inherited retinal dystrophy retinitis pigmentosa DOID:10584 GARD:0005694 ICD10:H35.5 ICD10:H35.52 MESH:D012174 MONDO:0019200 MedDRA:10038914 NCIT:C85045 OMIM:268000 OMIMPS:268000 Orphanet:791 Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades. Rod-cone dystrophy SCTID:28835009 UMLS:C0035334 UMLS:C4072872 pericentral pigmentary retinopathy