Other inherited muscular atrophy
Description
amyotrophic lateral sclerosis: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord.
Data source
| FinnGen phenocode | G6_OTHINMUSC |
| Hospital Discharge registry | ICD-10: G121, ICD-9: 3351A |
| Cause of Death registry | ICD-10: G121, ICD-9: 3351A |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 15 | - | 11 |
| Unadjusted prevalence (%) | 0.01 | - | 0.01 |
| Mean age at first event (years) | 59.64 | - | 56.37 |
| Case fatality at 5-years (%) | 13.33 | - | 18.18 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 3 | - | 3 |
| Recurrence at 6 months (%) | 53.33 | - | 54.55 |
Associations
Loading associations…