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
D67
Hospital discharge: ICD-9
2861
Hospital discharge: ICD-8
2861
Cause of death: ICD-10
D67
Cause of death: ICD-9
2861
Cause of death: ICD-8
2861
2 out of 7 registries used, show all original rules.
19
Check minimum number of events None
19
Include endpoints None
19
Remove individuals based on genotype QC
18
D3_HEREDFIXDEF
Control definitions
Control exclude
D3_COAGDEF_PURPUR_HAEMORRHAGIC
Extra metadata
Level in the ICD hierarchy
3
First used in FinnGen datafreeze
DF2
Parent code in ICD-10
D65-D69
Name in latin
Deficientia hereditaria factoris IX
Show upset plot detailing case counts by codes
Or the full data table
Similar endpoints
↥List of similar endpoints to
Hereditary factor IX deficiency
based on the number of shared cases.
Broader endpoints:
- 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
- Any prescribed medicine buy
Narrower endpoints:
None
Summary Statistics
↥Key figures
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 18 | 7 | 11 |
| Unadjusted prevalence (%) | 0.00 | 0.00 | 0.01 |
| Mean age at first event (years) | 27.70 | 35.47 | 22.75 |
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_HEREDFIXDEF – Hereditary factor IX deficiency
GWS hits:
Survival analyses between endpoints
↥Not a core endpoint, no data to show.
Drugs most likely to be purchased after Hereditary factor IX deficiency
↥Endpoint not on priority list, no data to show.