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Dsorders of muscle in diseases classified elsewhere

DOID EFO MESH PheWeb

M13_MUSCLEINOTH

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

Endpoint definition

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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 M63
Hospital discharge: ICD-9 $!$
Hospital discharge: ICD-8 $!$
Cause of death: ICD-10 M63
Cause of death: ICD-9 $!$
Cause of death: ICD-8 $!$

31

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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

31

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Check minimum number of events None

31

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Include endpoints None

31

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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 31 22 9
Unadjusted prevalence (%) 0.01 0.01 0.01
Mean age at first event (years) 47.76 39.58 67.75

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

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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

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

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