Muscle wasting and atrophy, not elsewhere classified

M13_MUSCLEATROPH

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

Endpoint definition

FinnGen phenotype data

392423 individuals

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Apply sex-specific rule None

392423

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Check conditions None

392423

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Check pre-conditions, main-only, mode, registry filters

Hospital Discharge: ICD-10 M62.5
Hospital discharge: ICD-9 7282A
Hospital discharge: ICD-8 7331
Cause of death: ICD-10 M62.5
Cause of death: ICD-9 7282A
Cause of death: ICD-8 7331

2 out of 7 registries used, show all original rules.

166

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Check minimum number of events None

166

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Include endpoints None

166

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Remove individuals based on genotype QC

163

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M13_MUSCLEATROPH

Control definitions

Control exclude M13_SOFTTISSUE

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M62
Name in latin Atrophia et degeneratio musculi non alibi classificatae

Summary Statistics

Key figures

All Female Male
Number of individuals 163 82 81
Unadjusted prevalence (%) 0.04 0.04 0.05
Mean age at first event (years) 55.71 52.50 58.96

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: M13_MUSCLEATROPH – Muscle wasting and atrophy, not elsewhere classified
GWS hits:

Survival analyses between endpoints

Plot

before Muscle wasting and atrophy, not elsewhere classified
after Muscle wasting and atrophy, not elsewhere classified

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Muscle wasting and atrophy, not elsewhere classified

Endpoint not on priority list, no data to show.