782718007: Dystonia aphonia syndrome (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du mouvement\Movement disorder\Extrapyramidal disease\dystonie\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)
• \constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)
• \constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Generalized dystonia (disorder)\Dystonia aphonia syndrome (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\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)
• \affection de la tête\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)
• \constatation fonctionnelle\trouble de communication\Speech and language disorder\Aphonia (disorder)\Dystonia aphonia syndrome (disorder)
• \constatation à propos de la parole\Speech and language finding\constatation à propos de la communication, de l'élocution et du langage\trouble de communication\Speech and language disorder\Aphonia (disorder)\Dystonia aphonia syndrome (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Dystonia aphonia syndrome (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Dystonia aphonia syndrome (disorder)
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Dystonia aphonia syndrome (disorder)
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Dystonia aphonia syndrome (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\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)
• \Disease\trouble de communication\Speech and language disorder\Aphonia (disorder)\Dystonia aphonia syndrome (disorder)
• \Disease\affection de la tête\Disorder of brain (disorder)\Extrapyramidal disease\dystonie\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)
• \Disease\Movement disorder\Extrapyramidal disease\dystonie\Generalized dystonia (disorder)\Dystonia aphonia syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3755457010	Dystonia aphonia syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3755458017	Dystonia aphonia syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3755459013	A rare genetic persistent combined dystonia disorder characterized by slowly progressive severe caudo-rostrally spreading generalized dystonia with prominent facial and oro-mandibular involvement leading to severe anarthria and/or aphonia, swallowing difficulties and gait disturbances. Additional manifestations include slowed horizontal saccades, subclinical epilepsy, photic myoclonus, oral hypertrophic changes (for example gingival or lingual hyperplasia) as well as delayed milestones and cognitive impairment.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3755460015	A rare genetic persistent combined dystonia disorder characterised by slowly progressive severe caudo-rostrally spreading generalised dystonia with prominent facial and oro-mandibular involvement leading to severe anarthria and/or aphonia, swallowing difficulties and gait disturbances. Additional manifestations include slowed horizontal saccades, subclinical epilepsy, photic myoclonus, oral hypertrophic changes (for example gingival or lingual hyperplasia) as well as delayed milestones and cognitive impairment.	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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