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
D68.1
Hospital discharge: ICD-9
2862
Hospital discharge: ICD-8
28620
Cause of death: ICD-10
D68.1
Cause of death: ICD-9
2862
Cause of death: ICD-8
28620
2 out of 7 registries used, show all original rules.
12
Check minimum number of events None
12
Include endpoints None
12
Remove individuals based on genotype QC
11
D3_HEREDFXIDEF
Control definitions
Control exclude
D3_COAGDEF_PURPUR_HAEMORRHAGIC
Extra metadata
Level in the ICD hierarchy
4
First used in FinnGen datafreeze
DF2
Parent code in ICD-10
D68
Name in latin
Deficientia hereditaria factoris XI
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to
Hereditary factor XI deficiency
based on the number of shared cases.
Broader endpoints:
- Other coagulation defects
- Coagulation defects, purpura and other haemorrhagic conditions
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
- Any operation in hilmo
- Any event in hilmo or specialist outpatient
Narrower endpoints:
None
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 11 | 8 | - |
| Unadjusted prevalence (%) | 0.00 | 0.00 | - |
| Mean age at first event (years) | 47.22 | 38.27 | - |
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: D3_HEREDFXIDEF – Hereditary factor XI deficiency
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Hereditary factor XI deficiency
↥Endpoint not on priority list, no data to show.