78960005: Pancreatic triacylglycerol lipase deficiency (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Finding of pancreas\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency

\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Malabsorption syndrome\Pancreatic triacylglycerol lipase deficiency
\Digestive system finding\Finding of pancreas\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Malabsorption syndrome\Pancreatic triacylglycerol lipase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Finding of pancreas\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Pancreatic triacylglycerol lipase deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Pancreatic triacylglycerol lipase deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Malabsorption syndrome\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of pancreas\Pancreatic triacylglycerol lipase deficiency
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Pancreatic triacylglycerol lipase deficiency
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Pancreatic triacylglycerol lipase deficiency
\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Pancreatic triacylglycerol lipase deficiency
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Pancreatic triacylglycerol lipase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

131020011 Pancreatic triacylglycerol lipase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

131021010 Isolated lipase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

131022015 Congenital absence of pancreatic lipase en Synonym Active Entire term case insensitive SNOMED CT core module

503970014 Congenital pancreatic lipase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

503971013 Congenital deficiency of pancreatic lipase en Synonym Active Entire term case insensitive SNOMED CT core module

819957015 Pancreatic triacylglycerol lipase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pancreatic triacylglycerol lipase deficiency	Is a	Disorder of lipid storage and metabolism	true	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Disorder of pancreas	true	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Disorder of lysosomal enzyme	true	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Malabsorption syndrome	true	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Finding site	Structure of small intestine	false	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Pancreatic triacylglycerol lipase deficiency	Finding site	Pancreatic structure	true	Inferred relationship	Existential restriction modifier	2
Pancreatic triacylglycerol lipase deficiency	Finding site	Gastrointestinal tract structure	true	Inferred relationship	Existential restriction modifier	3
Pancreatic triacylglycerol lipase deficiency	Is a	Finding of pancreas	false	Inferred relationship	Existential restriction modifier
Pancreatic triacylglycerol lipase deficiency	Is a	Hereditary disorder of endocrine system	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
131020011	Pancreatic triacylglycerol lipase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
131021010	Isolated lipase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
131022015	Congenital absence of pancreatic lipase	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
503970014	Congenital pancreatic lipase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
503971013	Congenital deficiency of pancreatic lipase	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
819957015	Pancreatic triacylglycerol lipase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module