Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1220945019 | Atrophic | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 22797016 | Atrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 737978016 | Atrophy (morphologic abnormality) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Atrophy | Is a | Degenerative abnormality | false | Inferred relationship | Some | ||
| Atrophy | Is a | Degeneration | false | Inferred relationship | Some | ||
| Atrophy | Is a | Degenerative abnormality | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Combined immunodeficiency with faciooculoskeletal anomalies syndrome | Associated morphology | True | Atrophy | Inferred relationship | Some | 1 |
| Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly | Associated morphology | True | Atrophy | Inferred relationship | Some | 2 |
| Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly | Associated morphology | False | Atrophy | Inferred relationship | Some | 3 |
| Autosomal dominant neovascular inflammatory vitreoretinopathy | Associated morphology | True | Atrophy | Inferred relationship | Some | 2 |
| Charcot-Marie-Tooth disease type 2B5 | Associated morphology | True | Atrophy | Inferred relationship | Some | 1 |
| Atrophic spots of skin | Associated morphology | False | Atrophy | Inferred relationship | Some | 1 |
Reference Sets
Body structure foundation reference set
FHIR