763212006: Combined pancreatic lipase and colipase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Metabolic disease\Metabolic disorder of transport\Combined pancreatic lipase and colipase deficiency
• \Metabolic disease\Enzymopathy\Combined pancreatic lipase and colipase deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipid metabolism disorder\Combined pancreatic lipase and colipase deficiency
• \Congenital disease\Combined pancreatic lipase and colipase deficiency

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3638182011	Combined pancreatic lipase and colipase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3638183018	Combined pancreatic lipase and colipase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3638184012	A disorder of lipid absorption and transport characterized by steatorrhea with foul-smelling stools from birth, diminished serum carotene and vitamin E and a combined deficiency of the pancreatic enzymes lipase and colipase. Patients are otherwise healthy and develop normally with no apparent pancreatic disease. There have been no further descriptions in the literature since 1990.	en	Definition	Active	Case sensitive	SNOMED CT core
3638185013	A disorder of lipid absorption and transport characterised by steatorrhoea with foul-smelling stools from birth, diminished serum carotene and vitamin E and a combined deficiency of the pancreatic enzymes lipase and colipase. Patients are otherwise healthy and develop normally with no apparent pancreatic disease. There have been no further descriptions in the literature since 1990.	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

Description inactivation indicator reference set

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