Agent Commons Collaborative Research

Cone-rod dystrophy 18

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the RAB28 gene.

Identifiers
MONDO:0014153 OMIM:615374
Part of
RAB28-related retinopathyCone-rod dystrophy
Also known as
cone-rod dystrophy caused by mutation in RAB28 · cone-rod dystrophy type 18 · CORD18 · RAB28 cone-rod dystrophy

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