomiting0SI CL E G H647610856ORPHA:35122Congenital sucrase-isomaltase deficiencyHP:0040282 - Frequent98
HP:0002013HP:0002013Vomiting0SIX3 CL E G H649610889ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent32
HP:0002013HP:0002013Vomiting0SIX3 CL E G H649610889ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional32
HP:0002013HP:0002013Vomiting0SIX3 CL E G H649610889ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent32
HP:0002013HP:0002013Vomiting0SIX3 CL E G H649610889ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent32
HP:0002013HP:0002013Vomiting0SLC12A1 CL E G H655710910OMIM:601678Bartter syndrome, type 1, antenatal.75
HP:0002013HP:0002013Vomiting0SLC12A3 CL E G H655910912OMIM:263800Gitelman syndrome145
HP:0002013HP:0002013Vomiting0SLC19A3 CL E G H8070416266OMIM:607483Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)110
HP:0002013HP:0002013Vomiting0SLC1A3 CL E G H650710941ORPHA:2131Alternating hemiplegia of childhoodHP:0040282 - Frequent63
HP:0002013HP:0002013Vomiting0SLC1A3 CL E G H650710941OMIM:612656Episodic ataxia, type 6.63
HP:0002013HP:0002013Vomiting0SLC22A12 CL E G H11608517989ORPHA:94088Hereditary renal hypouricemiaHP:0040283 - Occasional56
HP:0002013HP:0002013Vomiting0SLC22A5 CL E G H658410969OMIM:212140Carnitine deficiency, systemic primary.207
HP:0002013HP:0002013Vomiting0SLC22A5 CL E G H658410969ORPHA:158Systemic primary carnitine deficiencyHP:0040281 - Very frequent207
HP:0002013HP:0002013Vomiting0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040283 - Occasional82
HP:0002013HP:0002013Vomiting0SLC25A15 CL E G H1016610985ORPHA:415Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome88
HP:0002013HP:0002013Vomiting0SLC25A15 CL E G H1016610985OMIM:238970Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome88
HP:0002013HP:0002013Vomiting0SLC2A9 CL E G H5660613446ORPHA:94088Hereditary renal hypouricemiaHP:0040283 - Occasional57
HP:0002013HP:0002013Vomiting0SLC37A4 CL E G H25424061OMIM:619525CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw; CDG2W110
HP:0002013HP:0002013Vomiting0SLC5A1 CL E G H652311036ORPHA:35710Glucose-galactose malabsorptionHP:0040283 - Occasional74
HP:0002013HP:0002013Vomiting0SLC5A6 CL E G H888411041OMIM:618973NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE; NERIB
HP:0002013HP:0002013Vomiting0SLC6A8 CL E G H653511055OMIM:300352Creatine deficiency syndrome, X-linked.122
HP:0002013HP:0002013Vomiting0SLC7A7 CL E G H905611065ORPHA:470Lysinuric protein intoleranceHP:0040282 - Frequent104
HP:0002013HP:0002013Vomiting0SLC7A7 CL E G H905611065OMIM:222700Lysinuric protein intolerance.104
HP:0002013HP:0002013Vomiting0SMC1A CL E G H824311111ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent135
HP:0002013HP:0002013Vomiting0SMPD1 CL E G H660911120OMIM:257200Niemann-Pick disease, type A.164
HP:0002013HP:0002013Vomiting0SPINK1 CL E G H669011244ORPHA:103918Tropical pancreatitis34
HP:0002013HP:0002013Vomiting0SPP1 CL E G H669611255ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0SPTBN1 CL E G H671111275OMIM:619475DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA
HP:0002013HP:0002013Vomiting0SSR4 CL E G H674811326ORPHA:370927SSR4-CDGHP:0040281 - Very frequent12
HP:0002013HP:0002013Vomiting0ST3GAL5 CL E G H886910872OMIM:609056Salt and pepper developmental regression syndrome.47
HP:0002013HP:0002013Vomiting0STAG2 CL E G H1073511355ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent1
