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.
| Name | G6_OTHINMUSC |
|---|---|
| Long name | Other inherited muscular atrophy |
| 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 |
| Latin name | Alia atrophia musculorum spinalis congenita |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 20 | 8 | 12 |
| Unadjusted prevalence (%) | 0.01 | 0.01 | 0.01 |
| Mean age at first event (years) | 52.06 | 52.48 | 51.78 |
| Case fatality at 5-years (%) | 10.00 | 0.00 | 16.67 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 2.5 | 1.5 | 5.0 |
| Recurrence at 6 months (%) | 50.00 | 37.50 | 58.33 |
before Other inherited muscular atrophy
after Other inherited muscular atrophy
Loading survival analyses plot…
Loading survival analyses table…