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Dsorders of muscle in diseases classified elsewhere

DOIDEFOMESH PheWeb

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

Endpoint definition

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FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 M63
Cause of death: ICD-10 M63

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_MUSCLEINOTH

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M60-M63
Name in latin Morbositates musculorum in morbis alibi classificatis

Summary Statistics

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Key figures

All Female Male
Number of individuals 24 16 8
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 50.40 41.69 67.81

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: M13_MUSCLEINOTH – Dsorders of muscle in diseases classified elsewhere
GWS hits:

Survival analyses between endpoints

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Plot

before Dsorders of muscle in diseases classified elsewhere
after Dsorders of muscle in diseases classified elsewhere

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Dsorders of muscle in diseases classified elsewhere

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