Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3944205013 | Hyperphosphataemic familial tumoural calcinosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3944206014 | Hyperphosphatemic familial tumoral calcinosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3944207017 | Hyperphosphatemic familial tumoral calcinosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hyperphosphataemic familial tumoural calcinosis | Is a | Tumoural calcinosis | true | Inferred relationship | Some | ||
Hyperphosphataemic familial tumoural calcinosis | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Hyperphosphataemic familial tumoural calcinosis | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Hyperphosphataemic familial tumoural calcinosis | Associated morphology | Dystrophic calcification | true | Inferred relationship | Some | 1 | |
Hyperphosphataemic familial tumoural calcinosis | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Hyperphosphataemic familial tumoural calcinosis | Associated morphology | Pathologic calcification | false | Inferred relationship | Some | 2 | |
Hyperphosphataemic familial tumoural calcinosis | Finding site | Subcutaneous tissue structure | false | Inferred relationship | Some | 2 | |
Hyperphosphataemic familial tumoural calcinosis | Finding site | Structure of joint region | true | Inferred relationship | Some | 2 | |
Hyperphosphataemic familial tumoural calcinosis | Associated morphology | Dystrophic calcification | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set