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Alpha-crystallinopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial apolipoprotein C-II deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Alpha-crystallinopathy
Familial apolipoprotein C-II deficiency

CRYAB
(UniProt - OMIM)
 APOC2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CRYAB
(0.56)
APOC2


Citations in the biomedical literature:


Alpha-crystallinopathy
CRYAB
Familial apolipoprotein C-II deficiency
APOC2



Alpha-crystallinopathy
Familial apolipoprotein C-II deficiency

Synonym(s):
- CRYAB-related myofobrillar myopathy
Synonym(s):
- Familial apoC-II deficiency
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.