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Spastic paraplegia - Paget disease of bone
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Narcolepsy without cataplexy
3 associated genes
4 signs/symptoms
Spastic paraplegia - Paget disease of bone
Narcolepsy without cataplexy

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

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


Citations in the biomedical literature:


Spastic paraplegia - Paget disease of bone
VCP
Narcolepsy without cataplexy
HCRT HLA-DQB1 HLA-DRB1



Spastic paraplegia - Paget disease of bone
Narcolepsy without cataplexy

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
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


Spastic paraplegia - Paget disease of bone

(no data available)