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. |
| Id | 715316005 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | Target | Q74.3 | Term | Arthrogryposis multiplex congenita |
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SNOMED CT to Orphanet simple map | 1143 |
SNOMED CT to ICD-10 extended map | Target | Q74.3 | Rule | TRUE | Advice | ALWAYS Q74.3 | Correlation | SNOMED CT source code to target map code correlation not specified |
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