Leber congenital amaurosis 15 (Q27674860)
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A Leber congenital amaurosis that has material basis in mutation in the TULP1 gene on chromosome 6p21.3.
- LCA15
- LEBER CONGENITAL AMAUROSIS 15; LCA15
- LEBER CONGENITAL AMAUROSIS 15
- Leber Congenital Amaurosis type 15
- Retinitis Pigmentosa, Juvenile, Tulp1-Related
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Leber congenital amaurosis 15 |
A Leber congenital amaurosis that has material basis in mutation in the TULP1 gene on chromosome 6p21.3. |
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