| deficiëntie van mitochondriaal complex I door deficiëntie van acyl-co-enzym A-dehydrogenase 9 (aandoening) | | deficiëntie van mitochondriaal complex I door deficiëntie van acyl-co-enzym A-dehydrogenase 9 | | mitochondriaal-complex I-deficiëntie door ACAD9-deficiëntie
mitochondriaal-complex I-deficiëntie door acyl-CoA-dehydrogenase 9-deficiëntie
| | Acyl-CoA dehydrogenase 9 deficiency | | Deficiency of acyl-coenzyme A dehydrogenase 9
ACAD9 (acyl-CoA dehydrogenase 9) deficiency
Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9
| | A rare disorder characterized by neurological dysfunction, hepatic failure and cardiomyopathy due to a deficiency of complex I of the respiratory chain. |
| | Id | 725046003 | | 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 | 99901 |
| 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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