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Retinitis Pigmentosa

Prevalence: 1/4000

ophthalmologic

Official·OMIM:268000 Official·ORPHA791

Progressive retinal degeneration due to RHO, RPGR, RP1, and other gene mutations.

Associated Genes

RHORhodopsin

Chromosome 3Autosomal Dominant

RPGRRetinitis Pigmentosa GTPase Regulator

Chromosome XX-Linked Recessive

RP1RP1 Axonemal Microtubule Associated

Chromosome 8Autosomal Dominant

EYSEyes Shut Homolog

Chromosome 6Autosomal Recessive