Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3776724019 | Hereditary acroosteolysis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3776725018 | Hereditary acroosteolysis | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Acroosteolysis, keloid-like lesions, premature ageing syndrome | Is a | True | Hereditary acroosteolysis | Inferred relationship | Some | |
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome | Is a | True | Hereditary acroosteolysis | Inferred relationship | Some | |
Giacci familial neurogenic acroosteolysis | Is a | True | Hereditary acroosteolysis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set