Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder) | | Familial hypercholesterolemia due to genetic defect of apolipoprotein B | | Familial Combined Hypercholesterolemia Hypercholesterolemia due to apolipoprotein B gene defect
| | familiaire hypercholesterolemie door genetisch defect van apolipoproteïne B | | familiale hypercholesterolemie door genetisch defect van apolipoproteïne B familiaire hypercholesterolemie door genetisch defect van apo-B
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| Id | 403831006 | Status | Primitive |
ICD-10 complex map reference set | Target | E78.0 | Rule | TRUE | Advice | ALWAYS E78.0 | Correlation | SNOMED CT source code to target map code correlation not specified |
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