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719516000: Autosomal dominant focal dystonia DYT25 type (disorder)


Status: current, Primitive. 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 Initial character case insensitive SNOMED CT core
3316657018 Autosomal dominant focal dystonia DYT25 type en Synonym Active Initial character case insensitive SNOMED CT core
3316658011 A form of focal dystonia with characteristics of cervical, laryngeal and hand-forearm dystonia. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant focal dystonia DYT25 type Interprets Movement true Inferred relationship Some 2
Autosomal dominant focal dystonia DYT25 type Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant focal dystonia DYT25 type Is a Hereditary disorder of nervous system true Inferred relationship Some
Autosomal dominant focal dystonia DYT25 type Is a Focal dystonia true Inferred relationship Some
Autosomal dominant focal dystonia DYT25 type Finding site Extrapyramidal system structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Strength reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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