Nausea and vomiting
Symptom Information:
Symptom ID: | HPO:0002017 | |||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abdominal symptom(HPO:0011458) Nausea and vomiting(HPO:0002017) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal signs and symptoms(MedDRA:10018012) Nausea and vomiting symptoms(MedDRA:10028817) Nausea and vomiting(HPO:0002017) |
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Database Frequency: | 134 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acute intermittent porphyria | (Orphanet:79276) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alexander disease | (Orphanet:58) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alport syndrome | (Orphanet:63) |
Alveolar echinococcosis | (Orphanet:284) |
Anisakiasis | (Orphanet:1070) |
Atypical teratoid tumor | (Orphanet:99966) |
Babesiosis | (Orphanet:108) |
Behçet disease | (Orphanet:117) |
Benign familial infantile seizures | (Orphanet:306) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
Botulism | (Orphanet:1267) |
CINCA syndrome | (Orphanet:1451) |
CREST syndrome | (Orphanet:90290) |
Carcinoma of the gallbladder | (Orphanet:56044) |
Carney triad | (Orphanet:139411) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Central diabetes insipidus | (Orphanet:178029) |
Cholera | (Orphanet:173) |
Cholestasis - lymphedema | (Orphanet:1414) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Choreoacanthocytosis | (Orphanet:2388) |
Classical phenylketonuria | (Orphanet:79254) |
Cogan syndrome | (Orphanet:1467) |
Cold agglutinin disease | (Orphanet:56425) |
Congenital sucrase-isomaltase deficiency | (Orphanet:35122) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Cutaneous mastocytosis | (Orphanet:66646) |
Cystinosis | (Orphanet:213) |
Cystinuria | (Orphanet:214) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Dengue fever | (Orphanet:99828) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Dracunculiasis | (Orphanet:231) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Encephalopathy due to sulfite oxidase deficiency | (Orphanet:833) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Erdheim-Chester disease | (Orphanet:35687) |
Esophageal adenocarcinoma | (Orphanet:99976) |
Esophageal squamous cell carcinoma | (Orphanet:99977) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Familial cold urticaria | (Orphanet:47045) |
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Foodborne botulism | (Orphanet:228371) |
Galactose epimerase deficiency | (Orphanet:79238) |
Galactosemia | (Orphanet:352) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Griscelli disease type 2 | (Orphanet:79477) |
Hall-Riggs syndrome | (Orphanet:2107) |
Hereditary central diabetes insipidus | (Orphanet:30925) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary folate malabsorption | (Orphanet:90045) |
Hereditary fructose intolerance | (Orphanet:469) |
Hereditary nonpolyposis colon cancer | (Orphanet:144) |
Hirschsprung disease | (Orphanet:388) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Homocystinuria without methylmalonic aciduria | (Orphanet:622) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hydatidiform mole | (Orphanet:99927) |
Hydatidosis | (Orphanet:400) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Inhalational botulism | (Orphanet:254504) |
Intestinal botulism | (Orphanet:178481) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Kawasaki disease | (Orphanet:2331) |
L1 syndrome | (Orphanet:275543) |
Lassa fever | (Orphanet:99824) |
Legionellosis | (Orphanet:549) |
Leigh syndrome | (Orphanet:506) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Lujo hemorrhagic fever | (Orphanet:319213) |
Lyell syndrome | (Orphanet:537) |
Lyme disease | (Orphanet:91546) |
MELAS | (Orphanet:550) |
Maculopapular cutaneous mastocytosis | (Orphanet:79457) |
Malignant atrophic papulosis | (Orphanet:679) |
Marburg hemorrhagic fever | (Orphanet:99826) |
Marshall syndrome with periodic fever | (Orphanet:42642) |
Mastocytosis | (Orphanet:98292) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Menetrier disease | (Orphanet:2494) |
Menkes disease | (Orphanet:565) |
Methylmalonic acidemia without homocystinuria | (Orphanet:293355) |
Microscopic polyangiitis | (Orphanet:727) |
Mixed connective tissue disease | (Orphanet:809) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Multiple carboxylase deficiency | (Orphanet:148) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Nodular non-suppurative panniculitis | (Orphanet:33577) |
Non-histaminic angioedema | (Orphanet:658) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Palmoplantar keratoderma-esophageal carcinoma syndrome | (Orphanet:2198) |
Paroxysmal cold hemoglobinuria | (Orphanet:90035) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Porphyria | (Orphanet:738) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Primary peritoneal carcinoma | (Orphanet:168829) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Pseudohypoaldosteronism type 2 | (Orphanet:757) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Rabies | (Orphanet:770) |
Rhabdoid tumor | (Orphanet:69077) |
Rheumatic fever | (Orphanet:3099) |
Rift valley fever | (Orphanet:319251) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Rothmund-Thomson syndrome type 2 | (Orphanet:221016) |
Scleroderma | (Orphanet:801) |
Scrub typhus | (Orphanet:83317) |
Spontaneous periodic hypothermia | (Orphanet:29822) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Systemic mastocytosis | (Orphanet:2467) |
TRAPS syndrome | (Orphanet:32960) |
Viral hemorrhagic fever | (Orphanet:341) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
Von Hippel-Lindau disease | (Orphanet:892) |
Williams syndrome | (Orphanet:904) |
Wolman disease | (Orphanet:75233) |
Wyburn-Mason syndrome | (Orphanet:53719) |
Yellow fever | (Orphanet:99829) |