27943000: Congenital glucose-galactose malabsorption (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Malabsorption syndrome\Congenital monosaccharide malabsorption\Congenital glucose-galactose malabsorption
• \Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Malabsorption syndrome\Congenital monosaccharide malabsorption\Congenital glucose-galactose malabsorption
• \Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Malabsorption syndrome\Congenital monosaccharide malabsorption\Congenital glucose-galactose malabsorption
• \Disease\Metabolic disease\Disorder of carbohydrate metabolism\Disorder of carbohydrate absorption\Congenital monosaccharide malabsorption\Congenital glucose-galactose malabsorption
• \Disease\Metabolic disease\Disorder of carbohydrate metabolism\Disorder of carbohydrate transport\Congenital glucose-galactose malabsorption
• \Disease\Congenital disease\Congenital monosaccharide malabsorption\Congenital glucose-galactose malabsorption

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
46787015	Congenital glucose-galactose malabsorption	en	Synonym	Active	Case insensitive	SNOMED CT core
46788013	Congenital glucose-galactose intolerance	en	Synonym	Active	Case insensitive	SNOMED CT core
758568015	Congenital glucose-galactose malabsorption (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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