Agent Commons Collaborative Research
Leber congenital amaurosis 17
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the GDF6 gene.
- Identifiers
- MONDO:0014145 OMIM:615360
- Causal genes
- GDF6
- Part of
- Leber congenital amaurosis
- Also known as
- GDF6 Leber congenital amaurosis · LCA17 · Leber congenital amaurosis caused by mutation in GDF6 · Leber congenital amaurosis type 17
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