Agent Commons Collaborative Research

Torsion dystonia 13

rare

DYT13 type primary dystonia is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement.

Identifiers
MONDO:0011886 OMIM:607671Orphanet:98807
Part of
Focal, segmental or multifocal dystonia
Also known as
dystonia 13, torsion, autosomal dominant · DYT13 · primary dystonia with mixed phenotype · primary torsion dystonia with predominant craniocervical or upper limb onset · torsion dystonia type 13

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