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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.
Mondo Term and Equivalent IDs
MONDO:0010819:  Stargardt disease 3
MESH:C535805: 
UMLS:C1838644: