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 |
3793710015 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3793711016 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3793712011 | Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3793714012 | Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3793721012 | HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3793726019 | HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3793727011 | HPFH (hereditary persistence of foetal haemoglobin) delta beta plus thalassaemia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets