197260007: Intestinal lymphangiectasis (disorder)

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

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Intestinal lymphangiectasis
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Intestinal lymphangiectasis

\General finding of soft tissue\Disorder of soft tissue\...

\Lesion of soft tissue (disorder)\Intestinal lymphangiectasis

\Disorder of lymphatic vessel (disorder)\Intestinal lymphangiectasis

\Disease\Disorder of body system\Disorder of lymphatic system\Disorder of lymphatic vessel (disorder)\Intestinal lymphangiectasis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Intestinal lymphangiectasis
\Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Intestinal lymphangiectasis
\Disease\Disorder of soft tissue\Disorder of lymphatic vessel (disorder)\Intestinal lymphangiectasis

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

303366015 Intestinal lymphangiectasis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

303367012 Intestinal lymphangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

581613013 Intestinal lymphangiectasis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1004761000172117 lymphangiectasie intestinale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3439051001000110 Lymphangiektasie, intestinale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Intestinal lymphangiectasis	Is a	Disorder of small intestine	false	Inferred relationship	Some
Intestinal lymphangiectasis	Is a	Disorder of lymphatic vessel (disorder)	true	Inferred relationship	Some
Intestinal lymphangiectasis	Finding site	Structure of small intestine (body structure)	false	Inferred relationship	Some
Intestinal lymphangiectasis	Finding site	Structure of lymphatic vessel	false	Inferred relationship	Some
Intestinal lymphangiectasis	Associated morphology	Lymphangiectasis	false	Inferred relationship	Some	1
Intestinal lymphangiectasis	Is a	Disorder of intestine	false	Inferred relationship	Some
Intestinal lymphangiectasis	Finding site	Intestinal structure	false	Inferred relationship	Some	1
Intestinal lymphangiectasis	Is a	Disorder of abdomen (disorder)	false	Inferred relationship	Some
Intestinal lymphangiectasis	Finding site	Structure of lymphatic vessel of intestine (body structure)	false	Inferred relationship	Some	1
Intestinal lymphangiectasis	Is a	Lesion of soft tissue (disorder)	true	Inferred relationship	Some
Intestinal lymphangiectasis	Finding site	Structure of lymphatic vessel of intestine (body structure)	true	Inferred relationship	Some	1
Intestinal lymphangiectasis	Associated morphology	Lymphangiectasis	true	Inferred relationship	Some	1
Intestinal lymphangiectasis	Is a	Disorder of abdominopelvic segment of trunk	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Primary lymphangiectasis of intestine (disorder)	Is a	True	Intestinal lymphangiectasis	Inferred relationship	Some
Secondary intestinal lymphangiectasia	Is a	False	Intestinal lymphangiectasis	Inferred relationship	Some
Secondary intestinal lymphangiectasia is an acquired from of intestinal lymphangiectasia manifesting as a protein-losing enteropathy due to another disorder such as Crohn's disease, congestive heart failure, sarcoidosis, Turner syndrome and often in patients who have undergone a Fontan operation. It is characterised by malabsorption, diarrhoea, oedema due hypoproteinaemia, steatorrhoea and serosal effusions.	Is a	True	Intestinal lymphangiectasis	Inferred relationship	Some
An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985.	Is a	True	Intestinal lymphangiectasis	Inferred relationship	Some
Hennekam lymphangiectasia-lymphedema syndrome (disorder)	Is a	True	Intestinal lymphangiectasis	Inferred relationship	Some

This concept is not in any reference sets