MeSH Browser

MeSH Supplementary: Stargardt disease 3
Unique ID: C535805
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535805
Entry Term(s): Macular dystrophy with flecks, type 3; Macular dystrophy, autosomal dominant, chromosome 6-linked,; Stargardt-Like Macular Dystrophy, Autosomal Dominant
Registry Numbers: 0
Heading Mapped to: Macular Degeneration / congenital
Frequency: 23
Note: A hereditary form of macular degeration. Affected individuals may experience central vision loss as children or young adults and some may also have macular flecks. Mutations have been identified in the ELOVL4 gene. OMIM: 600110
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Stargardt disease 3 MeSH Supplementary Concept Data 2025