Stargardt Disease 3 (STGD3)

Alias:

Stgd3

Macular Dystrophy, Autosomal Dominant, Chromosome 6-Linked

Stargardt-Like Macular Dystrophy

Macular Dystrophy Autosomal Dominant Chromosome 6-Linked

Stargardt-Like Macular Dystrophy, Autosomal Dominant

Macular Dystrophy with Flecks, Type 3

Macular Dystrophy with Flecks Type 3

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Stargardt Disease 3, also known as stgd3, is related to stargardt disease and retinal degeneration. An important gene associated with Stargardt Disease 3 is ELOVL4 (ELOVL Fatty Acid Elongase 4). The drug Metformin has been mentioned in the context of this disorder. Affiliated tissues include retina and skin, and related phenotypes are visual impairment and reduced visual acuity

Related ID：

MALACARDS：STR040

OMIM：600110

MESH：D003317