HP:0002013HP:0002013Vomiting0STAG2 CL E G H1073511355ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent1
HP:0002013HP:0002013Vomiting0STAR CL E G H677011359ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent45
HP:0002013HP:0002013Vomiting0STAT4 CL E G H677511365ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional2
HP:0002013HP:0002013Vomiting0STIL CL E G H649110879ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent99
HP:0002013HP:0002013Vomiting0STIL CL E G H649110879ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional99
HP:0002013HP:0002013Vomiting0STIL CL E G H649110879ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent99
HP:0002013HP:0002013Vomiting0STIL CL E G H649110879ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent99
HP:0002013HP:0002013Vomiting0STK11 CL E G H679411389ORPHA:2869Peutz-Jeghers syndromeHP:0040283 - Occasional740
HP:0002013HP:0002013Vomiting0STX3 CL E G H680911438OMIM:619445DIARRHEA 12, WITH MICROVILLUS ATROPHY; DIAR121
HP:0002013HP:0002013Vomiting0SUCLG1 CL E G H880211449ORPHA:17Fatal infantile lactic acidosis with methylmalonic aciduriaHP:0040283 - Occasional60
HP:0002013HP:0002013Vomiting0SUGCT CL E G H7978316001OMIM:231690Glutaric aciduria III.8
HP:0002013HP:0002013Vomiting0SUOX CL E G H682111460OMIM:272300SULFOCYSTEINURIA40
HP:0002013HP:0002013Vomiting0SYK CL E G H685011491OMIM:619381IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION; IMD821
HP:0002013HP:0002013Vomiting0SYT1 CL E G H685711509ORPHA:522077Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndromeHP:0040282 - Frequent1
HP:0002013HP:0002013Vomiting0TCN2 CL E G H694811653OMIM:275350Transcobalamin II deficiency.57
HP:0002013HP:0002013Vomiting0TDGF1 CL E G H699711701ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent1
HP:0002013HP:0002013Vomiting0TDGF1 CL E G H699711701ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional1
HP:0002013HP:0002013Vomiting0TDGF1 CL E G H699711701ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent1
HP:0002013HP:0002013Vomiting0TDGF1 CL E G H699711701ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent1
HP:0002013HP:0002013Vomiting0TGIF1 CL E G H705011776ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent32
HP:0002013HP:0002013Vomiting0TGIF1 CL E G H705011776ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional32
HP:0002013HP:0002013Vomiting0TGIF1 CL E G H705011776ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent32
HP:0002013HP:0002013Vomiting0TGIF1 CL E G H705011776ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent32
HP:0002013HP:0002013Vomiting0TIMM22 CL E G H2992817317OMIM:618851COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43; COXPD43
HP:0002013HP:0002013Vomiting0TIMMDC1 CL E G H513001321ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent1
HP:0002013HP:0002013Vomiting0TMEM126B CL E G H5586330883ORPHA:2609Isolated complex I deficiencyHP:0040281 - Very frequent4
HP:0002013HP:0002013Vomiting0TNF CL E G H712411892OMIM:157300Migraine with or without aura, susceptibility to, 1.7
HP:0002013HP:0002013Vomiting0TNFRSF1A CL E G H713211916OMIM:142680Periodic fever, familial, autosomal dominant131
HP:0002013HP:0002013Vomiting0TNFRSF1A CL E G H713211916ORPHA:32960Tumor necrosis factor receptor 1 associated periodic syndromeHP:0040282 - Frequent131
HP:0002013HP:0002013Vomiting0TOM1 CL E G H1004311982OMIM:619510IMMUNODEFICIENCY 85 AND AUTOIMMUNITY; IMD85
HP:0002013HP:0002013Vomiting0TP53 CL E G H715711998OMIM:260500Papilloma of choroid plexus.911
