| congenitale analbuminemie (aandoening) | | congenitale analbuminemie | | Congenital analbuminemia | | Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA). |
| | Id | 718721006 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E88.0 | | Term | Stofwisselingsstoornissen van plasmaproteïne, niet elders geclassificeerd |
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| SNOMED CT to Orphanet simple map | 86816 |
| SNOMED CT to ICD-10 extended map | | Target | R77.0 | | Rule | TRUE | | Advice | ALWAYS R77.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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