715777007: Primary dystonia type 2 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of movement\Movement disorder\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Central nervous system finding\Finding of brain\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disorder of head\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Disorder of head\Encephalopathy\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Familial disease\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Movement disorder\Extrapyramidal disease\Dystonia\Torsion dystonia\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2
• \Disease\Idiopathic disease\Primary torsion dystonia\Idiopathic familial dystonia\Autosomal recessive idiopathic familial dystonia\Primary dystonia type 2

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3303681014	Primary dystonia type 2 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3303682019	Primary dystonia type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
3303683012	Primary dystonia DYT2 type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3303684018	Segmental dystonia that manifests with involuntary posturing affecting predominantly the feet. The exact prevalence is unknown. The disease is reported in a limited number of Jewish and Gypsy families. The onset of the symptoms is early in childhood or adolescence.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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