This is a non-core endpoint: only basic statistics are computed.
Endpoint definition
↥
FinnGen phenotype data
429209 individuals
Apply sex-specific rule None
429209
Check conditions None
429209
Check pre-conditions, main-only, mode, registry filters
Hospital Discharge: ICD-10
G12.0
Hospital discharge: ICD-9
3350A
Hospital discharge: ICD-8
33010
Cause of death: ICD-10
G12.0
Cause of death: ICD-9
3350A
Cause of death: ICD-8
33010
2 out of 7 registries used, show all original rules.
20
Check minimum number of events None
20
Include endpoints None
20
Remove individuals based on genotype QC
20
G6_INFAMUSC
Control definitions
Control exclude
G6_NEUATR
Extra metadata
Level in the ICD hierarchy
3
First used in FinnGen datafreeze
DF2
Parent code in ICD-10
G12
Name in latin
Atrophia musculorum spinalis infantilis, typus I (Werdnig-Hoffmann)
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to
Infantile muscular atrophy
based on the number of shared cases.
Broader endpoints:
- Systemic atrophies primarily affecting the central nervous system
- Neurological diseases
- Neurological diseases
- Any operation in hilmo
- Any event in hilmo or specialist outpatient
Narrower endpoints:
None
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 20 | 10 | 10 |
| Unadjusted prevalence (%) | 0.00 | 0.00 | 0.01 |
| Mean age at first event (years) | 40.85 | 25.21 | 56.48 |
Mortality
Not a core endpoint, no data to show.
Age distribution of first events
Year distribution of first events
Cumulative Incidence
Not a core endpoint, no data to show.
Correlations
↥
Index endpoint: G6_INFAMUSC – Infantile muscular atrophy
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Infantile muscular atrophy
↥Endpoint not on priority list, no data to show.