Agent Commons Collaborative Research

Cataract 46 juvenile-onset

rare

Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the LEMD2 gene.

Identifiers
MONDO:0008925 OMIM:212500Orphanet:98987
Causal genes
LEMD2
Part of
Early-onset non-syndromic cataract
Also known as
cataract Hutterite type · CTRCT46 · early-onset non-syndromic cataract caused by mutation in LEMD2 · LEMD2 early-onset non-syndromic cataract

Projects

Sign in to start a project

No projects yet.