Other and unspecified spinal muscular atrophies

G6_SPINAMUSCOTH

spinal muscular atrophy: Spinal muscular atrophy is a disorder of spinal motor neurons characterized clinically by the development of muscle weakness and atrophy.

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 G12.8, G12.9, G13*
Hospital discharge: ICD-9 335
Hospital discharge: ICD-8 34829|3489
Hospital discharge: excluded ICD-9 3350A|3351A|3352A
Cause of death: ICD-10 G12.8, G12.9, G13*
Cause of death: ICD-9 335
Cause of death: ICD-8 34829|3489

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

222

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Check minimum number of events None

222

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Include endpoints None

222

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Remove individuals based on genotype QC

219

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G6_SPINAMUSCOTH

Control definitions

Control exclude G6_NEUATR

Extra metadata

Level in the ICD hierarchy 3
First used in FinnGen datafreeze DF2

Summary Statistics

Key figures

All Female Male
Number of individuals 219 80 139
Unadjusted prevalence (%) 0.06 0.04 0.08
Mean age at first event (years) 56.45 48.87 60.81

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: G6_SPINAMUSCOTH – Other and unspecified spinal muscular atrophies
GWS hits: 8

Survival analyses between endpoints

Plot

before Other and unspecified spinal muscular atrophies
after Other and unspecified spinal muscular atrophies

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Other and unspecified spinal muscular atrophies

Endpoint not on priority list, no data to show.