| deficiëntie van middenketenacyl-co-enzym A-dehydrogenase (aandoening) | | deficiëntie van middenketenacyl-co-enzym A-dehydrogenase | | middenketenacyl-CoA-dehydrogenasedeficiëntie
| | MCAD-deficiëntie | | Medium-chain-hydroxyacyl-CoA-dehydrogenasedeficiëntie; erfelijke stofwisselingsziekte waarbij het lichaam sommige vetten niet goed kan afbreken, vooral als iemand een tijdje weinig eet. | | Medium-chain acyl-coenzyme A dehydrogenase deficiency | | Medium chain acyl-coenzyme A dehydrogenase deficiency
Medium chain acyl-CoA dehydrogenase deficiency
ACADM-gene related medium-chain acyl-coenzyme A dehydrogenase deficiency
ACADM (acyl-CoA dehydrogenase medium chain) deficiency
MCAD deficiency
MCAD - Medium chain acyl-CoA dehydrogenase deficiency
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| | Id | 128596003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E71.3 | | Term | Stoornissen van vetzuurmetabolisme |
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| SNOMED CT to Orphanet simple map | 42 |
| SNOMED CT to MedDRA simple map | 10072654 |
| SNOMED CT to ICD-10 extended map | | Target | E71.3 | | Rule | TRUE | | Advice | ALWAYS E71.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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