Search Ontology:
Human Disease

torsion dystonia 1

Term ID
DOID:0060730
Synonyms
Definition
A generalized dystomia characterized by autosomal dominant inheritance of dystonia usually presenting initially as focal, typically in the limbs, but often generalizes with age that has_material_basis_in heterozygous mutation in the TOR1A gene on chromosome 9q34. (2)
References
Ontology
Human Disease   ( DOID:0060730 )
Relationships
is a type of
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Genes Involved
Zebrafish Models