716664003: Primary dystonia 21 (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du mouvement\Movement disorder\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \constatation à propos d'une région de la tête et du cou\Head finding (finding)\...
• \constatation à propos l'encéphale\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \affection de la tête\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\affection de la tête\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\Familial disease\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\Movement disorder\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)
• \Disease\maladie idiopathique\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia\Primary dystonia 21 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307138011	Primary dystonia 21	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307139015	Primary dystonia DYT21 type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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