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Myoclonic dystonia 26
rareAny myoclonus-dystonia syndrome in which the cause of the disease is a mutation in the KCTD17 gene.
- Identifiers
- MONDO:0014620 OMIM:616398
- Causal genes
- KCTD17
- Part of
- Myoclonus-dystonia syndrome
- Also known as
- dystonia 26, myoclonic · DYT26 · KCTD17 myoclonus-dystonia syndrome · myoclonic dystonia type 26 · myoclonus-dystonia syndrome caused by mutation in KCTD17
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