Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 207429012 | Refractory cytopenia with multilineage dysplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3009266015 | Refractory cytopenia of childhood | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4953715014 | Myelodysplastic syndrome with multilineage dysplasia (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4953716010 | Myelodysplastic syndrome with multilineage dysplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Myelodysplastic syndrome with multilineage dysplasia | Is a | Malignant neoplasm, primary | false | Inferred relationship | Existential restriction modifier | ||
| Myelodysplastic syndrome with multilineage dysplasia | Is a | Myelodysplastic syndrome | false | Inferred relationship | Existential restriction modifier | ||
| Myelodysplastic syndrome with multilineage dysplasia | Is a | Myelodysplastic syndrome | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Refractory cytopenia with multilineage dysplasia and ringed sideroblasts | Is a | False | Myelodysplastic syndrome with multilineage dysplasia | Inferred relationship | Existential restriction modifier | |
| Myelodysplastic syndrome with multilineage dysplasia | Associated morphology | False | Myelodysplastic syndrome with multilineage dysplasia | Inferred relationship | Existential restriction modifier | 1 |
| Myelodysplastic syndrome with multilineage dysplasia | Associated morphology | True | Myelodysplastic syndrome with multilineage dysplasia | Inferred relationship | Existential restriction modifier | 1 |
| Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome | Associated morphology | True | Myelodysplastic syndrome with multilineage dysplasia | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets
FHIR