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Muscle wasting and atrophy, not elsewhere classified

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 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

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_MUSCLEATROPH

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

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Key figures

All Female Male
Number of individuals 97 47 50
Unadjusted prevalence (%) 0.04 0.03 0.04
Mean age at first event (years) 52.06 49.09 54.87

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_MUSCLEATROPH – Muscle wasting and atrophy, not elsewhere classified
GWS hits: 0

Survival analyses between endpoints

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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

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