Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2007. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2662307010 | Hereditary hemoglobinopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2674112019 | Hereditary hemoglobinopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
2674113012 | Hereditary haemoglobinopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Homozygous hemoglobinopathy | Is a | True | Hereditary hemoglobinopathy | Inferred relationship | Existential restriction modifier | |
Thalassemia | Is a | True | Hereditary hemoglobinopathy | Inferred relationship | Existential restriction modifier | |
Hereditary hemoglobinopathy due to globin chain mutation | Is a | True | Hereditary hemoglobinopathy | Inferred relationship | Existential restriction modifier | |
Hereditary persistence of fetal hemoglobin | Is a | True | Hereditary hemoglobinopathy | Inferred relationship | Existential restriction modifier | |
Heterozygous hemoglobinopathy | Is a | True | Hereditary hemoglobinopathy | Inferred relationship | Existential restriction modifier | |
Hemoglobinopathy Toms River | Is a | True | Hereditary hemoglobinopathy | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets