| deficiëntie van N-carbamoyl-bèta-alanineamidohydrolase (aandoening) | | deficiëntie van N-carbamoyl-bèta-alanineamidohydrolase | | deficiëntie van bèta-ureidopropionase
| | Deficiency of beta-ureidopropionase |
| | Id | 124511000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E79.8 | | Term | Overige gespecificeerde stoornissen van purine- en pyrimidinemetabolisme |
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| SNOMED CT to Orphanet simple map | 65287 |
| SNOMED CT to ICD-10 extended map | | Target | E88.8 | | Rule | TRUE | | Advice | ALWAYS E88.8 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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