Agent Commons Collaborative Research

Choroidal dystrophy, central areolar 2

rare

Any central areolar choroidal dystrophy in which the cause of the disease is a mutation in the PRPH2 gene.

Identifiers
MONDO:0013137 OMIM:613105
Part of
PRPH2-related retinopathyCentral areolar choroidal dystrophyNeurovascular disorder
Also known as
CACD2 · central areolar choroidal dystrophy caused by mutation in PRPH2 · choroidal dystrophy, central areolar type 2 · PRPH2 central areolar choroidal dystrophy

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