HP:0002013HP:0002013Vomiting0TREH CL E G H1118112266ORPHA:103909Trehalase deficiency2
HP:0002013HP:0002013Vomiting0TRMU CL E G H5568725481OMIM:613070Liver failure, infantile, transient.101
HP:0002013HP:0002013Vomiting0TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNF CL E G H45587481ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNH CL E G H45647487ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNK CL E G H45667489ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNL1 CL E G H45677490ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNL1 CL E G H45677490ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNQ CL E G H45727495ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNS1 CL E G H45747497ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNS2 CL E G H45757498ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNV CL E G H45777500ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TRNW CL E G H45787501ORPHA:550MELASHP:0040282 - Frequent
HP:0002013HP:0002013Vomiting0TRNW CL E G H45787501ORPHA:255210Mitochondrial DNA-associated Leigh syndrome
HP:0002013HP:0002013Vomiting0TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
HP:0002013HP:0002013Vomiting0TXNRD2 CL E G H1058718155ORPHA:361Familial glucocorticoid deficiencyHP:0040282 - Frequent85
HP:0002013HP:0002013Vomiting0TYMP CL E G H18903148OMIM:603041Mitochondrial DNA depletion syndrome 1 (mngie type).138
HP:0002013HP:0002013Vomiting0TYMP CL E G H18903148ORPHA:298Mitochondrial neurogastrointestinal encephalomyopathyHP:0040281 - Very frequent138
HP:0002013HP:0002013Vomiting0UNC45A CL E G H5589830594OMIM:619377OSTEOOTOHEPATOENTERIC SYNDROME; OOHE
HP:0002013HP:0002013Vomiting0UQCC2 CL E G H8430021237OMIM:615824Mitochondrial complex III deficiency, nuclear type 77
HP:0002013HP:0002013Vomiting0UQCRC2 CL E G H738512586OMIM:615160Mitochondrial complex III deficiency, nuclear type 517
HP:0002013HP:0002013Vomiting0YARS1 CL E G H856512840OMIM:619418NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2; IMNEPD2
HP:0002013HP:0002013Vomiting0ZEB2 CL E G H983914881OMIM:235730Mowat-Wilson syndrome.362
HP:0002013HP:0002013Vomiting0ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutation362
HP:0002013HP:0002013Vomiting0ZEB2 CL E G H983914881ORPHA:261537Mowat-Wilson syndrome due to monosomy 2q22362
HP:0002013HP:0002013Vomiting0ZFTA CL E G H6599828449ORPHA:251636EpendymomaHP:0040283 - Occasional
HP:0002013HP:0002013Vomiting0ZIC2 CL E G H754612873ORPHA:93925Alobar holoprosencephalyHP:0040282 - Frequent34
HP:0002013HP:0002013Vomiting0ZIC2 CL E G H754612873ORPHA:93924Lobar holoprosencephalyHP:0040283 - Occasional34
HP:0002013HP:0002013Vomiting0ZIC2 CL E G H754612873ORPHA:93926Midline interhemispheric variant of holoprosencephalyHP:0040282 - Frequent34
HP:0002013HP:0002013Vomiting0ZIC2 CL E G H754612873ORPHA:220386Semilobar holoprosencephalyHP:0040282 - Frequent34
HP:0002013HP:0025089Feculent vomiting1 CL E G H
HP:0002013HP:0002572Episodic vomiting1ACADVL CL E G H3792OMIM:201475Very long-chain acyl-CoA dehydrogenase deficiency200
HP:0002013HP:0002587Projectile vomiting1AIMP1 CL E G H925510648OMIM:260600Leukodystrophy, hypomyelinating, 3.4
HP:0002013HP:0002572Episodic vomiting1ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiencyHP:0040283 - Occasional62
HP:0002013HP:0002572Episodic vomiting1ALG11 CL E G H44013832456ORPHA:280071ALG11-CDGHP:0040283 - Occasional41
