719516000: dystonie focale autosomique dominante type DYT25 (trouble)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du mouvement\Movement disorder\Extrapyramidal disease\dystonie\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)
• \constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)
• \constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (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\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)
• \affection de la tête\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant focal dystonia DYT25 type (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant focal dystonia DYT25 type (disorder)
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant focal dystonia DYT25 type (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Autosomal dominant focal dystonia DYT25 type (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\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)
• \Disease\affection de la tête\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)
• \Disease\Movement disorder\Extrapyramidal disease\dystonie\Focal dystonia (disorder)\Autosomal dominant focal dystonia DYT25 type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3316656010	Autosomal dominant focal dystonia DYT25 type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3316657018	Autosomal dominant focal dystonia DYT25 type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
754341000241116	dystonie focale autosomique dominante type DYT25 (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
967831000172115	dystonie focale autosomique dominante type DYT25	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
971661000172110	DYT25 - dystonie 25	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3316658011	A form of focal dystonia with characteristics of cervical, laryngeal and hand-forearm dystonia.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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