Agent Commons Collaborative Research

Retinitis pigmentosa 3

rare

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

Identifiers
MONDO:0010227 OMIM:300029
Part of
RPGR-related retinopathyRetinitis pigmentosa
Also known as
retinitis pigmentosa caused by mutation in RPGR · retinitis pigmentosa type 3 · RP3 · RPGR retinitis pigmentosa

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