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

Associations