No definition available.
Hereditary deficiency of other clotting factors
DOID EFO Endpoint Browser PheWeb
D3_HEREDOTHCLOFACTORS
Endpoint definition
↥
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
520210 |
1. Apply sex-specific ruleNone |
520210 |
2. Check conditionsNone |
520210 |
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters:
2 out of 7 registries used, show all original rules. |
325 |
4. Check minimum number of eventsNone |
325 |
5. Include endpointsNone |
325 |
6. Filter based on genotype QC (FinnGen only) |
325 |
Control definitions (FinnGen only)
- 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 aliorum factorum coagulationis
Similar endpoints
↥List of similar endpoints to Hereditary deficiency of other clotting factors based on the number of shared cases.
Similar with more cases:
- 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 event in hilmo or specialist outpatient
- Any prescribed medicine buy
Similar with less cases:
None
Case counts by codes
↥Summary Statistics
↥-FinRegistry-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | |||
Whole population | 2150 | 1552 | 590 |
Only index persons | 2039 | 1500 | 539 |
Unadjusted period prevalence (%) | |||
Whole population | 0.04 | 0.04 | 0.02 |
Only index persons | 0.05 | 0.06 | 0.02 |
Median age at first event (years) | |||
Whole population | 36.75 | 32.72 | 47.34 |
Only index persons | 36.81 | 32.79 | 47.98 |
-FinnGen-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 325 | 235 | 90 |
Unadjusted period prevalence (%) | 0.07 | 0.08 | 0.04 |
Median age at first event (years) | 42.72 | 37.12 | 57.34 |
-FinRegistry-
Age distribution of first events
-FinnGen-
Age distribution of first events
-FinRegistry-
Year distribution of first events
-FinnGen-
Year distribution of first events
-FinRegistry-
Cumulative Incidence Function
-FinnGen-
Cumulative Incidence Function
CodeWAS (R11)
↥CodeWAS is a tool for exploring the associations between an endpoint and all of the medical codes and drug codes.
This is a new tool, please reach out using the contact form for feedback and improvement ideas.
First, a cohort is built by matching controls to the endpoint cases using year of birth and sex. Then, a Fisher test is done for all the medical codes and drug codes between the cases and controls of this cohort. Codes are reported in the table below if they have −log10(p-value) ≥ 6.
Matched cohort
- Matched cases
- 292
- Matched controls
- 2918
LabWAS
↥Mortality – FinRegistry
↥Association
Association between endpoint D3_HEREDOTHCLOFACTORS and mortality.
Females
Parameter | HR [95% CI] | p-value |
---|---|---|
D3_HEREDOTHCLOFACTORS | 1.209 [0.9, 1.63] | 0.215 |
Birth year | 0.999 [0.99, 1.01] | 0.889 |
During the follow-up period (1.1.1998 — 31.12.2019), 51 out of 1392 females with D3_HEREDOTHCLOFACTORS died.
Males
Parameter | HR [95% CI] | p-value |
---|---|---|
D3_HEREDOTHCLOFACTORS | 1.731 [1.28, 2.33] | < 0.001 |
Birth year | 0.986 [0.98, 1.0] | 0.004 |
During the follow-up period (1.1.1998 — 31.12.2019), 64 out of 470 males with D3_HEREDOTHCLOFACTORS died.
Mortality risk
Mortality risk for people of age
years, who have D3_HEREDOTHCLOFACTORS.N-year risk | Females | Males |
---|---|---|
1 | 0.131% | 0.313% |
5 | 0.801% | 2.019% |
10 | 2.02% | 4.984% |
15 | 3.777% | 8.99% |
20 | 6.841% | 15.016% |
Relationships between endpoints
↥Index endpoint: D3_HEREDOTHCLOFACTORS – Hereditary deficiency of other clotting factors
GWS hits: 13