Somnolence

Symptom Information:

Symptom ID: HPO:0001262
Synonyms:
Drowsy (finding) [Orphanet:43450]
Drowsiness, function (observable entity) [Orphanet:43450]
Sleepy (finding) [Orphanet:43450]
Drowsiness [HPO:0001262]
Drowsiness [Orphanet:43450]
Sleepy [Orphanet:43450]
Somnolence [Orphanet:43450]
Somnolence [OMIM:Somnolence]
Somnolence/hypersomnia/parasomnia [Orphanet:43450]
Sleepiness [Orphanet:43450]
Somnolence [MedDRA:10041349]
Daytime sleepiness [MedDRA:10041349]
Drowsiness [MedDRA:10041349]
Drowsy on awakening [MedDRA:10041349]
Excessive daytime sleepiness [MedDRA:10041349]
Feeling of residual sleepiness [MedDRA:10041349]
Groggy [MedDRA:10041349]
Groggy and sluggish [MedDRA:10041349]
Groggy on awakening [MedDRA:10041349]
Hard to awaken [MedDRA:10041349]
Less alert on arising [MedDRA:10041349]
Sleepiness [MedDRA:10041349]
Sleepy [MedDRA:10041349]
Parasomnia [MedDRA:10061910]
Parasomnia (disorder) [Orphanet:43450]
Parasomnias [Orphanet:43450]
Quality:
Cross references:
Orphanet:43450 "Somnolence/hypersomnia/parasomnia" [Orphanet:43450]
OMIM: "Somnolence" [OMIM:Somnolence]
UMLS:C0013144 "Drowsiness" [HPO:0001262]
UMLS:C0013144 "Drowsiness" [Orphanet:43450]
UMLS:C0234450 "Sleepy" [Orphanet:43450]
UMLS:C2830004 "Somnolence" [Orphanet:43450]
UMLS:C0030508 "Parasomnias" [Orphanet:43450]
Is a (Direct Parents):
HPO         Reduced consciousness/confusion
MedDRA Sleep disturbance
Orphanet Sleep disturbance
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)