Myasthenia gravis

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_MYASTHENIA
Hospital Discharge registry ICD-8: 7330
Cause of Death registry ICD-8: 7330
KELA reimboursements codes 108
Level in the ICD-hierarchy 3
First defined in version DF2
Ontology
DOID 437
GWAS catalog 0004991
MESH D009157
SNOMED CT 91637004

Key figures

Sex All Female Male
Number of individuals 178 99 79
Unadjusted prevalence (%) 0.1 0.1 0.11
Mean age at first event (years) 51.54 45.93 58.56
Case fatality at 5-years (%) 4.49 5.05 3.8

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 7 10 4
Recurrence at 6 months (%) 68.54 72.73 63.29

Associations

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