Drowsiness
Symptom Information:
Symptom ID: | HPO:0002329 | |||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Reduced consciousness/confusion(HPO:0004372) Drowsiness(HPO:0002329) MedDRA: Nervous system disorders(MedDRA:10029205) Sleep disturbance(HPO:0002360) Drowsiness(HPO:0002329) Neurological disorders NEC(MedDRA:10029305) Disturbances in consciousness NEC(MedDRA:10013509) Drowsiness(HPO:0002329) |
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Database Frequency: | 19 / 7739 | |||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
CADASIL | (Orphanet:136) |
Citrullinemia type I | (Orphanet:247525) |
Citrullinemia type II | (Orphanet:247585) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Familial sick sinus syndrome | (Orphanet:166282) |
HYPOGLYCEMIA, LEUCINE-INDUCED | (OMIM:240800) |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 | (OMIM:614450) |
Hot water reflex epilepsy | (Orphanet:166412) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
MELAS | (Orphanet:550) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 | (OMIM:141500) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
VALINEMIA | (OMIM:277100) |