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| Term | torsion dystonia 4 | ID (Ontology) | DOID:0090041 (Human Disease) |
| Definition | A dystonia that is characterized by progressive laryngeal and cervical dystonia (onset in the second to third decade of life) followed by involvement of other muscles, such as the neck or limbs that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 4A class IVa (TUBB4A) gene on chromosome 19p13. | ||
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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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autosomal genetic disease |__autosomal dominant disease__ movement disease | |__dystonia____________________| torsion dystonia 4 4 rec. |
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autosomal dominant disease dystonia |
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ICD10CM:G24.1 MIM:128101 ORDO:98805 |
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