Thalassemia: An inherited blood disorder characterized by a decreased synthesis of one of the polypeptide chains that form hemoglobin. Anemia results from this abnormal hemoglobin formation.
| Name | D3_THALASSAEMIA |
|---|---|
| Long name | Thalassaemia |
| Hospital Discharge registry | ICD-10: D56 |
| Cause of Death registry | ICD-10: D56 |
| Include | D3_ALPHATHALASSAEMIA, D3_BETATHALASSAEMIA, D3_DELTABETATHALASSAEMIA, D3_THALASSAEMIATRAIT, D3_HPFH, D3_THALASSAEMIANAS |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
| Latin name | Thalassaemia |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 21 | 9 | 12 |
| Unadjusted prevalence (%) | 0.01 | 0.01 | 0.01 |
| Mean age at first event (years) | 49.24 | 43.69 | 53.40 |
| Case fatality at 5-years (%) | 0.00 | 0.00 | 0.00 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 1.0 | 1.0 | 1.0 |
| Recurrence at 6 months (%) | 9.52 | 11.11 | 8.33 |
before Thalassaemia
after Thalassaemia
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