≡ Risteys
R8

Documentation Changelog GitHub Contact & Feedback

Muscle wasting and atrophy, not elsewhere classified

DOID EFO MESH PheWeb

M13_MUSCLEATROPH

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

Endpoint definition

↥
FinnGen phenotype data

356077 individuals

diagram downward connector

Apply sex-specific rule None

356077

diagram downward connector

Check conditions None

356077

diagram downward connector
diagram bullet

Filter registries

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

174

diagram downward connector
diagram bullet

Check pre-conditions, main-only, mode, ICD version

Look only at ICD versions H.D: 10, 8, 9 ; C.O.D: 10, 8, 9

145

diagram downward connector

Check minimum number of events None

145

diagram downward connector

Include endpoints None

145

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

↥

Key figures

All Female Male
Number of individuals 145 70 75
Unadjusted prevalence (%) 0.04 0.04 0.05
Mean age at first event (years) 55.76 52.74 58.58

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

↥