Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2731067011 | Congenital hemihypertrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 315645014 | Congenital hemihypertrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hemihypertrophy | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital hemihypertrophy | Associated morphology | Hypertrophy | true | Inferred relationship | Some | 1 | |
| Congenital hemihypertrophy | Is a | Finding of body region | false | Inferred relationship | Some | ||
| Congenital hemihypertrophy | Is a | Disorder by body site | false | Inferred relationship | Some | ||
| Congenital hemihypertrophy | Finding site | Structure of half of body lateral to midsagittal plane | true | Inferred relationship | Some | 1 | |
| Congenital hemihypertrophy | Is a | Congenital anomaly | true | Inferred relationship | Some | ||
| Congenital hemihypertrophy | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital hemihypertrophy | Associated morphology | Congenital hemihypertrophy | 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