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Stargardt disease 3 MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
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