retinal macular dystrophy type 2 https://www.malacards.org/card/macular_dystrophy_retinal_2 DOID:0070517 macular dystrophy, retinal, 2 MEDGEN:1666864 macular dystrophy, retinal, type 2 MCDR2 MESH:C562746 UMLS:C4749334 GARD:0017467 OMIM:608051 MONDO:0011957 Retinal macular dystrophy type 2 is a rare, genetic macular dystrophy disorder characterized by slowly progressive ''bull's eye'' maculopathy associated, in most cases, with mild decrease in visual acuity and central scotomata. Usually, only the central retina is involved, however some cases of more widespread rod and cone anomalies have been reported. Rare additional features include empty sella turcica, impaired olfaction, renal infections, hematuria and recurrent miscarriages. Orphanet:319640 macular dystrophy, retinal PROM1-related dominant retinopathy