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 | 11 | N/A | 6 |
| Unadjusted prevalence (%) | 0.01 | N/A | 0.01 |
| Mean age at first event (years) | 48.59 | N/A | 54.98 |
| Median number of events / individual | 1 | N/A | 1 |
Clinical metrics
| Sex | All | Female | Male |
| Recurrence within 6 months (%) | 36.36 | N/A | 33.33 |
| Case fatality at 5-years (%) | 0.0 | N/A | 0.0 |