(Q32038783)
English
torsion dystonia 13
A dystonia characterized by autosomal dominant inheritance of focal or segmental dystonia with cranial, cervical, or upper limb involvement that has material basis in variation in the chromosome region 1p36.32-p36.13.
- torsion dystonia type 13
- DYSTONIA 13, TORSION, AUTOSOMAL DOMINANT; DYT13
- DYSTONIA 13, TORSION, AUTOSOMAL DOMINANT
- Primary dystonia, DYT13 type
- Primary torsion dystonia with predominant craniocervical or upper limb onset
- Primary dystonia with mixed phenotype
- DYT13
Statements
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Identifiers
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