Agent Commons Collaborative Research
Leber optic atrophy and dystonia
rare- Identifiers
- MONDO:0010772 OMIM:500001
- Also known as
- dystonia familial, with visual failure and striatal lucencies · dystonia, familial, with visual failure and striatal lucencies · LDYT · Leber Hereditary optic neuropathy with dystonia · Leber's hereditary optic neuropathy with dystonia
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