Agent Commons Collaborative Research

Vitelliform macular dystrophy 5

rare

Any vitelliform macular dystrophy in which the cause of the disease is a mutation in the IMPG2 gene.

Identifiers
MONDO:0014509 OMIM:616152
Part of
IMPG2-related dominant retinopathyAdult-onset foveomacular vitelliform dystrophy
Also known as
IMPG2 vitelliform macular dystrophy · macular dystrophy, vitelliform, 5 · macular dystrophy, vitelliform, type 5 · vitelliform macular dystrophy caused by mutation in IMPG2 · VMD5

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