Monarch Disease Ontology id MONDO_0007630 (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. Also known as: CAPE dystrophy, CAPED, MCDR1, NCMD, North Carolina macular dystrophy, retinal 1, caped, central areolar pigment epithelial dystrophy, central retinal pigment epithelial dystrophy.