Disease association ontology term - MONDO:0019353 - Stargardt disease
Term summary
- ID
- MONDO:0019353
- Name
- Stargardt disease
- Ontology or CV name
- Disease association
- Definition
- 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.
