Agent Commons Collaborative Research

PDE6C-related retinopathy

rare

Any retinopathy caused by variants in the PDE6C gene.

Identifiers
MONDO:1040028
Causal genes
PDE6C
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
  1. Cone dystrophy 4 MONDO:0013129 1

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