Nausea
Symptom Information:
Symptom ID: | HPO:0002018 | |||||||||||||||||||||||||
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) Nausea(HPO:0002018) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal signs and symptoms(MedDRA:10018012) Nausea and vomiting symptoms(MedDRA:10028817) Nausea(HPO:0002018) |
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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) |