78960005: Pancreatic triacylglycerol lipase deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Abdominal organ finding\Finding of pancreas\Disease of pancreas\Pancreatic triacylglycerol lipase deficiency (disorder)

\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Pancreatic triacylglycerol lipase deficiency (disorder)
\Digestive system finding (finding)\Finding of pancreas\Disease of pancreas\Pancreatic triacylglycerol lipase deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Pancreatic triacylglycerol lipase deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of pancreas\Pancreatic triacylglycerol lipase deficiency (disorder)
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Pancreatic triacylglycerol lipase deficiency (disorder)

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Disorder of lysosomal enzyme\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Hereditary disorder of endocrine system (disorder)\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disease of pancreas\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of pancreas\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of retroperitoneal compartment (disorder)\Disease of pancreas\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Pancreatic triacylglycerol lipase deficiency (disorder)
\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Pancreatic triacylglycerol lipase deficiency (disorder)

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

Descriptions:

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
131020011	Pancreatic triacylglycerol lipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
131021010	Isolated lipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
131022015	Congenital absence of pancreatic lipase	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
503970014	Congenital pancreatic lipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
503971013	Congenital deficiency of pancreatic lipase	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
819957015	Pancreatic triacylglycerol lipase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
131020011	Pancreatic triacylglycerol lipase deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
131020011	Pancreatic triacylglycerol lipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
131021010	Isolated lipase deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
131021010	Isolated lipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
131022015	Congenital absence of pancreatic lipase	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
131022015	Congenital absence of pancreatic lipase	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
503970014	Congenital pancreatic lipase deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
503970014	Congenital pancreatic lipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
503971013	Congenital deficiency of pancreatic lipase	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
503971013	Congenital deficiency of pancreatic lipase	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
819957015	Pancreatic triacylglycerol lipase deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
819957015	Pancreatic triacylglycerol lipase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3422811001000112	Triglycerid-Lipase-Mangel, pankreatischer	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
926751000172112	déficit en triacylglycérol lipase pancréatique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
979601000172113	déficit en triglycéride lipase pancréatique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
926751000172112	déficit en triacylglycérol lipase pancréatique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
979601000172113	déficit en triglycéride lipase pancréatique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3422811001000112	Triglycerid-Lipase-Mangel, pankreatischer	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module