hereditary hemochromatosis type 1: Hemochromatosis type 1 (classic) is the most common form of hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition. Due to its incidence (1/200-1/1000), it is not considered as a rare disease, unlike the other subforms of the disease
| Name | E4_IRON_MET |
|---|---|
| Long name | Disorders of iron metabolism |
| Hospital Discharge registry | ICD-10: E831 |
| Cause of Death registry | ICD-10: E831 |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
| Latin name | Perturbationes metabolismi ferri |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 146 | 60 | 86 |
| Unadjusted prevalence (%) | 0.07 | 0.05 | 0.09 |
| Mean age at first event (years) | 55.16 | 55.94 | 54.62 |
| Case fatality at 5-years (%) | 4.11 | 1.67 | 5.81 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 4.0 | 3.0 | 4.0 |
| Recurrence at 6 months (%) | 65.75 | 58.33 | 70.93 |
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