HP:0002013HP:0002587Projectile vomiting1ANO1 CL E G H5510721625OMIM:620045
HP:0002013HP:0002572Episodic vomiting1ARG1 CL E G H383663OMIM:207800Argininemia31
HP:0002013HP:0002572Episodic vomiting1ATP6 CL E G H45087414ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1CCM2 CL E G H8360521708ORPHA:221061Familial cerebral cavernous malformationHP:0040283 - Occasional37
HP:0002013HP:0002572Episodic vomiting1CDC42BPB CL E G H95781738OMIM:619841
HP:0002013HP:0002572Episodic vomiting1CDK13 CL E G H86211733OMIM:617360Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder8
HP:0002013HP:0002572Episodic vomiting1CDK8 CL E G H10241779OMIM:618748INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA
HP:0002013HP:0002587Projectile vomiting1CLMP CL E G H7982724039OMIM:615237Congenital short bowel syndrome7
HP:0002013HP:0002572Episodic vomiting1COQ2 CL E G H2723525223OMIM:607426Coenzyme Q10 deficiency, primary, 154
HP:0002013HP:0002572Episodic vomiting1COQ2 CL E G H2723525223ORPHA:255249Leigh syndrome with nephrotic syndromeHP:0040282 - Frequent54
HP:0002013HP:0002572Episodic vomiting1COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyriaHP:0040282 - Frequent72
HP:0002013HP:0002572Episodic vomiting1CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1D2HGDH CL E G H72829428358OMIM:600721D-2-Hydroxyglutaric aciduria 1.102
HP:0002013HP:0002572Episodic vomiting1FAH CL E G H21843579OMIM:276700Tyrosinemia, type I107
HP:0002013HP:0002572Episodic vomiting1GAMT CL E G H25934136OMIM:612736Cerebral creatine deficiency syndrome 291
HP:0002013HP:0002572Episodic vomiting1GK CL E G H27104289OMIM:307030Glycerol kinase deficiency.13
HP:0002013HP:0002572Episodic vomiting1HMGCL CL E G H31555005ORPHA:203-hydroxy-3-methylglutaric aciduriaHP:0040282 - Frequent35
HP:0002013HP:0002572Episodic vomiting1HNRNPK CL E G H31905044ORPHA:352665Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletionHP:0040283 - Occasional8
HP:0002013HP:0002572Episodic vomiting1HNRNPK CL E G H31905044ORPHA:453504Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutationHP:0040283 - Occasional8
HP:0002013HP:0002572Episodic vomiting1HS3ST6 CL E G H6471114178OMIM:619367ANGIOEDEMA, HEREDITARY, 8; HAE8
HP:0002013HP:0002572Episodic vomiting1KRIT1 CL E G H8891573ORPHA:221061Familial cerebral cavernous malformationHP:0040283 - Occasional92
HP:0002013HP:0002572Episodic vomiting1LBX1 CL E G H1066016960OMIM:619483CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3; CCHS3
HP:0002013HP:0002572Episodic vomiting1NAXD CL E G H5573925576OMIM:618321Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 2
HP:0002013HP:0002572Episodic vomiting1ND1 CL E G H45357455ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1ND2 CL E G H45367456ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1ND3 CL E G H45377458ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1ND4 CL E G H45387459ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1ND5 CL E G H45407461ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1ND6 CL E G H45417462ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1NEXMIF CL E G H34053329433OMIM:300912Mental retardation, X-linked 9852
HP:0002013HP:0002572Episodic vomiting1NFIX CL E G H47847788ORPHA:44798019p13.3 microduplication syndromeHP:0040283 - Occasional40
HP:0002013HP:0002572Episodic vomiting1NLRC4 CL E G H5848416412OMIM:616050AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC30
