425492002: Generalized dystonia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)

\Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)

\Central nervous system finding\Finding of brain\Disorder of brain\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)

\Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)
\Disease\Disorder of head (disorder)\Disorder of brain\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)
\Disease\Movement disorder\Extrapyramidal disease\Dystonia\Generalized dystonia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2662097011 Generalized dystonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2676185011 Generalized dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2676186012 Generalised dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2662097011 Generalized dystonia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2662097011 Generalized dystonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2676185011 Generalized dystonia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2676185011 Generalized dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2676186012 Generalised dystonia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2676186012 Generalised dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

437651000172119 dystonie généralisée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

437651000172119 dystonie généralisée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Generalized dystonia (disorder)	Is a	Dystonia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Generalized dystonia (disorder)	Finding site	Extrapyramidal system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Generalized dystonia (disorder)	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Developmental malformations-deafness-dystonia syndrome is characterized by the association of midline malformations, sensory hearing loss, and a delayed-onset generalized dystonia syndrome.	Is a	True	Generalized dystonia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
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.	Is a	True	Generalized dystonia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder)	Is a	True	Generalized dystonia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dystonia 28 (disorder)	Is a	True	Generalized dystonia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets