69478001: Pancreatic colipase deficiency (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\...

\Finding of pancreas\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency

\Bowel finding\Finding of small intestine (finding)\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Bowel finding\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency

\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Finding of small intestine (finding)\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Finding of pancreas\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Pancreatic colipase deficiency
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Pancreatic colipase deficiency

\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 malabsorption\Pancreatic colipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Finding of pancreas\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Finding of small intestine (finding)\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\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 malabsorption\Pancreatic colipase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\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 malabsorption\Pancreatic colipase deficiency
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Pancreatic colipase deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pancreatic colipase deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Pancreatic colipase deficiency
\Disease\Disorder of foetus and/or newborn\Congenital disease\Inborn error of metabolism\Pancreatic colipase deficiency
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Pancreatic colipase deficiency
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of endocrine system (disorder)\Pancreatic colipase deficiency
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Hereditary disorder of endocrine system (disorder)\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Pancreatic colipase deficiency
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of retroperitoneal compartment (disorder)\Disease of pancreas\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Disorder of small intestine (disorder)\Pancreatic malabsorption\Pancreatic colipase deficiency
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Pancreatic colipase deficiency
\Disease\Metabolic disease\Enzymopathy\Pancreatic colipase deficiency

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 colipase deficiency	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Malabsorption syndrome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Enzymopathy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Disease of pancreas	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Disorder of lipid storage and metabolism	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Pancreatic colipase deficiency	Finding site	Structure of small intestine (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Finding site	Pancreatic structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Is a	Pancreatic malabsorption	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Congenital anomaly of pancreas	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Finding site	Structure of digestive system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Finding site	Digestive organ structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Congenital anomaly of digestive tract	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Is a	Congenital anomaly of small intestine	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	Finding site	Structure of small intestine (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Finding site	Pancreatic structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Finding site	Pancreatic structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Pancreatic colipase deficiency	Finding site	Structure of small intestine (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic colipase deficiency	Is a	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Pancreatic colipase deficiency	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
115426011	Pancreatic colipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
809427011	Pancreatic colipase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
115426011	Pancreatic colipase deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
115426011	Pancreatic colipase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
809427011	Pancreatic colipase deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
809427011	Pancreatic colipase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3432851001000111	Colipase-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
942041000172114	déficit en colipase pancréatique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
942041000172114	déficit en colipase pancréatique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3432851001000111	Colipase-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module