Leber congenital amaurosis 3 (Q27677732)
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Leber congenital amaurosis that has material basis in mutation in the SPATA7 gene on chromosome 14q31
- LCA3
- Retinitis Pigmentosa, Juvenile, Spata7-Related
- LEBER CONGENITAL AMAUROSIS 3; LCA3
- Amaurosis congenita of Leber, type 3
- Leber congenital amaurosis type 3
- LEBER CONGENITAL AMAUROSIS 3
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leber congenital amaurosis 3 |
Leber congenital amaurosis that has material basis in mutation in the SPATA7 gene on chromosome 14q31 |
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