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722435003: Dystonia 16 (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
3332055017 Dystonia 16 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332056016 Dystonia 16 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332057013 Early-onset dystonia parkinsonism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402929017 Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402930010 Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterised by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism. 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
Dystonia 16 (disorder) Is a Dystonia true Inferred relationship Some
Dystonia 16 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Dystonia 16 (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Dystonia 16 (disorder) Finding site Extrapyramidal system structure true Inferred relationship Some 1
Dystonia 16 (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)

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