GTR Home > Conditions/Phenotypes > Stargardt disease

Summary

An autosomal recessive and rarely autosomal dominant inherited disorder caused by mutations in the ABCA4 or ELOVL4 genes respectively. It is characterized by macular degeneration that begins in late childhood resulting in progressive loss of vision. [from NCI]

Available tests

4 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

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