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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
2 associated genes
No signs/symptoms info
Adult-onset distal myopathy due to VCP mutation
Sarcoidosis

VCP BTNL2
HLA-DRB1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Adult-onset distal myopathy due to VCP mutation
VCP
Sarcoidosis
BTNL2 HLA-DRB1



Adult-onset distal myopathy due to VCP mutation
Sarcoidosis

Synonym(s):
(no synonyms)

Synonym(s):
- Besnier-Boeck-Schaumann disease
- Boeck sarcoid
- Boeck's sarcoid

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare endocrine disease
- Rare eye disease
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D012507

No signs/symptoms info available.