Muscle wasting and atrophy, not elsewhere classified
Description
muscular disease: Acquired, familial, and congenital disorders of skeletal muscle and smooth muscle.
Data source
| FinnGen phenocode | M13_MUSCLEATROPH |
| Hospital Discharge registry | ICD-10: M625, ICD-9: 7282A, ICD-8: 7331 |
| Cause of Death registry | ICD-10: M625, ICD-9: 7282A, ICD-8: 7331 |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 62 | 27 | 35 |
| Unadjusted prevalence (%) | 0.04 | 0.03 | 0.05 |
| Mean age at first event (years) | 55.65 | 57.29 | 54.38 |
| Case fatality at 5-years (%) | 6.45 | 3.7 | 8.57 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 1 | 1 | 1 |
| Recurrence at 6 months (%) | 32.26 | 29.63 | 34.29 |
Associations
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