/Leber congenital amaurosis 17

Leber congenital amaurosis 17

Rare Disease

MONDO:0014145

Also Known As

GDF6 Leber congenital amaurosisLCA17Leber congenital amaurosis 17Leber congenital amaurosis caused by mutation in GDF6Leber congenital amaurosis type 17

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the GDF6 gene.

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Associated Genes

GDF6 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615360 ↗

GARD

GARD:15950 ↗

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