familiaire hypercholesterolemie
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familiaire hypercholesterolemie door genetisch defect van apolipoproteïne B (aandoening)
familiaire hypercholesterolemie door genetisch defect van apolipoproteïne B
familiaire hypercholesterolemie door genetisch defect van apo-B
familiale hypercholesterolemie door genetisch defect van apolipoproteïne B
Familial hypercholesterolemia due to genetic defect of apolipoprotein B
Hypercholesterolemia due to apolipoprotein B gene defect
Id403831006
StatusPrimitive
Has interpretationboven referentiebereik
Interpretsbepalen van totaal cholesterol in serum
SNOMED CT to ICD-10 extended map
TargetE78.0
RuleTRUE
AdviceALWAYS E78.0
CorrelationSNOMED CT source code to target map code correlation not specified