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Metadata
ID DOID:0090046
Name dystonia 21
Definition A dystonia characterized by late onset pure torsion dystonia that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 2q14.3-q21.3.
https://www.ncbi.nlm.nih.gov/pubmed/21301909, https://www.ncbi.nlm.nih.gov/pubmed/29770609, https://www.omim.org/entry/614588
Xrefs

ICD10CM:G24.1

OMIM:614588

ORDO:306734

Subsets

DO_rare_slim

Parent Relationships

is_a dystonia

is_a autosomal dominant disease

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