You are using an outdated browser. Please upgrade your browser to improve your experience.
Stargardt disease 3
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description A common hereditary macular degeneration. It is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:C535805
OMIM:600110
UMLS:C1838644
MONDO:0010819
High level summary of knowledge for a disease, including descriptions and datasource references.