Congenital and developmental myasthenia
Description
Myasthenia gravis: Myasthenia gravis (MG) is a rare, clinically heterogeneous, autoimmune disorder of the neuromuscular junction characterized by fatigable weakness of voluntary muscles.
Data source
| FinnGen phenocode | G6_CONDEVMYA |
| Hospital Discharge registry | ICD-10: G702 |
| Cause of Death registry | ICD-10: G702 |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 9 | - | - |
| Unadjusted prevalence (%) | 0.01 | - | - |
| Mean age at first event (years) | 62.05 | - | - |
| Case fatality at 5-years (%) | 22.22 | - | - |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 1 | - | - |
| Recurrence at 6 months (%) | 11.11 | - | - |
Associations
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