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3 associated genes
4 signs/symptoms
COMMON GENES: 1
1 associated gene
No signs/symptoms info
Narcolepsy without cataplexy
Limited systemic sclerosis

HCRT HLA-DRB1
HLA-DQB1
HLA-DRB1


COMMON
GENES
HLA-DRB1



Citations in the biomedical literature:


Narcolepsy without cataplexy
HCRT HLA-DQB1 HLA-DRB1
Limited systemic sclerosis



Narcolepsy without cataplexy
Limited systemic sclerosis

Synonym(s):
(no synonyms)

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: unknown
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:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

Narcolepsy without cataplexy

Very frequent
- Delirium / hallucination
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia

Occasional
- Psychic / behavioural troubles


Limited systemic sclerosis

(no data available)