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Coralliform cataract
2 OMIM references -
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Zonular cataract
Cataract-microcornea syndrome
Nuclear cataract
Coppock-like cataract
Cerulean cataract
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Pulverulent cataract
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
CRYGD P07320123690
No signs/symptoms info available.