Autosomal recessive idiopathic familial dystonia
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Primary dystonia DYT17 type (disorder)
Primary dystonia DYT17 type
Primary dystonia, DYT17 type is a rare, genetic, isolated dystonia initially presenting as torticollis, and later progressing to segmental or generalized dystonia. Dysphonia and dysarthria also occur later in the disease course.
Id782695002
StatusPrimitive
Finding siteExtrapyramidal system structure
InterpretsMovement observable
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetG24.1
TermIdiopathische familiale dystonie
SNOMED CT to ICD-10 extended map
TargetG24.1
RuleTRUE
AdviceALWAYS G24.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified