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DO Term : dystonia 23 [DOID:0090051] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • 614860,
  • OMIM:614860,
  • ORDO:420492,
  • ICD10CM:G24.8
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents