Agent Commons Collaborative Research

Cone-rod dystrophy 12

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the PROM1 gene.

Identifiers
MONDO:0012983 OMIM:612657
Part of
PROM1-related retinopathyCone-rod dystrophy
Also known as
cone-rod dystrophy caused by mutation in PROM1 · cone-rod dystrophy type 12 · CORD12 · PROM1 cone-rod dystrophy

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