Macular Dystrophy, Retinal, 1

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of macular dystrophy associated with mutation(s) in the DNase1 hypersensitivity site DHS6S1.

**Synonyms:** - MCDR1 - NCMD - North Carolina Macular Dystrophy - Retinal Macular Dystrophy-1