230310003: Paroxysmal dystonia (disorder)

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

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

\Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Paroxysmal dystonia

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

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

345136019 Paroxysmal dystonia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

618099014 Paroxysmal dystonia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

235791000077115 dystonie paroxystique 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
Paroxysmal dystonia	Is a	Kinesiogenic choreoathetosis	false	Inferred relationship	Some
Paroxysmal dystonia	Is a	Dystonia	true	Inferred relationship	Some
Paroxysmal dystonia	Finding site	Structure of basal nucleus	false	Inferred relationship	Some
Paroxysmal dystonia	Onset	Sudden	false	Inferred relationship	Some
Paroxysmal dystonia	Onset	Sudden onset	false	Inferred relationship	Some
Paroxysmal dystonia	Is a	Acute nervous system disorder	false	Inferred relationship	Some
Paroxysmal dystonia	Clinical course	Sudden onset AND/OR short duration (qualifier value)	false	Inferred relationship	Some
Paroxysmal dystonia	Is a	Chronic nervous system disorder	false	Inferred relationship	Some
Paroxysmal dystonia	Clinical course	Paroxysmal	true	Inferred relationship	Some	1
Paroxysmal dystonia	Finding site	Extrapyramidal system structure (body structure)	true	Inferred relationship	Some	2
Paroxysmal dystonia	Is a	Chronic brain syndrome	false	Inferred relationship	Some
Paroxysmal dystonia	Interprets	mouvement	false	Inferred relationship	Some	3
Paroxysmal dystonia	Interprets	Movement observable	true	Inferred relationship	Some	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder)	Is a	True	Paroxysmal dystonia	Inferred relationship	Some
A paroxysmal dystonic movement disorder occurring in association with gastro-oesophageal reflux, and, in some cases, hiatal hernia. The prevalence is unknown. Onset usually occurs during infancy or early childhood. The dystonic movements are characterised by abnormal posturing of the head and neck (torticollis) and severe arching of the spine. The dystonic movements are clearly associated with gastro-oesophageal reflux but the pathophysiological mechanism is not clearly understood.	Is a	True	Paroxysmal dystonia	Inferred relationship	Some
A rare, transient paroxysmal dystonia characterized by onset of recurrent episodes of torticollis posturing of the head between infancy and early-childhood.	Is a	True	Paroxysmal dystonia	Inferred relationship	Some
Paroxysmal exertion-induced dyskinesia (PED) is a form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities.	Is a	True	Paroxysmal dystonia	Inferred relationship	Some
A rare genetic epilepsy syndrome characterized by infantile or childhood onset of focal motor seizures remitting with age, as well as childhood onset of exercise-induced dystonia which often persists into adulthood. Additional reported features include nystagmus and postural tremor of the hands.	Is a	True	Paroxysmal dystonia	Inferred relationship	Some

This concept is not in any reference sets