Hereditary monor and sensory neuropathy
Description
charcot-marie-tooth disease, axonal, type 2t: ['Charcot-Marie-Tooth disease type 2T (CMT2T) is a slowly progressive autosomal recessive sensorimotor peripheral neuropathy with onset in middle age (Higuchi et al., 2016).']
Data source
| FinnGen phenocode | G6_HEREMOSEN |
| Hospital Discharge registry | ICD-10: G600, ICD-8: 33000 |
| Cause of Death registry | ICD-10: G600, ICD-8: 33000 |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 80 | 42 | 38 |
| Unadjusted prevalence (%) | 0.05 | 0.04 | 0.05 |
| Mean age at first event (years) | 46.04 | 42.38 | 50.07 |
| Case fatality at 5-years (%) | 1.25 | 0.0 | 2.63 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 3 | 4 | 2 |
| Recurrence at 6 months (%) | 55.0 | 61.9 | 47.37 |
Associations
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