Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3450391016 | Intestinal-type adenoma (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3450392011 | Intestinal-type adenoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4839661000146119 | intestinaal type adenoom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 4839671000146113 | intestinaal type adenoom (afwijkende morfologie) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Intestinal-type adenoma (morphologic abnormality) | Is a | benigne adenomateus neoplasma - categorie (afwijkende morfologie) | false | Inferred relationship | Some | ||
| Intestinal-type adenoma (morphologic abnormality) | Is a | Benign adenomatous neoplasm (morphologic abnormality) | false | Inferred relationship | Some | ||
| Intestinal-type adenoma (morphologic abnormality) | Is a | Adenoma (morphologic abnormality) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Intestinal-type adenoma of ampulla of Vater (disorder) | Associated morphology | True | Intestinal-type adenoma (morphologic abnormality) | Inferred relationship | Some | 1 |
| Benign intestinal-type adenoma of stomach (disorder) | Associated morphology | True | Intestinal-type adenoma (morphologic abnormality) | Inferred relationship | Some | 1 |
This concept is not in any reference sets
FHIR