Systemic connective tissue disorders
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 | M13_SYSTCONNECT |
| Include | M13_POLYARTERETAL, M13_NECROVASC, M13_SLE, M13_DERMATOPOLY, M13_SYSTSLCE, M13_OTHCONN |
| Level in the ICD-hierarchy | 2 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 4177 | 3180 | 997 |
| Unadjusted prevalence (%) | 2.4 | 3.21 | 1.33 |
| Mean age at first event (years) | 54.42 | 53.32 | 57.95 |
| Case fatality at 5-years (%) | 4.81 | 3.65 | 8.53 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 3 | 3 | 2 |
| Recurrence at 6 months (%) | 56.94 | 57.57 | 54.96 |
Associations
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