hereditaire persistentie van alfafoetoproteïne (aandoening) | | hereditaire persistentie van alfafoetoproteïne | | erfelijke persistentie van AFP
| | Hereditary persistence of alpha-fetoprotein | | A benign genetic condition with characteristic of persistence of high alpha-fetoprotein (AFP) levels throughout life, with no associated clinical disability and thus no need for specific therapy. |
| DHD Diagnosis thesaurus reference set |
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | Target | R77.2 | Term | Afwijking van alfa-foetoproteïne |
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SNOMED CT to Orphanet simple map | 168615 |
SNOMED CT to ICD-10 extended map | Target | R77.2 | Rule | TRUE | Advice | ALWAYS R77.2 | Correlation | SNOMED CT source code to target map code correlation not specified |
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