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Motor neuron disease (with DMD)

DOIDEFOMESH PheWeb

muscular disease: Acquired, familial, and congenital disorders of skeletal muscle and smooth muscle.

Endpoint definition

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FinnGen phenotype data
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Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 G71.06
Cause of death: ICD-10 G71.06

Check pre-conditions None

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Include endpoints

Check conditions None

Apply sex-specific rule None

diagram downward connector MND

Extra metadata

First used in FinnGen datafreeze DF3
Parent code in ICD-10 G710
Name in latin Dystrophia musculorum gravis (Duchenne)

Summary Statistics

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Key figures

All Female Male
Number of individuals 277 104 173
Unadjusted prevalence (%) 0.11 0.07 0.15
Mean age at first event (years) 60.89 62.66 59.83

Mortality

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

Correlations

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Index endpoint: MND – Motor neuron disease (with DMD)
GWS hits: 3

Survival analyses between endpoints

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Plot

before Motor neuron disease (with DMD)
after Motor neuron disease (with DMD)

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Motor neuron disease (with DMD)

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