Dystonia 13, Torsion, Autosomal Dominant (DYT13)

Alias:

Dystonia 13, Torsion

Dyt13

Primary Torsion Dystonia with Predominant Craniocervical or Upper Limb Onset

Primary Dystonia with Mixed Phenotype

Primary Dystonia, Dyt13 Type

Torsion Dystonia 13

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Dystonia 13, Torsion, Autosomal Dominant, also known as dystonia 13, torsion, is related to dystonia and dystonia 1, torsion, autosomal dominant, and has symptoms including dystonia, torticollis and tremor. An important gene associated with Dystonia 13, Torsion, Autosomal Dominant is DYT13 (Dystonia 13, Torsion). Related phenotypes are involuntary movements and torsion dystonia

Related ID：

MALACARDS：DYS185

OMIM：607671