myoclonic dystonia 26 (DOID:0090036)
Alliance: disease page
Alt IDs: OMIM:616398
Definition: A myoclonic dystonia characterized by onset of myoclonic jerks affecting the upper limbs, progressing to dystonia with predominant involvement of the craniocervical regions, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the KCTD17 gene on chromosome 22q12.