HP:0002013HP:0002572Episodic vomiting1NOTCH2NLC CL E G H10099671753924OMIM:603472NEURONAL INTRANUCLEAR INCLUSION DISEASE
HP:0002013HP:0002572Episodic vomiting1NSD1 CL E G H6432414234OMIM:117550Sotos syndrome 1544
HP:0002013HP:0002572Episodic vomiting1PDCD10 CL E G H112358761ORPHA:221061Familial cerebral cavernous malformationHP:0040283 - Occasional21
HP:0002013HP:0002572Episodic vomiting1PDSS2 CL E G H5710723041ORPHA:255249Leigh syndrome with nephrotic syndromeHP:0040282 - Frequent54
HP:0002013HP:0002572Episodic vomiting1PNPLA8 CL E G H5064028900OMIM:251950Mitochondrial myopathy with lactic acidosis.3
HP:0002013HP:0002572Episodic vomiting1SHANK3 CL E G H8535814294OMIM:606232Phelan-Mcdermid syndrome53
HP:0002013HP:0002572Episodic vomiting1SLC25A15 CL E G H1016610985ORPHA:415Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeHP:0040282 - Frequent88
HP:0002013HP:0002572Episodic vomiting1SLC25A15 CL E G H1016610985OMIM:238970Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome.88
HP:0002013HP:0002572Episodic vomiting1SLC5A6 CL E G H888411041OMIM:618973NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE; NERIB
HP:0002013HP:0002572Episodic vomiting1SUOX CL E G H682111460OMIM:272300SULFOCYSTEINURIA40
HP:0002013HP:0002587Projectile vomiting1TIMM22 CL E G H2992817317OMIM:618851COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43; COXPD43
HP:0002013HP:0002572Episodic vomiting1TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNK CL E G H45667489ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNL1 CL E G H45677490ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNV CL E G H45777500ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1TRNW CL E G H45787501ORPHA:255210Mitochondrial DNA-associated Leigh syndromeHP:0040282 - Frequent
HP:0002013HP:0002572Episodic vomiting1TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002013HP:0002572Episodic vomiting1UNC45A CL E G H5589830594OMIM:619377OSTEOOTOHEPATOENTERIC SYNDROME; OOHE
HP:0002013HP:0002572Episodic vomiting1UQCRC2 CL E G H738512586OMIM:615160Mitochondrial complex III deficiency, nuclear type 517
HP:0002013HP:0002572Episodic vomiting1ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutationHP:0040283 - Occasional362
HP:0002013HP:0002572Episodic vomiting1ZEB2 CL E G H983914881ORPHA:261537Mowat-Wilson syndrome due to monosomy 2q22HP:0040283 - Occasional362


Genes (339) :AASS ABCC6 ABCC8 ACAD8 ACADM ACADVL ACAT1 ACSF3 ACTG2 ACY1 ADNP AIMP1 AIP ALAD ALDH18A1 ALDOB ALG11 ALG3 ALG8 ALG9 ALPL ALX4 AMN ANAPC1 ANO1 APC AQP2 ARG1 ASL ASPA ASS1 ASXL1 ASXL3 ATP1A2 ATP1A3 ATP6 ATP6V0A4 ATP7B ATRX AVP AVPR2 BCKDHA BCKDHB BOLA3 BRAF BSND BTD CACNA1A CARD8 CAV1 CCM2 CD46 CD55 CDC42BPB CDH23 CDK13 CDK8 CDKN1A CDKN1B CDKN2B CDKN2C CDON CFH CFI CLCNKA CLCNKB CLMP COA8 COL1A1 COL4A5 COL4A6 COL5A1 COL5A2 COQ2 COX1 COX2 COX3 CPOX CPS1 CPT2 CTNNB1 CTNS CTRC CUBN CYC1 CYP11A1 CYP11B2 CYP24A1 CYTB D2HGDH DBH DBT DGAT1 DGUOK DHCR7 DISP1 DLD DLL1 DOLK DYRK1A EDNRA EGFR ELN ELP1 ENPP1 EPCAM ERBB3 ESR1 ETFA ETFB ETFDH F12 FAH FARSB FBLN5 FBP1 FGF8 FGFR1 FLNA FOCAD FOXH1 FOXP3 FOXRED1 GALC GALE GALT GAMT GAN GAS1 GFAP GFM2 GHSR GK GLA GLI2 GRB10 HADH HELLPAR HFE HIBCH HLA-DQA1 HLA-DQB1 HLCS HMBS HMGCL HMGCS2 HNF4A HNRNPK HPRT1 HS3ST6 HSD3B2 IRAK1 ITGB4 IVD KARS1 KCNJ1 KCNJ11 KIT KMT2E KRIT1 KYNU LAMA3 LAMB3 LAMC2 LBX1 LIG3 LIPA LPL MARS1 MC2R MCCC1 MCCC2 MED12 MEFV MEN1 MET MLYCD MMAA MMAB MMUT MPI MPV17 MRAP MRPS7 MSX2 MTHFD1 MTRR MTTP MVK NAA10 NAGS NARS2 NAXD NBAS 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 