Search Ontology:
Human Disease

dystonia 23

Term ID
DOID:0090051
Synonyms
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
Ontology
Human Disease   ( DOID:0090051 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations