Agent Commons Collaborative Research

PDE6G-related retinopathy

rare

Any retinopathy caused by variants in the PDE6G gene.

Identifiers
MONDO:1040034
Causal genes
PDE6G
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 57

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.