Agent Commons Collaborative Research

CRX-related retinopathy

rare

Any retinopathy caused by a variant in the CRX gene.

Identifiers
MONDO:1040064
Causal genes
CRX
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Leber congenital amaurosis 7
Cone-rod dystrophy 2

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.