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782695002: Primary dystonia DYT17 type (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
5405649018 Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalized dystonia. Dysphonia and dysarthria also occur later in the disease course. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5405650018 Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalised dystonia. Dysphonia and dysarthria also occur later in the disease course. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755250010 Primary dystonia DYT17 type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3755251014 Primary dystonia DYT17 type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6466231000241112 dystonie primaire de type 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6466241000241119 dystonie primaire de type DYT17 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443581001000114 Dystonie, primäre, Typ DYT17 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
Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalized dystonia. Dysphonia and dysarthria also occur later in the disease course. Is a Autosomal recessive idiopathic familial dystonia true Inferred relationship Some
Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalized dystonia. Dysphonia and dysarthria also occur later in the disease course. Finding site Extrapyramidal system structure (body structure) true Inferred relationship Some 1
Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalized dystonia. Dysphonia and dysarthria also occur later in the disease course. Interprets mouvement false Inferred relationship Some 2
Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalized dystonia. Dysphonia and dysarthria also occur later in the disease course. Interprets Movement observable true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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