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Stargardt disease 4
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any Stargardt disease in which the cause of the disease is a mutation in the PROM1 gene.
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 Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:C535521
OMIM:603786
UMLS:C1863534
MONDO:0011370
High level summary of knowledge for a disease, including descriptions and datasource references.