Leber congenital amaurosis 7 (Q27677734)
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Leber congenital amaurosis that has material basis in mutation in the CRX gene on chromosome 19q13
- LCA7
- Leber Congenital Amaurosis type 7
- LEBER CONGENITAL AMAUROSIS 7; LCA7
- LEBER CONGENITAL AMAUROSIS 7
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leber congenital amaurosis 7 |
Leber congenital amaurosis that has material basis in mutation in the CRX gene on chromosome 19q13 |
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