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| Term | dystonia 23 | ID (Ontology) | DOID:0090051 (Human Disease) |
| Definition | A focal dystonia characterized by adult-onset cervical dystonia typically in the fourth or fifth decade of life that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the CACNA1B gene on chromosome 9q34. | ||
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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__ dystonia | |__focal dystonia______________| dystonia 23 |
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| Is a |
autosomal dominant disease focal dystonia |
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External Crossreferences & Linkouts
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ICD10CM:G24.8 MIM:614860 ORDO:420492 |
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