/Leber congenital amaurosis 16

Leber congenital amaurosis 16

Rare Disease

MONDO:0013613

Also Known As

KCNJ13 Leber congenital amaurosisLCA16Leber congenital amaurosis 16Leber congenital amaurosis caused by mutation in KCNJ13Leber congenital amaurosis type 16

Definition

Any Leber congenital amaurosis in which the cause of the disease is a mutation in the KCNJ13 gene.

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Associated Genes

KCNJ13 ↗

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

External Resources

OMIM

OMIM:614186 ↗

GARD

GARD:10885 ↗

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