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724383002: Hemidystonia hemiatrophy syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3434947014 Hemidystonia hemiatrophy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434948016 Hemidystonia hemiatrophy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403321017 Hemidystonia-hemiatrophy (HD-HA) is a rare dystonia, usually caused by a static cerebral injury occurring at birth or during infancy, that is characterized by a combination of hemidystonia (HD), involving one half of the body, and hemiatrophy (HA) on the same side as the HD. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403322012 Hemidystonia-hemiatrophy (HD-HA) is a rare dystonia, usually caused by a static cerebral injury occurring at birth or during infancy, that is characterised by a combination of hemidystonia (HD), involving one half of the body, and hemiatrophy (HA) on the same side as the HD. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3434947014 Hemidystonia hemiatrophy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434948016 Hemidystonia hemiatrophy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434949012 A rare dystonia with a combination of hemidystonia involving one half of the body and hemiatrophy on the same side. Hemidystonia which is sustained and repetitive muscle contractions resulting in abnormal movements or posture involving a single side of the body is preceded in 90% of cases by hemiparesis with a marked improvement before the onset of hemidystonia. Pyramidal syndrome and seizures may also be observed. The syndrome is associated with ipsilateral somatic atrophy. Common causes are childbirth or perinatal complications, delayed sequelae of stroke or head trauma. This syndrome should be differentiated from other causes of primary dystonia or dystonia secondary to inherited disorders or neurodegenerative diseases. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403321017 Hemidystonia-hemiatrophy (HD-HA) is a rare dystonia, usually caused by a static cerebral injury occurring at birth or during infancy, that is characterized by a combination of hemidystonia (HD), involving one half of the body, and hemiatrophy (HA) on the same side as the HD. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403322012 Hemidystonia-hemiatrophy (HD-HA) is a rare dystonia, usually caused by a static cerebral injury occurring at birth or during infancy, that is characterised by a combination of hemidystonia (HD), involving one half of the body, and hemiatrophy (HA) on the same side as the HD. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431381001000118 Hemidystonie-Hemiatrophie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6256231000241115 syndrome HD-HA (hémidystonie-hémiatrophe) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6256241000241113 syndrome d'hémidystonie et hémiatrophie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6256231000241115 syndrome HD-HA (hémidystonie-hémiatrophe) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6256241000241113 syndrome d'hémidystonie et hémiatrophie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431381001000118 Hemidystonie-Hemiatrophie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemidystonia hemiatrophy syndrome (disorder) Is a Degenerative disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hemidystonia hemiatrophy syndrome (disorder) Is a Hemidystonia true Inferred relationship Existential restriction modifier (core metadata concept)
Hemidystonia hemiatrophy syndrome (disorder) Finding site Extrapyramidal system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hemidystonia hemiatrophy syndrome (disorder) Associated morphology Hemiatrophy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hemidystonia hemiatrophy syndrome (disorder) Finding site Structure of half of body lateral to midsagittal plane true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hemidystonia hemiatrophy syndrome (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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