Status: current, Defined. Date: 31-Jan 2005. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2534454017 | Refractory cytopenia with multilineage dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
2534455016 | Refractory cytopaenia with multilineage dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
4953726015 | Myelodysplastic syndrome with multilineage dysplasia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4953727012 | Myelodysplastic syndrome with multilineage dysplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Refractory cytopaenia with multilineage dysplasia | Is a | Myelodysplastic syndrome | true | Inferred relationship | Some | ||
Refractory cytopaenia with multilineage dysplasia | Is a | Primary malignant neoplasm of bone marrow | false | Inferred relationship | Some | ||
Refractory cytopaenia with multilineage dysplasia | Finding site | Bone marrow structure | false | Inferred relationship | Some | 1 | |
Refractory cytopaenia with multilineage dysplasia | Associated morphology | Refractory cytopenia with multilineage dysplasia | false | Inferred relationship | Some | 1 | |
Refractory cytopaenia with multilineage dysplasia | Associated morphology | Refractory cytopenia with multilineage dysplasia | true | Inferred relationship | Some | 1 | |
Refractory cytopaenia with multilineage dysplasia | Finding site | Bone marrow structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome | Is a | True | Refractory cytopaenia with multilineage dysplasia | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set