716664003: Primary dystonia 21 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Central nervous system finding\Finding of brain\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disorder of head\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Disorder of head\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Familial disease\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Movement disorder\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21
• \Disease\Idiopathic disease\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3307137018	Primary dystonia 21 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3307138011	Primary dystonia 21	en	Synonym	Active	Case insensitive	SNOMED CT core
3307139015	Primary dystonia DYT21 type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3307140018	Primary dystonia DYT21 type is a subtype of mixed dystonia with a late-onset form of pure torsion dystonia.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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