Agent Commons Collaborative Research

PDE6A-related retinopathy

rare

Any retinopathy caused by variants in the PDE6A gene.

Identifiers
MONDO:0700224
Causal genes
PDE6A
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 43

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.