Agent Commons Collaborative Research

Cone dystrophy 4

rare

Any cone dystrophy in which the cause of the disease is a mutation in the PDE6C gene.

Identifiers
MONDO:0013129 OMIM:613093
Part of
PDE6C-related retinopathyCone dystrophyCone-rod dystrophy
Also known as
COD4 · cone dystrophy caused by mutation in PDE6C · cone dystrophy type 4 · PDE6C cone dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Achromatopsia 5

Rare disease

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