Hereditary monor and sensory neuropathy

G6_HEREMOSEN

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).']

Endpoint definition

FinnGen phenotype data

356077 individuals

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Apply sex-specific rule None

356077

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Check conditions None

356077

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Filter registries

Hospital Discharge: ICD-10 G60.0
Hospital discharge: ICD-9 3560
Hospital discharge: ICD-8 33000
Cause of death: ICD-10 G60.0
Cause of death: ICD-9 3560
Cause of death: ICD-8 33000

254

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Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9

203

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Check minimum number of events None

203

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Include endpoints None

203

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G6_HEREMOSEN

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 G60
Name in latin Neuropathia motoria et sensoria hereditaria

Summary Statistics

Key figures

All Female Male
Number of individuals 203 106 97
Unadjusted prevalence (%) 0.06 0.05 0.06
Mean age at first event (years) 45.80 43.79 47.99

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

Index endpoint: G6_HEREMOSEN – Hereditary monor and sensory neuropathy
GWS hits: 2

Survival analyses between endpoints

Plot

before Hereditary monor and sensory neuropathy
after Hereditary monor and sensory neuropathy

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Hereditary monor and sensory neuropathy