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719516000: Autosomal dominant focal dystonia DYT25 type (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3316656010 Autosomal dominant focal dystonia DYT25 type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3316657018 Autosomal dominant focal dystonia DYT25 type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402143011 A form of focal dystonia characterized by cervical, laryngeal and hand-forearm dystonia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402144017 A form of focal dystonia characterised by cervical, laryngeal and hand-forearm dystonia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant focal dystonia DYT25 type (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant focal dystonia DYT25 type (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Autosomal dominant focal dystonia DYT25 type (disorder) Is a Focal dystonia (disorder) true Inferred relationship Some
Autosomal dominant focal dystonia DYT25 type (disorder) Finding site Extrapyramidal system structure true Inferred relationship Some 1
Autosomal dominant focal dystonia DYT25 type (disorder) Interprets Movement 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)

GB English

US English

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