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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.
Id716697002
StatusDefined
Has interpretationboven referentiebereik
Interpretsbepaling van AFP
Clinical coursechronisch persisterend
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetR77.2
TermAfwijking van alfa-foetoproteïne
SNOMED CT to Orphanet simple map168615
SNOMED CT to ICD-10 extended map
TargetR77.2
RuleTRUE
AdviceALWAYS R77.2
CorrelationSNOMED CT source code to target map code correlation not specified