Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5401029018 | Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401030011 | Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhoea that leads to irreversible intestinal failure. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3303361018 | Congenital tufting enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303363015 | Tufting enteropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303364014 | Congenital epithelial dysplasia of intestine (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303365010 | Congenital epithelial dysplasia of intestine | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303366011 | Intestinal epithelial dysplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Disorder of duodenum | false | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Congenital disease | false | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Disorder of gastrointestinal tract mucous membrane (disorder) | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Lesion of soft tissue (disorder) | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Lesion of mucosa (disorder) | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Disorder of soft tissue of trunk | false | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Disorder of jejunum | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Associated morphology | Epithelial dysplasia | true | Inferred relationship | Some | 2 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Finding site | Jejunal mucous membrane structure | true | Inferred relationship | Some | 2 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Associated morphology | Epithelial dysplasia | false | Inferred relationship | Some | 3 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Finding site | Duodenal mucous membrane structure | false | Inferred relationship | Some | 3 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Congenital anomaly of duodenum | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Finding site | Duodenal mucous membrane structure | true | Inferred relationship | Some | 1 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Associated morphology | Epithelial dysplasia | true | Inferred relationship | Some | 1 | |
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Congenital anomaly of lower alimentary tract | true | Inferred relationship | Some | ||
| Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure. | Is a | Disorder of soft tissue of abdominal cavity | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR