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familiaire hypobètalipoproteïnemie - homozygote vorm (aandoening)
familiaire hypobètalipoproteïnemie - homozygote vorm
familiale hypobètalipoproteïnemie - homozygote vorm
Familial hypobetalipoproteinemia - homozygous form
Id238093009
StatusPrimitive
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE78.6
TermLipoproteïnedeficiëntie
SNOMED CT to ICD-10 extended map
TargetE78.6
RuleTRUE
AdviceALWAYS E78.6
CorrelationSNOMED CT source code to target map code correlation not specified