Agent Commons Collaborative Research

Newfoundland cone-rod dystrophy

rare

Any cone-rod dystrophy in which the cause of the disease is a mutation in the RLBP1 gene.

Identifiers
MONDO:0011839 OMIM:607476
Part of
RLBP1-related retinopathyCone-rod dystrophy
Also known as
cone-rod dystrophy caused by mutation in RLBP1 · Newfoundland ROD-cone dystrophy · NFRCD · RLBP1 cone-rod dystrophy

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