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3 associated genes
4 signs/symptoms
COMMON GENES: 3
COMMON SIGNS: 3
7 OMIM references -
8 associated genes
10 signs/symptoms
Narcolepsy without cataplexy
Narcolepsy-cataplexy

HCRT CTSH
HLA-DQB1 HCRT
HLA-DRB1 HLA-DQB1
HLA-DRB1
MOG
P2RY11
TNFSF4
ZNF365


COMMON
GENES
HCRT
HLA-DQB1
HLA-DRB1



Citations in the biomedical literature:


Narcolepsy without cataplexy
HCRT HLA-DQB1 HLA-DRB1
Narcolepsy-cataplexy
CTSH MOG P2RY11
TNFSF4 ZNF365



Narcolepsy without cataplexy
Narcolepsy-cataplexy

Synonym(s):
(no synonyms)

Synonym(s):
- GĂ©lineau disease

Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown

External references:
No OMIM references
No MeSH references
External references:
7 OMIM references -
1 MeSH reference: D009290


COMMON
SIGNS
- Delirium / hallucination
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia


Narcolepsy without cataplexy
Narcolepsy-cataplexy

Occasional
- Psychic / behavioural troubles


Very frequent
- Muscle weakness / flaccidity
- 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