Status: current, 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 |
| 3446352013 | Congenital duplication of rectum (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3446353015 | Congenital duplication of rectum | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3446354014 | Rectal duplication | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3446355010 | A rare congenital anorectal malformation with characteristics of an egg-like, cystic, mucus-filled mass, composed of intestinal mucosal lining and smooth muscle tissue. Commonly they present in childhood with symptoms of recurrent urinary tract infections, gastroenteritis, obstruction, perianal sepsis and rectal bleeding. Drainage of mucus or pus from the anus is also a typical presenting sign. The majority of malformations are found in the retro-rectal space where they communicate with or are contiguous to the rectum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5488801000241119 | duplication congénitale du rectum | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital duplication of rectum (disorder) | Is a | Congenital duplication of intestine | true | Inferred relationship | Some | ||
| Congenital duplication of rectum (disorder) | Is a | Congenital anomaly of rectum | true | Inferred relationship | Some | ||
| Congenital duplication of rectum (disorder) | Associated morphology | Double structure | true | Inferred relationship | Some | 1 | |
| Congenital duplication of rectum (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital duplication of rectum (disorder) | Finding site | Rectum structure | true | Inferred relationship | Some | 1 | |
| Congenital duplication of rectum (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR