Nausea and vomiting

Symptom Information:

Symptom ID: HPO:0002017
Synonyms:
Nausea [Orphanet:27180]
Nausea (finding) [Orphanet:27180]
Nausea and vomiting [OMIM:Nausea and vomiting]
Nausea/vomiting/regurgitation/merycism/hyperemesis [Orphanet:27180]
Nausea [MedDRA:10028813]
Churning of stomach [MedDRA:10028813]
Feeling queasy [MedDRA:10028813]
Nausea alone [MedDRA:10028813]
Nauseated [MedDRA:10028813]
Nauseous [MedDRA:10028813]
Queasy [MedDRA:10028813]
Sickness/nausea [MedDRA:10028813]
Nausea aggravated [MedDRA:10028813]
Nausea post chemotherapy [MedDRA:10028813]
Postprandial nausea [MedDRA:10028813]
Nausea post radiotherapy [MedDRA:10028813]
Nausea (in some patients) [OMIM:Nausea (in some patients)]
Merycism [MedDRA:10027387]
Rumination (finding) [Orphanet:27180]
Rumination [Orphanet:27180]
Regurgitation [MedDRA:10067171]
Regurgitation (finding) [Orphanet:27180]
Regurgitates after swallowing (finding) [Orphanet:27180]
Regurgitation [Orphanet:27180]
Regurgitates after swallowing [Orphanet:27180]
Quality:
Cross references:
HPO:0002018 "Nausea" [Orphanet:27180]
Orphanet:27180 "Nausea/vomiting/regurgitation/merycism/hyperemesis" [Orphanet:27180]
OMIM: "Nausea and vomiting" [OMIM:Nausea and vomiting]
OMIM: "Nausea (in some patients)" [OMIM:Nausea (in some patients)]
UMLS:C0027497 "Nausea" [Orphanet:27180]
UMLS:C0232604 "Rumination" [Orphanet:27180]
UMLS:C2004489 "Regurgitation" [Orphanet:27180]
UMLS:C0232605 "Regurgitates after swallowing" [Orphanet:27180]
Is a (Direct Parents):
Orphanet Vomiting
Orphanet Functional anomalies of the digestive system
MedDRA Nausea and vomiting symptoms
HPO         Abdominal symptom
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)
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)