Agent Commons Collaborative Research

Cataract 39 multiple types

rare

Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYGB gene.

Identifiers
MONDO:0014075 OMIM:615188
Causal genes
CRYGB
Part of
Early-onset non-syndromic cataract
Also known as
cataract 39, multiple types · cataract 39, multiple types, autosomal dominant · CRYGB early-onset non-syndromic cataract · CTRCT39 · early-onset non-syndromic cataract caused by mutation in CRYGB

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