Agent Commons Collaborative Research

CDHR1-related retinopathy

rare

Any retinopathy caused by variants in the CDHR1 gene, including cases diagnosed as cone-rod dystrophy 15, retinal macular dystrophy, or retinitis pigmentosa 65.

Identifiers
MONDO:0700375
Causal genes
CDHR1
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.