718721006: Congenital analbuminemia (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Congenital analbuminemia (disorder)
• \Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital analbuminemia (disorder)
• \Metabolic disease\Hypoproteinemia\Hypoalbuminemia\Congenital analbuminemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3313334013	Congenital analbuminemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313335014	Congenital analbuminemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313336010	Congenital analbuminaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5401839013	Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401840010	Congenital analbuminemia (CAA) is characterised by the absence or dramatic reduction of circulating human serum albumin (HSA).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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