Hereditary factor VIII deficiency
Description
obsolete_factor VIII deficiency: An X-linked disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
Data source
| FinnGen phenocode | D3_HEREDFVIIIDEF |
| Hospital Discharge registry | ICD-10: D66, ICD-8: 2860 |
| Cause of Death registry | ICD-10: D66, ICD-8: 2860 |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 26 | 11 | 15 |
| Unadjusted prevalence (%) | 0.01 | 0.01 | 0.02 |
| Mean age at first event (years) | 34.3 | 38.42 | 31.28 |
| Case fatality at 5-years (%) | 7.69 | 0.0 | 13.33 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 2 | 2 | 4 |
| Recurrence at 6 months (%) | 42.31 | 27.27 | 53.33 |
Associations
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