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Muscular dystrophy

DOID EFO MESH PheWeb

G6_MUSDYST

obsolete_muscular dystrophy: ['An atrophic muscular disease that causes progressive weakness and degeneration of skeletal muscles used during voluntary movement.']

Endpoint definition

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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 G71.0
Hospital discharge: ICD-9 3591A
Hospital discharge: ICD-8 33030|33090
Cause of death: ICD-10 G71.0
Cause of death: ICD-9 3591A
Cause of death: ICD-8 33030|33090

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

219

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Check minimum number of events None

219

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Include endpoints None

219

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Remove individuals based on genotype QC

210

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G6_MUSDYST

Control definitions

Control exclude G6_MYONEU

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2
Parent code in ICD-10 G71
Name in latin Dystrophia musculorum (progressiva hereditaria)

Summary Statistics

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Key figures

All Female Male
Number of individuals 210 110 100
Unadjusted prevalence (%) 0.06 0.05 0.06
Mean age at first event (years) 45.04 49.31 40.33

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: G6_MUSDYST – Muscular dystrophy
GWS hits: 19

Survival analyses between endpoints

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Plot

before Muscular dystrophy
after Muscular dystrophy

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Muscular dystrophy

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Endpoint not on priority list, no data to show.