Common variable immunodeficiency with predominant abnormalities of T-cell numbers and function
Description
No definition available.
Data source
| FinnGen phenocode | D3_CVID_TCELL |
| Hospital Discharge registry | ICD-10: D831, ICD-9: 2791X |
| Cause of Death registry | ICD-10: D831, ICD-9: 2791X |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 13 | 10 | N/A |
| Unadjusted prevalence (%) | 0.01 | 0.01 | N/A |
| Mean age at first event (years) | 58.34 | 58.33 | N/A |
| Median number of events / individual | 1 | 1 | N/A |
Clinical metrics
| Sex | All | Female | Male |
| Recurrence within 6 months (%) | 30.77 | 30.0 | N/A |
| Case fatality at 5-years (%) | 15.38 | 20.0 | N/A |