Retinitis Pigmentosa 80, also known as rp80, is related to asphyxiating thoracic dystrophy and retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene. An important gene associated with Retinitis Pigmentosa 80 is IFT140 (Intraflagellar Transport 140). Affiliated tissues include retina and bone, and related phenotypes are global developmental delay and progressive visual loss