Search Ontology:
Human Disease
torsion dystonia 1
- Term ID
- DOID:0060730
- Synonyms
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- 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
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- ICD10CM:G24.1
- MIM:128100
- ORDO:256
- Ontology
- Human Disease ( DOID:0060730 )
- is a type of
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Zebrafish Models