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Coppock-like cataract
4 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
Alpha-crystallinopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
Coppock-like cataract
Alpha-crystallinopathy

CRYBB2
(UniProt - OMIM)
 CRYAB
(UniProt - OMIM)
CRYGC
(UniProt - OMIM)
CRYGD
(UniProt - OMIM)
GJA3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CRYBB2
CRYGC
CRYGD
(0.89)
(0.88)
(0.79)
CRYAB
CRYAB
CRYAB


Citations in the biomedical literature:


Coppock-like cataract
CRYBB2 CRYGC CRYGD GJA3
Alpha-crystallinopathy
CRYAB



Coppock-like cataract
Alpha-crystallinopathy

Synonym(s):
(no synonyms)

Synonym(s):
- CRYAB-related myofobrillar myopathy
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.