No definition available.
Endpoint definition
↥Report an error or suggest an improvement for this endpoint codes
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. |
166 |
4. Check minimum number of eventsNone |
166 |
5. Include endpointsNone |
166 |
6. Filter based on genotype QC (FinnGen only) |
166 |
Control definitions (FinnGen only)
- Control exclude
- Q17_OTHER_CONGEN_MALFO_DIGES_SYSTEM1
Extra metadata
- Level in the ICD hierarchy
- 3
- First used in FinnGen datafreeze
- DF4
- Parent code in ICD-10
- Q3[8-9]|Q4[0-5]
- Name in latin
- Malformationes congenitae oesophagi
Similar endpoints
↥List of similar endpoints to
Congenital malformations of oesophagus
based on the number of shared cases.
Similar with more cases:
- Other congenital malformations of the digestive system
- Congenital malformations, deformations and chromosomal abnormalities
- Any operation in hilmo
- Any event in hilmo or specialist outpatient
Similar with less cases:
None
Case counts by codes
↥Summary Statistics
↥-FinRegistry-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | |||
Whole population | 1406 | 640 | 758 |
Only index persons | 1057 | 489 | 568 |
Unadjusted period prevalence (%) | |||
Whole population | 0.02 | 0.02 | 0.02 |
Only index persons | 0.02 | 0.02 | 0.02 |
Median age at first event (years) | |||
Whole population | 21.73 | 34.07 | 10.71 |
Only index persons | 35.77 | 49.40 | 24.03 |
-FinnGen-
Key figures
All | Female | Male | |
---|---|---|---|
Number of individuals | 166 | 73 | 93 |
Unadjusted period prevalence (%) | 0.03 | 0.02 | 0.04 |
Median age at first event (years) | 58.90 | 56.70 | 60.63 |
-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
- 141
- Matched controls
- 1411
LabWAS
↥Mortality – FinRegistry
↥Association
Association between endpoint Q17_CONGEN_MALFO_OESOPHAGUS and mortality.
Females
Parameter | HR [95% CI] | p-value |
---|---|---|
Q17_CONGEN_MALFO_OESOPHAGUS | 1.319 [0.99, 1.76] | 0.062 |
Birth year | 0.992 [0.98, 1.0] | 0.098 |
During the follow-up period (1.1.1998 — 31.12.2019), 92 out of 492 females with Q17_CONGEN_MALFO_OESOPHAGUS died.
Males
Parameter | HR [95% CI] | p-value |
---|---|---|
Q17_CONGEN_MALFO_OESOPHAGUS | 1.592 [1.12, 2.26] | 0.009 |
Birth year | 0.988 [0.98, 1.0] | 0.033 |
During the follow-up period (1.1.1998 — 31.12.2019), 92 out of 579 males with Q17_CONGEN_MALFO_OESOPHAGUS died.
Mortality risk
Mortality risk for people of age
years, who have Q17_CONGEN_MALFO_OESOPHAGUS.N-year risk | Females | Males |
---|---|---|
1 | 0.147% | 0.364% |
5 | 0.706% | 2.122% |
10 | 1.784% | 5.113% |
15 | 3.469% | 8.932% |
20 | 6.047% | 14.384% |
Relationships between endpoints
↥Index endpoint: Q17_CONGEN_MALFO_OESOPHAGUS – Congenital malformations of oesophagus
GWS hits: -