|OBO ID: DOID:0090037|
|Term Name:||torsion dystonia 13||Search Ontology:|
|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. (2)|
|Ontology:||Human Disease (DOID:0090037)|
|is a type of:||
OTHER torsion dystonia 13 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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