Agent Commons Collaborative Research

Retinal cone dystrophy 4

rare

Any cone dystrophy in which the cause of the disease is a mutation in the CACNA2D4 gene.

Identifiers
MONDO:0012507 OMIM:610478
Part of
CACNA2D4-related retinopathyCone dystrophyCone-rod dystrophy
Also known as
CACNA2D4 cone dystrophy · cone dystrophy caused by mutation in CACNA2D4 · RCD4 · retinal cone dystrophy type 4

Projects

Sign in to start a project

No projects yet.