Hypersomnia

Symptom Information:

Symptom ID: HPO:0100786
Synonyms:
Hypersomnia (disorder) [Orphanet:43450]
Hypersomnia [Orphanet:43450]
Somnolence/hypersomnia/parasomnia [Orphanet:43450]
Hypersomnia [MedDRA:10020765]
Other hypersomnia [MedDRA:10020765]
Persistent disorder of initiating or maintaining wakefulness [MedDRA:10020765]
Primary hypersomnia [MedDRA:10020765]
Sleep excessive [MedDRA:10020765]
Transient disorder of initiating or maintaining wakefulness [MedDRA:10020765]
Parasomnia [MedDRA:10061910]
Parasomnia (disorder) [Orphanet:43450]
Parasomnias [Orphanet:43450]
Quality:
Cross references:
Orphanet:43450 "Somnolence/hypersomnia/parasomnia" [Orphanet:43450]
UMLS:C0917799 "Hypersomnia" [HPO:0100786]
UMLS:C0917799 "Hypersomnia" [Orphanet:43450]
UMLS:C0030508 "Parasomnias" [Orphanet:43450]
Is a (Direct Parents):
Orphanet Somnolence
Orphanet Sleep disturbance
MedDRA Narcolepsy and hypersomnia
HPO         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)
                Behavioral abnormality(HPO:0000708)
                   Sleep disturbance(HPO:0002360)
                      Hypersomnia(HPO:0100786)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Sleep disturbance(HPO:0002360)
       Narcolepsy and hypersomnia(MedDRA:10028714)
          Hypersomnia(HPO:0100786)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Myopathy due to myoadenylate deaminase deficiency (OMIM:615511)
Steinert myotonic dystrophy (Orphanet:273)
Wolfram syndrome 1 (OMIM:222300)