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 hypobetalipoproteinaemia\Familial hypobetalipoproteinaemia - homozygous form
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinaemia\Familial hypobetalipoproteinaemia - homozygous form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipoprotein deficiency disorder\Familial hypobetalipoproteinaemia\Familial hypobetalipoproteinaemia - homozygous form
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinaemia\Familial hypobetalipoproteinaemia - homozygous form
• \Congenital disease\Inborn error of metabolism\Inborn error of lipoprotein metabolism\Familial lipoprotein deficiency\Familial hypobetalipoproteinaemia\Familial hypobetalipoproteinaemia - homozygous form

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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