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

SNOMED CT Concept\Clinical finding\...

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

\Finding of small intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene

\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene

\Digestive system finding\Gastrointestinal tract finding\Bowel finding\Finding of small intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Gastrointestinal tract finding\Bowel finding\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Gastrointestinal tract finding\Bowel finding\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Gastrointestinal tract finding\Disorder of gastrointestinal tract\Gastrointestinal ulcer\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Chronic digestive system disorder\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Gastrointestinal ulcer\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Bowel finding\Finding of small intestine\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Bowel finding\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Bowel finding\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Ulcer\Gastrointestinal ulcer\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Chronic digestive system disorder\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of gastrointestinal tract\Gastrointestinal ulcer\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Disorder of small intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of lower gastrointestinal tract\Intestinal disease\Ulceration of intestine\Ulceration of small intestine\Chronic enteropathy associated with SLCO2A1 gene
\Disease\Chronic disease\Chronic digestive system disorder\Chronic enteropathy associated with SLCO2A1 gene

Status: current, Primitive. 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 Active Initial character case insensitive SNOMED CT core

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

4670332013 Chronic enteropathy associated with SLCO2A1 gene en Synonym Active Initial character case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chronic enteropathy associated with SLCO2A1 gene	Is a	Chronic digestive system disorder	true	Inferred relationship	Some
Chronic enteropathy associated with SLCO2A1 gene	Is a	Ulceration of small intestine	true	Inferred relationship	Some
Chronic enteropathy associated with SLCO2A1 gene	Is a	Digestive system hereditary disorder	true	Inferred relationship	Some
Chronic enteropathy associated with SLCO2A1 gene	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Chronic enteropathy associated with SLCO2A1 gene	Clinical course	Chronic persistent	true	Inferred relationship	Some	2
Chronic enteropathy associated with SLCO2A1 gene	Finding site	Structure of small intestine	true	Inferred relationship	Some	1
Chronic enteropathy associated with SLCO2A1 gene	Associated morphology	Multiple ulcers	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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	Active	Initial character case insensitive	SNOMED CT core
4670331018	Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
4670332013	Chronic enteropathy associated with SLCO2A1 gene	en	Synonym	Active	Initial character case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core