Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 180441019 | Inherited weak D phenotype | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 671695014 | Inherited weak D phenotype (finding) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited weak D phenotype | Finding site | Haematopoietic system structure | false | Inferred relationship | Some | ||
| Inherited weak D phenotype | Interprets | Laboratory test | false | Inferred relationship | Some | ||
| Inherited weak D phenotype | Finding method | Procedure | false | Inferred relationship | Some | ||
| Inherited weak D phenotype | Interprets | Genetic test | true | Inferred relationship | Some | 2 | |
| Inherited weak D phenotype | Interprets | Blood transfusion test | true | Inferred relationship | Some | 1 | |
| Inherited weak D phenotype | Is a | Weak D phenotype | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR