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).']
| Name | G6_HEREMOSEN |
|---|---|
| Long name | Hereditary monor and sensory neuropathy |
| 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 |
| Latin name | Neuropathia motoria et sensoria hereditaria |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 98 | 53 | 45 |
| Unadjusted prevalence (%) | 0.05 | 0.04 | 0.05 |
| Mean age at first event (years) | 45.54 | 41.84 | 49.89 |
| Case fatality at 5-years (%) | 3.06 | 1.89 | 4.44 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 3.0 | 4.0 | 2.0 |
| Recurrence at 6 months (%) | 54.08 | 60.38 | 46.67 |
before Hereditary monor and sensory neuropathy
after Hereditary monor and sensory neuropathy
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