Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5048456018 | Primary desmosis coli (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5048457010 | Primary desmosis coli | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048458017 | Aplastic desmosis coli | en | Synonym | Active | Case insensitive | SNOMED CT core |
5048459013 | A rare intestinal disease with characteristics of congenital partial or complete lack of the collagen mesh network in the intestinal wall resulting in hypoperistalsis or aperistalsis. The enteric nervous system is normal or near normal in the affected areas, although hypo and dysganglionosis may be found in some proximal segments of the colon and/or small bowel. Patients present with chronic intractable slow transit constipation. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary desmosis coli | Is a | Congenital anomaly of intestinal tract | true | Inferred relationship | Some | ||
Primary desmosis coli | Is a | Functional disorder of intestine | true | Inferred relationship | Some | ||
Primary desmosis coli | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Primary desmosis coli | Finding site | Intestinal wall structure | true | Inferred relationship | Some | 1 | |
Primary desmosis coli | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
Primary desmosis coli | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set