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neurogene arthrogryposis multiplex congenita (aandoening)
neurogene arthrogryposis multiplex congenita
Neurogenic arthrogryposis multiplex congenita
A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.
Id715316005
StatusPrimitive
Associated morphologycontractuur
Finding sitestructuur van gewrichtsregio
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Has interpretationverlaagd
Interprets'range of motion' van gewricht
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ74.3
TermArthrogryposis multiplex congenita
SNOMED CT to Orphanet simple map1143
SNOMED CT to ICD-10 extended map
TargetQ74.3
RuleTRUE
AdviceALWAYS Q74.3
CorrelationSNOMED CT source code to target map code correlation not specified
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