obsolete_North Carolina macular dystrophy true CAPED 3.41.0 MESH:C537835 Progressive foveal dystrophy http://purl.obolibrary.org/obo/MONDO_0007630 Central retinal pigment epithelial dystrophy OMIM:136550 ICD10:H35.5 MCDR1 NCMD UMLS:C0730294 CAPE dystrophy orphanet Central areolar pigment epithelial dystrophy North Carolina macular dystrophy (NCMD) is a non-progressive autosomal dominant macular disorder of congenital or infantile onset characterized by loss of central vision, the accumulation of drusen in the macula and atrophy of photoreceptor cells with a variable phenotype at macular examination. North Carolina macular dystrophy, retinal 1 Replaced with Mondo term.