403831006: Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level (finding)\Lipid level - finding\...
• \Serum lipid levels - finding\Serum cholesterol level - finding\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Serum lipid levels - finding\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Cholesterol level - finding\Serum cholesterol level - finding\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Lipids abnormal\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Lipids abnormal\Increased lipid\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Lipids abnormal\Increased lipid\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Measurement finding outside reference range\Lipids abnormal\Serum cholesterol abnormal\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Measurement finding outside reference range\Lipids abnormal\Increased lipid\Serum lipids high\taux de cholestérol sérique augmenté\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Measurement finding outside reference range\Lipids abnormal\Increased lipid\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
• \Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\troubles du stockage et du métabolisme des lipoprotéines\hyperlipidémie\hypercholestérolémie\hypercholestérolémie primitive\Familial hypercholesterolemia (disorder)\Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1771757017	Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773759012	Familial hypercholesterolaemia due to genetic defect of apolipoprotein B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1775045012	Familial hypercholesterolemia due to genetic defect of apolipoprotein B	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1783803018	Hypercholesterolaemia due to apolipoprotein B gene defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1784188017	Hypercholesterolemia due to apolipoprotein B gene defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1784189013	Familial Combined Hypercholesterolemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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