Familial hypercholesterolemia due to genetic defect of apolipoprotein B 403831006
SNOMED CT code
SNOMED code | 403831006 |
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name | Familial hypercholesterolemia due to genetic defect of apolipoprotein B |
status | active |
date introduced | 2003-07-31 |
fully specified name(s) | Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder) |
synonyms |
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attributes - group1 | |
Has interpretation | Above reference range 281302008 |
Interprets | Serum total cholesterol measurement 412808005 |
parents | Familial hypercholesterolemia 398036000 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of lipoprotein AND/OR lipid metabolism 48286001 Disorder of lipoprotein storage and metabolism 238037008 Hyperlipidemia 55822004 Hypercholesterolemia 13644009 Primary hypercholesterolemia 238076009 Familial hypercholesterolemia 398036000 Familial hypercholesterolemia due to genetic defect of apolipoprotein B 403831006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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