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, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995184011	Chylomicron retention disease	en	Synonym	Active	Case insensitive	SNOMED CT core
2995232014	Lipid transport defect of intestine	en	Synonym	Active	Case insensitive	SNOMED CT core
2995490019	Chylomicron retention disease (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2995599016	Anderson syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2995972013	An autosomal recessive disorder of severe fat malabsorption associated with failure to thrive in infancy.	en	Definition	Active	Case sensitive	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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