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Myoclonic dystonia 15

MONDO:0011844

A myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11.

Also known as: dystonia-15, myoclonic, myoclonic dystonia type 15, DYT15, dystonia 15, myoclonic

14 clinical trials for this condition and its sub-types, 0 tagged with Myoclonic dystonia 15 itself.

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