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| Term | torsion dystonia 17 | ID (Ontology) | DOID:0090042 (Human Disease) |
| Definition | A dystonia that is characterized by progressive dystonia, dysphonia, dysarthria and neck torticollis, and has_material_basis_in autosomal recessive inheritance of variation in the chromosome region 20p11.2-q13.12. | ||
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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 recessive disease__ movement disease | |__dystonia_____________________| torsion dystonia 17 |
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| Is a |
autosomal recessive disease dystonia |
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External Crossreferences & Linkouts
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ICD10CM:G24.1 MIM:612406 ORDO:370103 |
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