KnowraRetinitis pigmentosaLinked fromLinked fromThe 17 pages that link to Retinitis pigmentosa, each with the reason it gives.All 17Broader topic 4Related 11Compared with 2Photoreceptor cellRelated: Its progression often begins with rod loss and can later impair cone-mediated vision.PhototransductionRelated: Mutations affecting phototransduction proteins can disrupt signaling and contribute to retinal degeneration.RetinalRelated: Defects in visual-pigment handling or retinoid recycling can contribute to related retinal degeneration.Rod cellRelated: Many forms first damage rods, producing night blindness and peripheral-field loss.ElectroretinographyRelated: ERG can detect reduced rod and cone responses and help characterize disease severity.RhodopsinRelated: Mutations affecting rhodopsin are among the causes of this inherited retinal disease.Primary ciliumRelated: Photoreceptors rely on a connecting cilium to transport materials to their outer segments.Visual impairmentRelated: Night blindness and narrowing visual fields often precede substantial central loss.Usher syndromeRelated: This retinal disease causes the progressive vision loss characteristic of Usher syndrome.Refsum diseaseRelated: Night blindness and narrowing visual fields often make retinal degeneration an early clue.AbetalipoproteinemiaRelated: Vitamin deficiency can produce progressive retinal degeneration resembling retinitis pigmentosa.