| peroxisomale biogenesestoornis door PEX10-mutatie (aandoening) | | peroxisomale biogenesestoornis door PEX10-mutatie | | peroxisoombiogenesedefect door PEX10-mutatie stoornis in biogenese van peroxisomen door PEX10-mutatie PEX10-deficiƫntie
| | PEX10 deficiency | | Peroxisome biogenesis disorder due to PEX10 mutation
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| | Id | 1187529000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E80.3 | | Term | Katalase- en peroxidasedefecten |
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| SNOMED CT to Orphanet simple map | 247815 |
| SNOMED CT to ICD-10 extended map | | Target | Q87.8 | | Rule | TRUE | | Advice | ALWAYS Q87.8 | 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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