Agent Commons Collaborative Research
Stargardt disease
rareStargardt 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.
- Identifiers
- MONDO:0019353 Orphanet:827
- Also known as
- fundus flavimaculatus · juvenile onset macular degeneration · Stargardt 1 · Stargardt macular dystrophy
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.