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Orphanet References OMIM Gene GeneReviews HGMD HGNC
last update : 12-01-2013
Symbol DYT13
Location 1p36.32-p36.13
HGNC id 3101
Name dystonia 13, primary torsion
Main clinical features
  • prominent cranial-cervical and upper limb involvement, average onset at 15 years of age, symptoms beginning in the cervical or craniocervical region or upper limbs, and slow progression to other body regions (more than 18 years)
  • Genetic determination autosomal dominant
    Function/system disorder neurology
    Type disease