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

HLA-DRB1
(UniProt - OMIM)
 HCRT
(UniProt - OMIM)
HLA-DQB1
(UniProt - OMIM)
HLA-DRB1
(UniProt - OMIM)

COMMON
GENES 		HLA-DRB1


Citations in the biomedical literature:


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



Limited systemic sclerosis
Narcolepsy without cataplexy

Synonym(s):
- Systemic sclerosis sine scleroderma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare renal disease
- Rare respiratory disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown
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)