Stargardt disease
MONDO:0019353Also known as: Stargardt 1, fundus flavimaculatus, Stargardt disease 1, Stargardt macular dystrophy, juvenile onset macular degeneration
- MONDO:
- MONDO:0019353
- Orphanet:
- 827 ↗
Rare disease87 associated genes
Description
Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion.
Associated genes
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