NEUROG3 NEXMIF NFIX NLRC4 NNT NODAL NOTCH2NLC NR3C2 NSD1 NUBPL OPLAH OTC OXCT1 PCCA PCCB PDCD10 PDSS2 PERCC1 PGM1 PHGDH PHKA2 PHKB PHKG2 PIGY PKHD1 PLCH1 PLEC PMM2 PNPLA8 PNPT1 POLG PPM1D PPOX PSAP PTCH1 PYCR2 RANBP2 RARS1 RECQL4 RELA RET RRM2B RYR1 SAA1 SAR1B SCN2A SCNN1A SCNN1B SCNN1G SERPING1 SHANK3 SHH SI SIX3 SLC12A1 SLC12A3 SLC19A3 SLC1A3 SLC22A12 SLC22A5 SLC25A13 SLC25A15 SLC2A9 SLC37A4 SLC5A1 SLC5A6 SLC6A8 SLC7A7 SMC1A SMPD1 SPINK1 SPP1 SPTBN1 SSR4 ST3GAL5 STAG2 STAR STAT4 STIL STK11 STX3 SUCLG1 SUGCT SUOX SYK SYT1 TCN2 TDGF1 TGIF1 TIMM22 TIMMDC1 TMEM126B TNF TNFRSF1A TOM1 TP53 TREH TRMU TRNC TRNF TRNH TRNK TRNL1 TRNQ TRNS1 TRNS2 TRNV TRNW TXNRD2 TYMP UNC45A UQCC2 UQCRC2 YARS1 ZEB2 ZFTA ZIC2

Diseases (270) :ORPHA:2203 ORPHA:51608 ORPHA:79134 ORPHA:79159 OMIM:201450 ORPHA:42 ORPHA:26793 OMIM:201475 OMIM:203750 ORPHA:134 ORPHA:289504 OMIM:614265 OMIM:155310 ORPHA:137754 ORPHA:404448 OMIM:260600 ORPHA:2965 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 OMIM:620045 ORPHA:99818 OMIM:125800 OMIM:207800 OMIM:207900 ORPHA:314911 OMIM:215700 ORPHA:97297 OMIM:615485 ORPHA:2131 ORPHA:255210 OMIM:602722 OMIM:277900 OMIM:309580 ORPHA:30925 OMIM:304800 OMIM:248600 OMIM:614299 OMIM:115150 ORPHA:89938 OMIM:253260 ORPHA:71518 OMIM:619079 OMIM:606721 ORPHA:221061 ORPHA:244242 OMIM:226300 OMIM:619841 ORPHA:91347 OMIM:617360 OMIM:618748 ORPHA:652 ORPHA:93925 ORPHA:93924 ORPHA:93926 ORPHA:220386 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:33402 ORPHA:411629 ORPHA:411634 ORPHA:103918 OMIM:615453 ORPHA:168558 ORPHA:289548 OMIM:203400 ORPHA:556030 OMIM:143880 ORPHA:137675 OMIM:600721 ORPHA:230 OMIM:615863 OMIM:251880 OMIM:270400 ORPHA:2394 OMIM:610768 ORPHA:464311 OMIM:157300 OMIM:616069 OMIM:223900 ORPHA:92050 OMIM:243180 OMIM:231680 OMIM:610618 OMIM:276700 OMIM:613658 ORPHA:348 OMIM:300048 OMIM:619991 ORPHA:37042 ORPHA:2609 ORPHA:206436 OMIM:245200 OMIM:230350 ORPHA:79239 OMIM:230400 OMIM:612736 OMIM:256850 ORPHA:363717 ORPHA:565624 ORPHA:314811 OMIM:307030 OMIM:301500 ORPHA:96182 ORPHA:71212 OMIM:176200 ORPHA:88639 OMIM:212750 OMIM:253270 OMIM:176000 ORPHA:20 OMIM:246450 OMIM:605911 ORPHA:263455 ORPHA:352665 ORPHA:453504 OMIM:300322 OMIM:619367 ORPHA:90791 ORPHA:93552 ORPHA:158684 OMIM:243500 OMIM:619147 OMIM:241200 ORPHA:79455 OMIM:618512 OMIM:236800 ORPHA:79404 OMIM:619483 ORPHA:298 OMIM:278000 OMIM:238600 OMIM:615486 ORPHA:361 OMIM:210200 OMIM:210210 OMIM:301068 OMIM:249100 OMIM:248360 OMIM:251100 OMIM:251110 OMIM:251000 OMIM:602579 ORPHA:79319 OMIM:256810 OMIM:617872 OMIM:617780 ORPHA:2169 ORPHA:14 OMIM:260920 OMIM:610377 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 OMIM:603472 OMIM:177735 OMIM:117550 OMIM:260005 OMIM:311250 OMIM:245050 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:481152 ORPHA:88619 ORPHA:438114 ORPHA:221016 ORPHA:251636 OMIM:142623 OMIM:612075 ORPHA:466650 ORPHA:85445 ORPHA:71 OMIM:246700 OMIM:618924 ORPHA:171876 OMIM:264350 OMIM:106100 ORPHA:100050 OMIM:606232 ORPHA:35122 OMIM:601678 OMIM:263800 OMIM:607483 OMIM:612656 ORPHA:94088 OMIM:212140 ORPHA:158 ORPHA:247585 ORPHA:415 OMIM:238970 OMIM:619525 ORPHA:35710 OMIM:618973 OMIM:300352 ORPHA:470 OMIM:222700 OMIM:257200 OMIM:619475 ORPHA:370927 OMIM:609056 ORPHA:2869 OMIM:619445 ORPHA:17 OMIM:231690 OMIM:272300 OMIM:619381 ORPHA:522077 OMIM:275350 OMIM:618851 OMIM:142680 ORPHA:32960 OMIM:619510 OMIM:260500 ORPHA:103909 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.