RPGR retinopathy
RPGR-related retinopathy with or without sino-oto-pulmonary symptoms
COD1
CORDX1
RP3
RPGR retinitis pigmentosa
X-linked cone dystrophy 1
X-linked cone-rod dystrophy 1
X-linked cone-rod dystrophy type 1
choroidoretinal degeneration with retinal reflex in heterozygous women
cone dystrophy 1, X-linked
cone dystrophy X-linked 1
cone-rod degeneration, X-linked
cone-rod dystrophy X-linked 1
cone-rod dystrophy, X-linked, 1
cone-rod dystrophy, X-linked, type 1
macular degeneration, X-linked atrophic
retinal ciliopathy due to mutation in the RPGR gene
retinitis pigmentosa 15
retinitis pigmentosa 3
retinitis pigmentosa caused by mutation in RPGR
retinitis pigmentosa type 3