Other systemic involvement of connective tissue (FG)
Description
connective tissue disease: A disorder characterized by abnormalities in one or more of the elements of the connective tissues, typically associated with genetic defects.
Data source
| FinnGen phenocode | OTHER_SYSTCON_FG |
| Include | M13_SJOGREN, M13_OVERLAP, M13_BEHCET, M13_POLYMYALGIA, M13_HYPERMOBILITY, M13_CONNECTNAS |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 3076 | 2424 | 652 |
| Unadjusted prevalence (%) | 1.76 | 2.44 | 0.87 |
| Mean age at first event (years) | 55.31 | 53.93 | 60.42 |
| Case fatality at 5-years (%) | 4.1 | 3.09 | 7.82 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 2 | 2 | 2 |
| Recurrence at 6 months (%) | 52.03 | 52.95 | 48.62 |
Associations
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