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Human Disease
dystonia 23
- Term ID
- DOID:0090051
- Synonyms
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- 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. (2)
- References
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- ICD10CM:G24.8
- MIM:614860
- ORDO:420492
- Ontology
- Human Disease ( DOID:0090051 )
- is a type of
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