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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 3
4 OMIM references -
3 associated genes
No signs/symptoms info
Alpha-crystallinopathy
Cataract with Y-shaped suture opacities

CRYAB CRYBA1
CRYBB2
MIP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CRYAB
CRYAB
CRYAB
(0.89)
(0.89)
(0.65)
CRYBA1
CRYBB2
MIP



Citations in the biomedical literature:


Alpha-crystallinopathy
CRYAB
Cataract with Y-shaped suture opacities
CRYBA1 CRYBB2 MIP



Alpha-crystallinopathy
Cataract with Y-shaped suture opacities

Synonym(s):
- CRYAB-related myofobrillar myopathy

Synonym(s):
(no synonyms)

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.