Visualize Submit Comment
Metadata
ID DOID:0090037
Name torsion dystonia 13
Definition A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 1p36.32-p36.13.
https://www.ncbi.nlm.nih.gov/pubmed/11261511, https://www.omim.org/entry/607671
Xrefs

ICD10CM:G24.1

OMIM:607671

ORDO:98807

Subsets

DO_rare_slim

Parent Relationships

is_a dystonia

is_a autosomal dominant disease

Add an item to the term tracker