| hereditaire coproporfyrie (aandoening) | | hereditaire coproporfyrie | | Hereditary coproporphyria | | HCP - Hereditary coproporphyria
Coproporphyrinogen oxidase deficiency
Berger-Goldberg syndrome
CPO deficiency
CPO - Coproporphyrinogen oxidase deficiency
Porphyria hepatica II
CPRO deficiency
|
| | DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E80.2 | | Term | Overige gespecificeerde vormen van porfyrie |
| Target | Z83.4 | | Term | Familie-anamnese met overige endocriene ziekten en voedings- en stofwisselingsstoornissen |
|
| SNOMED CT to Orphanet simple map | 79273 |
| SNOMED CT to ICD-10 extended map | | Target | E80.2 | | Rule | TRUE | | Advice | ALWAYS E80.2 | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
