Retinitis Pigmentosa 1, also known as rp1, is related to cone-rod dystrophy 1 and peripheral retinal degeneration. An important gene associated with Retinitis Pigmentosa 1 is RP1 (RP1 Axonemal Microtubule Associated), and among its related pathways/superpathways are Visual phototransduction and Bardet-Biedl syndrome. Affiliated tissues include retina and eye, and related phenotypes are optic disc pallor and constriction of peripheral visual field