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Adult-onset distal myopathy due to VCP mutation
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
1 OMIM reference -
1 associated gene
No signs/symptoms info
Adult-onset distal myopathy due to VCP mutation
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E

VCP
(UniProt - OMIM)
 INF2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VCP
(0.63)
INF2


Citations in the biomedical literature:


Adult-onset distal myopathy due to VCP mutation
VCP
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
INF2



Adult-onset distal myopathy due to VCP mutation
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E

Synonym(s):
(no synonyms)

Synonym(s):
- CMTDIE
- Charcot-Marie-Tooth disease - nephropathy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the genitourinary 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: <1 / 1 000 000
Average age onset: no data available
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.