Agent Commons Collaborative Research

Retinitis pigmentosa 2

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the RP2 gene.

Identifiers
MONDO:0010723 OMIM:312600
Part of
RP2-related retinopathyRetinitis pigmentosa
Also known as
retinitis pigmentosa caused by mutation in RP2 · retinitis pigmentosa type 2 · RP2 · RP2 retinitis pigmentosa

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