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Narcolepsy-cataplexy
7 OMIM references -
8 associated genes
10 signs/symptoms
PROTEIN INTERACTIONS: 1
Adult-onset distal myopathy due to VCP mutation
1 associated gene
No signs/symptoms info
Narcolepsy-cataplexy
Adult-onset distal myopathy due to VCP mutation

CTSH
(UniProt - OMIM)
 VCP
(UniProt - OMIM)
HCRT
(UniProt - OMIM)
HLA-DQB1
(UniProt - OMIM)
HLA-DRB1
(UniProt - OMIM)
MOG
(UniProt - OMIM)
P2RY11
(UniProt - OMIM)
TNFSF4
(UniProt - OMIM)
ZNF365
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HLA-DRB1
(0.63)
VCP


Citations in the biomedical literature:


Narcolepsy-cataplexy
CTSH HCRT HLA-DQB1 HLA-DRB1 MOG P2RY11
TNFSF4 ZNF365
Adult-onset distal myopathy due to VCP mutation
VCP



Narcolepsy-cataplexy
Adult-onset distal myopathy due to VCP mutation

Synonym(s):
- Gélineau disease
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
7 OMIM references -
1 MeSH reference: D009290
External references:
No OMIM references
No MeSH references
Narcolepsy-cataplexy

Very frequent
- Delirium / hallucination
- Muscle weakness / flaccidity
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia
- Troubles of memory / amnesia / hypermnesia

Frequent
- Abnormal eye movements / oculomotor disorder
- Anomalies of eyes and vision

Occasional
- Collapse / sudden death / cardiac arrest / cardiorespiratory arrest
- Generalized obesity
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia


Adult-onset distal myopathy due to VCP mutation

(no data available)