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Narcolepsy-cataplexy
7 OMIM references -
8 associated genes
10 signs/symptoms
COMMON GENES: 1
Limited systemic sclerosis
1 associated gene
No signs/symptoms info
Narcolepsy-cataplexy
Limited systemic sclerosis

CTSH
(UniProt - OMIM)
 HLA-DRB1
(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)

COMMON
GENES 		HLA-DRB1


Citations in the biomedical literature:


Narcolepsy-cataplexy
CTSH HCRT HLA-DQB1 HLA-DRB1 MOG P2RY11
TNFSF4 ZNF365
Limited systemic sclerosis



Narcolepsy-cataplexy
Limited systemic sclerosis

Synonym(s):
- Gélineau disease
Synonym(s):
- Systemic sclerosis sine scleroderma
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare renal disease
- Rare respiratory disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
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: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
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


Limited systemic sclerosis

(no data available)