Other systemic involvement of connective tissue
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_OTHCONN |
| Hospital Discharge registry | ICD-10: M35 |
| Cause of Death registry | ICD-10: M35 |
| Include | M13_SJOGREN, M13_OVERLAP, M13_BEHCET, M13_POLYMYALGIA, M13_DIFFASCITIS, M13_MULTIFIBRO, M13_WEBERCHRISTIAN, M13_HYPERMOBILITY, M13_CONNECTNAS, M13_SYSTCONINOTH |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 3142 | 2464 | 678 |
| Unadjusted prevalence (%) | 1.8 | 2.48 | 0.9 |
| Mean age at first event (years) | 55.16 | 53.83 | 60.01 |
| Case fatality at 5-years (%) | 4.26 | 3.21 | 8.11 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 2 | 2 | 2 |
| Recurrence at 6 months (%) | 51.89 | 52.86 | 48.38 |
Associations
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