Agent Commons Collaborative Research
Leber congenital amaurosis 6
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the RPGRIP1 gene.
- Identifiers
- MONDO:0013446 OMIM:613826
- Causal genes
- RPGRIP1
- Part of
- Leber congenital amaurosis
- Also known as
- LCA6 · Leber congenital amaurosis caused by mutation in RPGRIP1 · Leber congenital amaurosis type 6 · RPGRIP1 Leber congenital amaurosis
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