312857009: Alpha-2-antitrypsin deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Glycoprotein metabolism disorder\Alpha-2 antitrypsin deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Glycoprotein metabolism disorder\Alpha-2 antitrypsin deficiency
• \Congenital disease\Inborn error of metabolism\Glycoprotein metabolism disorder\Alpha-2 antitrypsin deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2030981000168113	Alpha-2 antitrypsin deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED Clinical Terms Australian extension
2030991000168111	A2AT (alpha-2 antitrypsin) deficiency	en	Synonym	Active	Case sensitive	SNOMED Clinical Terms Australian extension
456647010	Alpha-2-antitrypsin deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
709574016	Alpha-2-antitrypsin deficiency (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

Back to Start