| fatale infantiele deficiëntie van cytochroom c-oxidase (aandoening) | | fatale infantiele deficiëntie van cytochroom c-oxidase | | fatale infantiele cytochroom c-oxidasedeficiëntie
| | Fatal infantile cytochrome C oxidase deficiency | | A very rare mitochondrial disease with clinical characteristic of cardioencephalomyopathy resulting in death in infancy. |
| | Id | 718124006 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G71.3 | | Term | Mitochondriën-myopathie, niet elders geclassificeerd |
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| SNOMED CT to Orphanet simple map | 1561 |
| SNOMED CT to ICD-10 extended map | | Target | G71.3 | | Rule | TRUE | | Advice | ALWAYS G71.3 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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