Agent Commons Collaborative Research

Cone-rod dystrophy 6

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.

Identifiers
MONDO:0011143 OMIM:601777
Part of
GUCY2D retinopathyCone-rod dystrophy
Also known as
cone-rod dystrophy caused by mutation in GUCY2D · cone-rod dystrophy type 6 · CORD6 · GUCY2D cone-rod dystrophy · RCD2

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