56661000: Intestinal enteropeptidase deficiency (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Bowel finding\Disorder of intestine\Intestinal enteropeptidase deficiency

\Digestive system finding\Gastrointestinal tract finding\Bowel finding\Disorder of intestine\Intestinal enteropeptidase deficiency
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Malabsorption syndrome\Intestinal enteropeptidase deficiency
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Gastrointestinal complication\Intestinal enteropeptidase deficiency
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Intestinal enteropeptidase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Malabsorption syndrome\Intestinal enteropeptidase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Gastrointestinal complication\Intestinal enteropeptidase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of intestine\Intestinal enteropeptidase deficiency

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Intestinal enteropeptidase deficiency
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Intestinal enteropeptidase deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Intestinal enteropeptidase deficiency
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Intestinal enteropeptidase deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Intestinal enteropeptidase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Intestinal enteropeptidase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Malabsorption syndrome\Intestinal enteropeptidase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Gastrointestinal complication\Intestinal enteropeptidase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of intestine\Intestinal enteropeptidase deficiency
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal enteropeptidase deficiency
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Intestinal enteropeptidase deficiency
\Disease\Metabolic disease\Enzymopathy\Intestinal enteropeptidase deficiency
\Disease\Congenital disease\Inborn error of metabolism\Intestinal enteropeptidase 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

94228011 Intestinal enteropeptidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

94229015 Intestinal enterokinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

94230013 Intestinal pseudo-trypsinogen deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

795198010 Intestinal enteropeptidase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

5150934016 Congenital enterokinase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

5150935015 Congenital enteropathy due to enteropeptidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Intestinal enteropeptidase deficiency	Is a	Inborn error of metabolism	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Enzymopathy	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Malabsorption syndrome	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Intestinal enteropeptidase deficiency	Finding site	Structure of small intestine	false	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Is a	Disorder of intestine	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Finding site	Intestinal structure	true	Inferred relationship	Existential restriction modifier	2
Intestinal enteropeptidase deficiency	Is a	Gastrointestinal complication	true	Inferred relationship	Existential restriction modifier
Intestinal enteropeptidase deficiency	Due to	Deficiency of enteropeptidase	true	Inferred relationship	Existential restriction modifier	3

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
94228011	Intestinal enteropeptidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
94229015	Intestinal enterokinase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
94230013	Intestinal pseudo-trypsinogen deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
795198010	Intestinal enteropeptidase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
5150934016	Congenital enterokinase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5150935015	Congenital enteropathy due to enteropeptidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module