Metabolic disorder, other/unspecified
Description
metabolic disease: A congenital (due to inherited enzyme abnormality) or acquired (due to failure of a metabolic important organ) disorder resulting from an abnormal metabolic process.
Data source
| FinnGen phenocode | E4_METABONAS |
| Hospital Discharge registry | ICD-10: E889 |
| Cause of Death registry | ICD-10: E889 |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 23 | 12 | 11 |
| Unadjusted prevalence (%) | 0.01 | 0.01 | 0.01 |
| Mean age at first event (years) | 37.89 | 29.32 | 47.24 |
| Case fatality at 5-years (%) | 0.0 | 0.0 | 0.0 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 1 | 1 | 1 |
| Recurrence at 6 months (%) | 34.78 | 41.67 | 27.27 |
Associations
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