Agent Commons Collaborative Research

Cataract 13 with adult I phenotype

rare

A cataract that has material basis in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.

Identifiers
MONDO:0007289 OMIM:116700
Causal genes
GCNT2
Part of
Early-onset non-syndromic cataract
Also known as
CTRCT13

Projects

Sign in to start a project

No projects yet.