1187194006: Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)

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

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

\Finding of small intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)

\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)

\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Finding of small intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Gastrointestinal ulcer (disorder)\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Chronic digestive system disorder\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Gastrointestinal ulcer (disorder)\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Finding of small intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Ulcer (disorder)\Gastrointestinal ulcer (disorder)\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Chronic digestive system disorder\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Gastrointestinal ulcer (disorder)\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive organ (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of lower gastrointestinal tract (disorder)\Disorder of intestine\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)
\Disease\Chronic disease\Chronic digestive system disorder\Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4670330017 Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4670331018 Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4670332013 Chronic enteropathy associated with SLCO2A1 gene en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

4670328019 A rare genetic gastroenterological disease characterised by the presence of multiple persistent, intractable ulcers of the small intestine, leading to chronic blood and protein loss. Signs and symptoms include abdominal pain, anaemia, fatigue, oedema, and diarrhoea. Morphologically, the condition manifests with multiple sharply demarcated shallow lesions with irregular circular or linear shape. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4670329010 A rare genetic gastroenterological disease characterized by the presence of multiple persistent, intractable ulcers of the small intestine, leading to chronic blood and protein loss. Signs and symptoms include abdominal pain, anemia, fatigue, edema, and diarrhea. Morphologically, the condition manifests with multiple sharply demarcated shallow lesions with irregular circular or linear shape. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

10027721000172118 entéropathie chronique associée au gène des transporteurs d'anions organiques porteur de soluté de la famille 2A1 fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

10027731000172115 entéropathie chronique associée au gène SLCO2A1 (solute carrier organic anion transporter family member 2A1) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

7210881000172119 chronische enteropathie door mutatie in 'solute carrier organic anion transporter family member 2A1'-gen nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

7210891000172116 chronische enteropathie door mutatie in SLCO2A1-gen nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

7210901000172117 chronische darmaandoening door SLCO2A1-mutatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Is a	Chronic digestive system disorder	true	Inferred relationship	Some
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Is a	Ulceration of small intestine	true	Inferred relationship	Some
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Is a	Digestive system hereditary disorder (disorder)	true	Inferred relationship	Some
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Clinical course	Chronic persistent	true	Inferred relationship	Some	2
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Finding site	Structure of small intestine (body structure)	true	Inferred relationship	Some	1
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	Associated morphology	Multiple ulcers (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
4670330017	Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4670331018	Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4670332013	Chronic enteropathy associated with SLCO2A1 gene	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4670328019	A rare genetic gastroenterological disease characterised by the presence of multiple persistent, intractable ulcers of the small intestine, leading to chronic blood and protein loss. Signs and symptoms include abdominal pain, anaemia, fatigue, oedema, and diarrhoea. Morphologically, the condition manifests with multiple sharply demarcated shallow lesions with irregular circular or linear shape.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4670329010	A rare genetic gastroenterological disease characterized by the presence of multiple persistent, intractable ulcers of the small intestine, leading to chronic blood and protein loss. Signs and symptoms include abdominal pain, anemia, fatigue, edema, and diarrhea. Morphologically, the condition manifests with multiple sharply demarcated shallow lesions with irregular circular or linear shape.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
10027721000172118	entéropathie chronique associée au gène des transporteurs d'anions organiques porteur de soluté de la famille 2A1	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
10027731000172115	entéropathie chronique associée au gène SLCO2A1 (solute carrier organic anion transporter family member 2A1)	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
7210881000172119	chronische enteropathie door mutatie in 'solute carrier organic anion transporter family member 2A1'-gen	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
7210891000172116	chronische enteropathie door mutatie in SLCO2A1-gen	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
7210901000172117	chronische darmaandoening door SLCO2A1-mutatie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)