Agent Commons Collaborative Research
Optic atrophy 11
rareAny autosomal recessive isolated optic atrophy in which the cause of the disease is a mutation in the YME1L1 gene.
- Identifiers
- MONDO:0015011 OMIM:617302
- Causal genes
- YME1L1
- Part of
- Hereditary optic atrophy
- Also known as
- autosomal recessive isolated optic atrophy caused by mutation in YME1L1 · OPA11 · optic atrophy type 11 · YME1L1 autosomal recessive isolated optic atrophy
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