702364003: Chylomicron retention disease (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Chylomicron retention disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995184011	Chylomicron retention disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2995232014	Lipid transport defect of intestine	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2995490019	Chylomicron retention disease (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2995599016	Anderson syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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