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230319002: Autosomal dominant idiopathic familial dystonia (disorder)


Status: current, Defined. Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345147014 Autosomal dominant idiopathic familial dystonia en Synonym Active Case insensitive SNOMED CT core
618109017 Autosomal dominant idiopathic familial dystonia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
THAP1 dystonia Is a True Autosomal dominant idiopathic familial dystonia Inferred relationship Some
Primary dystonia 21 Is a True Autosomal dominant idiopathic familial dystonia Inferred relationship Some
Primary dystonia DYT4 type Is a True Autosomal dominant idiopathic familial dystonia Inferred relationship Some
Primary dystonia DYT13 type Is a True Autosomal dominant idiopathic familial dystonia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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