Search Ontology:
Human Disease

torsion dystonia 13

Term ID
DOID:0090037
Synonyms
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)
References
Ontology
Human Disease   ( DOID:0090037 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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