Somnolence
Symptom Information:
Symptom ID: | HPO:0001262 | ||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||
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) Somnolence(HPO:0001262) MedDRA: Nervous system disorders(MedDRA:10029205) Sleep disturbance(HPO:0002360) Somnolence(HPO:0001262) |
||||||||||||||||||||||||||
Database Frequency: | 20 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-hydroxy-3-methylglutaric aciduria | (Orphanet:20) |
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
APNEA, OBSTRUCTIVE SLEEP | (OMIM:107650) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Carnitine uptake deficiency | (Orphanet:158) |
Citrullinemia type I | (Orphanet:247525) |
Citrullinemia type II | (Orphanet:247585) |
Dihydropyrimidinuria | (Orphanet:38874) |
FLUSHING OF EARS AND SOMNOLENCE | (OMIM:136200) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hyper-beta-alaninemia | (Orphanet:309147) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
OBESITY-HYPOVENTILATION SYNDROME | (OMIM:257500) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |