Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | Reference Sets |
| 89950015 | Congenital pancreatic trypsin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | Lateralizable body structure reference set (foundation metadata concept) |
| 792315014 | Congenital pancreatic trypsin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | GB English: Preferred (foundation metadata concept) |
| 747441000052118 | medfödd brist på pankreatiskt trypsin | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital pancreatic trypsin deficiency (disorder) | Is a | kongenital anomali i pankreas | false | Inferred relationship | Some | ||
| Congenital pancreatic trypsin deficiency (disorder) | Finding site | Pancreatic structure | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Congenital pancreatic trypsin deficiency (disorder) | Associated morphology | Developmental anomaly (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Associated morphology | medfödd brist | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Finding site | Digestive organ structure | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Is a | Deficiency of trypsin | true | Inferred relationship | Some | ||
| Congenital pancreatic trypsin deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Finding site | Digestive organ structure | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | 2 | |
| Congenital pancreatic trypsin deficiency (disorder) | Associated morphology | medfödd brist | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Finding site | Pancreatic structure | false | Inferred relationship | Some | 1 | |
| Congenital pancreatic trypsin deficiency (disorder) | Finding site | Digestive organ structure | false | Inferred relationship | Some | 2 | |
| Congenital pancreatic trypsin deficiency (disorder) | Finding site | Pancreatic structure | false | Inferred relationship | Some | 2 | |
| Congenital pancreatic trypsin deficiency (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | 2 | |
| Congenital pancreatic trypsin deficiency (disorder) | Is a | Congenital disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR