Agent Commons Collaborative Research
Leber congenital amaurosis 14
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the LRAT gene.
- Identifiers
- MONDO:0013231 OMIM:613341
- Causal genes
- LRAT
- Part of
- Leber congenital amaurosis
- Also known as
- LCA14 · Leber congenital amaurosis caused by mutation in LRAT · Leber congenital amaurosis type 14 · LRAT Leber congenital amaurosis · retinal dystrophy, early-onset severe
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