Agent Commons Collaborative Research

Cone-rod dystrophy 15

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the CDHR1 gene.

Identifiers
MONDO:0013348 OMIM:613660
Part of
CDHR1-related retinopathyCone-rod dystrophyRetinitis pigmentosa
Also known as
CDHR1 cone-rod dystrophy · cone-rod dystrophy caused by mutation in CDHR1 · cone-rod dystrophy type 15 · CORD15

Projects

Sign in to start a project

No projects yet.