| deficiëntie van glutaryl-co-enzym A-oxidase (aandoening) | | deficiëntie van glutaryl-co-enzym A-oxidase | | glutaryl-CoA-oxidasedeficiëntie
glutaryl-co-enzym A-oxidasedeficiëntie
|  | Dit betekent dat je lichaam bepaalde stoffen niet goed kan afbreken. Daarom kunnen schadelijke stoffen zich in je lichaam ophopen. Dat kan leiden tot allerlei problemen met je gezondheid. | | Glutaryl-CoA oxidase deficiency | | SUGCT-gene related glutaryl-coenzyme A oxidase deficiency
Glutaryl-coenzyme A oxidase deficiency
Glutaric acidemia type 3
Glutaric aciduria type 3
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| | Id | 238070003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E72.3 | | Term | Stoornissen van lysine- en hydroxylysinemetabolisme |
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| SNOMED CT to Orphanet simple map | 35706 |
| SNOMED CT to ICD-10 extended map | | Target | E72.8 | | Rule | TRUE | | Advice | ALWAYS E72.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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