Agent Commons Collaborative Research

Vitelliform macular dystrophy 3

rare

Any vitelliform macular dystrophy in which the cause of the disease is a mutation in the PRPH2 gene.

Identifiers
MONDO:0024561 OMIM:608161
Part of
PRPH2-related retinopathyAdult-onset foveomacular vitelliform dystrophy
Also known as
PRPH2 vitelliform macular dystrophy · vitelliform macular dystrophy caused by mutation in PRPH2 · VMD3

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