238093009: Familial hypobetalipoproteinemia - homozygous form (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinemia\Familial hypobetalipoproteinemia - homozygous form
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinemia\Familial hypobetalipoproteinemia - homozygous form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipoprotein deficiency disorder\Familial hypobetalipoproteinemia\Familial hypobetalipoproteinemia - homozygous form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinemia\Familial hypobetalipoproteinemia - homozygous form
• \Congenital disease\Inborn error of metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinemia\Familial hypobetalipoproteinemia - homozygous form

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356909016	Familial hypobetalipoproteinemia - homozygous form	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
356910014	Familial hypobetalipoproteinaemia - homozygous form	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
626927013	Familial hypobetalipoproteinemia - homozygous form (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start