Nausea

Symptom Information:

Symptom ID: HPO:0002018
Synonyms:
Nausea (finding) [Orphanet:27180]
Nausea [Orphanet:27180]
Nausea [OMIM:Nausea]
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:0002017 "Nausea and vomiting" [Orphanet:27180]
Orphanet:27180 "Nausea/vomiting/regurgitation/merycism/hyperemesis" [Orphanet:27180]
OMIM: "Nausea" [OMIM:Nausea]
OMIM: "Nausea (in some patients)" [OMIM:Nausea (in some patients)]
UMLS:C1963179 "Nausea" [HPO:0002018]
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 Functional anomalies of the digestive system
Orphanet Vomiting
MedDRA Nausea and vomiting symptoms
HPO         Nausea and vomiting
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)
                Nausea(HPO:0002018)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Gastrointestinal signs and symptoms(MedDRA:10018012)
       Nausea and vomiting symptoms(MedDRA:10028817)
          Nausea(HPO:0002018)
Database Frequency: 44 / 7739
Resource:

All diseases associated with this symptom:

Acute intermittent porphyria (Orphanet:79276)
Alström syndrome (Orphanet:64)
Argininemia (Orphanet:90)
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM (OMIM:118301)
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE (OMIM:118230)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Classical phenylketonuria (Orphanet:79254)
Cystinosis (Orphanet:213)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
Episodic ataxia type 3 (Orphanet:79135)
Episodic ataxia type 4 (Orphanet:79136)
Fabry disease (Orphanet:324)
Familial lipoprotein lipase deficiency (Orphanet:309015)
Gaucher disease type 2 (Orphanet:77260)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA (OMIM:145590)
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO (OMIM:240150)
HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY (OMIM:241150)
Hereditary fructose intolerance (Orphanet:469)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hyperinsulinism-hyperammonemia syndrome (Orphanet:35878)
Hypouricemia, renal, 1 (OMIM:220150)
Hypouricemia, renal, 2 (OMIM:612076)
Idiopathic giant cell myocarditis (Orphanet:329874)
Lysinuric protein intolerance (Orphanet:470)
MELAS (Orphanet:550)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 (OMIM:157300)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10 (OMIM:610208)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11 (OMIM:610209)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3 (OMIM:607498)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5 (OMIM:607508)
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6 (OMIM:607516)
MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4 (OMIM:607501)
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 (OMIM:300125)
MONOSODIUM GLUTAMATE SENSITIVITY (OMIM:231630)
Menkes disease (Orphanet:565)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Nephronophthisis 2 (OMIM:602088)
Ovarian hyperstimulation syndrome (Orphanet:64739)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Peripartum cardiomyopathy (Orphanet:563)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)