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 |
3793694018 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3793695017 | Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3793698015 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3800043011 | HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3800044017 | HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3800045016 | HPFH (hereditary persistence of foetal haemoglobin) G gamma 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