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Adult-onset distal myopathy due to VCP mutation
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal amyloidosis due to Apolipoprotein AI variant
1 associated gene
No signs/symptoms info
Adult-onset distal myopathy due to VCP mutation
Familial renal amyloidosis due to Apolipoprotein AI variant

VCP
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VCP
(0.63)
APOA1


Citations in the biomedical literature:


Adult-onset distal myopathy due to VCP mutation
VCP
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



Adult-onset distal myopathy due to VCP mutation
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
(no synonyms)

Synonym(s):
- Apolipoprotein AI amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AI variant
- Hereditary amyloid nephropathy due to apolipoprotein AI variant
- Hereditary renal amyloidosis due to apolipoprotein AI variant
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.