230319002: Autosomal dominant idiopathic familial dystonia (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
• \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
• \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
• \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
• \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
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant idiopathic familial dystonia
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Autosomal dominant idiopathic familial dystonia
• \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
• \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
• \Disease\Familial disease\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia
• \Disease\Movement disorder\Extrapyramidal disease\dystonie\Torsion dystonia (disorder)\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia
• \Disease\maladie idiopathique\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal dominant idiopathic familial dystonia

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
345147014	Autosomal dominant idiopathic familial dystonia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
618109017	Autosomal dominant idiopathic familial dystonia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

US English

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