28212002: Intestinal lipofuscinosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Bowel finding\Disorder of intestine\Intestinal lipofuscinosis

\Digestive system finding\Gastrointestinal tract finding\Bowel finding\Disorder of intestine\Intestinal lipofuscinosis
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal lipofuscinosis
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Intestinal lipofuscinosis
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal lipofuscinosis
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of intestine\Intestinal lipofuscinosis

\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 lipofuscinosis
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Intestinal lipofuscinosis
\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 lipofuscinosis
\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 lipofuscinosis

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipofuscinosis\Intestinal lipofuscinosis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Intestinal lipofuscinosis
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Intestinal lipofuscinosis
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Intestinal lipofuscinosis
\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 lipofuscinosis
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of intestine\Intestinal lipofuscinosis
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Disorder of intestine\Intestinal lipofuscinosis
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipofuscinosis\Intestinal lipofuscinosis
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Lipofuscinosis\Intestinal lipofuscinosis
\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Lipofuscinosis\Intestinal lipofuscinosis
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Lipofuscinosis\Intestinal lipofuscinosis

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

47224015 Intestinal lipofuscinosis en Synonym Active Entire term case insensitive SNOMED CT core module

47225019 Brown bowel syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

758867018 Intestinal lipofuscinosis (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
Intestinal lipofuscinosis	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier
Intestinal lipofuscinosis	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Intestinal lipofuscinosis	Is a	Disorder of intestine	true	Inferred relationship	Existential restriction modifier
Intestinal lipofuscinosis	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Intestinal lipofuscinosis	Is a	Lipofuscinosis	true	Inferred relationship	Existential restriction modifier
Intestinal lipofuscinosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Intestinal lipofuscinosis	Finding site	Intestinal structure	true	Inferred relationship	Existential restriction modifier	2

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
47224015	Intestinal lipofuscinosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
47225019	Brown bowel syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
758867018	Intestinal lipofuscinosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module