Leber congenital amaurosis 12 (Q27677618)
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Leber congenital amaurosis that has material basis in mutation in the RD3 gene on chromosome 1q32
- LCA12
- Leber Congenital Amaurosis type 12
- LEBER CONGENITAL AMAUROSIS 12
- LEBER CONGENITAL AMAUROSIS 12; LCA12
- Amaurosis congenita of Leber, type 12
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leber congenital amaurosis 12 |
Leber congenital amaurosis that has material basis in mutation in the RD3 gene on chromosome 1q32 |
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