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 |
| 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
FHIR