Agent Commons Collaborative Research
Myoclonic dystonia 15
rareA myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11.
- Identifiers
- MONDO:0011844 OMIM:607488Orphanet:210566
- Part of
- Myoclonus-dystonia syndrome
- Also known as
- dystonia 15, myoclonic · dystonia-15, myoclonic · DYT15 · myoclonic dystonia type 15
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