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 |
| 351207014 | Blood group deletion syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 622726012 | Blood group deletion syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1495080011 | McLeod syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Blood group deletion syndrome | Is a | Erythrocyte membrane abnormality | true | Inferred relationship | Existential restriction modifier | ||
| Blood group deletion syndrome | Finding site | Hematopoietic system structure | false | Inferred relationship | Existential restriction modifier | ||
| Blood group deletion syndrome | Finding site | Erythrocyte | true | Inferred relationship | Existential restriction modifier | 1 | |
| Blood group deletion syndrome | Finding site | Hematopoietic system structure | false | Inferred relationship | Existential restriction modifier | ||
| Blood group deletion syndrome | Has definitional manifestation | Red blood cell finding | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR