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Cataract with Y-shaped suture opacities
4 OMIM references -
3 associated genes
15 connected diseases
No signs/symptoms info
Disease Type of connection
Zonular cataract
Nuclear cataract
Cerulean cataract
Total congenital cataract
Cataract-microcornea syndrome
Coppock-like cataract
Pulverulent cataract
Posterior polar cataract
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Catecholaminergic polymorphic ventricular tachycardia
Microphthalmia - 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:
4 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
CRYBA1 P05813123610
CRYBB2 P43320123620
MIP P30301154050
No signs/symptoms info available.