5388008: Congenital lactase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Congenital lactase deficiency
• \Metabolic disease\Enzymopathy\Congenital lactase deficiency
• \Metabolic disease\Disorder of carbohydrate metabolism\Disorder of carbohydrate absorption\Lactase deficiency\Congenital lactase deficiency
• \Congenital disease\Congenital lactase deficiency

Status: current, Defined. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
10012014	Congenital lactase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
10013016	Congenital lactose intolerance	en	Synonym	Active	Case insensitive	SNOMED CT core
10014010	Congenital lactose malabsorption	en	Synonym	Active	Case insensitive	SNOMED CT core
10015011	Congenital alactasia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
10016012	Disaccharide intolerance II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
1231260013	Congenital alactasia	en	Synonym	Active	Case insensitive	SNOMED CT core
1231261012	CLD - Congenital lactase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
792049011	Congenital lactase 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

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