Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 15445015 | Hecht syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 15446019 | Trismus pseudocamptodactyly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 830072015 | Hecht syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hecht syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 | |
| Hecht syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Hecht syndrome | Associated morphology | Congenital malformation | false | Inferred relationship | Some | ||
| Hecht syndrome | Is a | Multiple malformation syndrome with unusual brain and/or neuromuscular findings | true | Inferred relationship | Some | ||
| Hecht syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hecht syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Hecht syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Hecht 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