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Metadata
ID DOID:0090036
Name myoclonic dystonia 26
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.
https://ghr.nlm.nih.gov/condition/myoclonus-dystonia, https://www.omim.org/entry/616398
Xrefs

OMIM:616398

Parent Relationships

is_a myoclonic dystonia

is_a autosomal dominant disease

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