Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 48666014 | Meckel-Gruber syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 48667017 | Dysencephalia splanchnocystica | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 759929010 | Meckel-Gruber syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Meckel-Gruber syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Meckel-Gruber syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Meckel-Gruber syndrome | Is a | Multiple malformation syndrome with unusual brain and/or neuromuscular findings | true | Inferred relationship | Some | ||
| Meckel-Gruber syndrome | Associated morphology | Congenital malformation | false | Inferred relationship | Some | ||
| Meckel-Gruber syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Meckel-Gruber syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Meckel-Gruber syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Meckel-Gruber syndrome | Finding site | Brain structure | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR