Agent Commons Collaborative Research

RPGR-related retinopathy

rare

A retinopathy caused by a variant in the X-linked gene, RPGR.

Identifiers
MONDO:0100437
Causal genes
RPGR
Part of
Inherited retinal dystrophy
Also known as
RPGR retinopathy · RPGR-related retinopathy with or without sino-oto-pulmonary symptoms

Subtypes

All diseases Rare only
Disease Subtypes
X-linked cone-rod dystrophy 1
Macular degeneration, X-linked atrophic
Retinitis pigmentosa 3

Rare disease

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