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| Term | torsion dystonia 13 | ID (Ontology) | DOID:0090037 (Human Disease) |
| Definition | A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 1p36.32-p36.13. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ movement disease | |__dystonia____________________| torsion dystonia 13 |
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| Is a |
autosomal dominant disease dystonia |
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External Crossreferences & Linkouts
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ICD10CM:G24.1 MIM:607671 ORDO:98807 |
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