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1187194006: 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
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
3408191001000115 Enteropathie, chronische, SLCO2A1-Gen-assoziierte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5789681000241112 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) SNOMED CT Switzerland NRC maintained Module
5789691000241114 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) SNOMED CT Switzerland NRC maintained Module
5789681000241112 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) SNOMED CT Switzerland NRC maintained Module
5789691000241114 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) SNOMED CT Switzerland NRC maintained Module
3408191001000115 Enteropathie, chronische, SLCO2A1-Gen-assoziierte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

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 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) Is a Ulceration of small intestine true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) Clinical course Chronic persistent true Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 1
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene (disorder) Associated morphology Multiple ulcers true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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