(Q27677590)
English
Leber congenital amaurosis 2
Leber congenital amaurosis that is characterized by night blindness, some transient improvement in vision, and eventual progressive visual loss and has material basis in mutation in the RPE65 gene on chromosome 1
- LCA2
- amaurosis congenita of Leber II
- Amaurosis Congenita of Leber 2
- LEBER CONGENITAL AMAUROSIS 2; LCA2
- LEBER CONGENITAL AMAUROSIS 2
- Leber Congenital Amaurosis type 2
- Amaurosis congenita of Leber, type 2
Statements
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Identifiers
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