This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
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This is a non-core endpoint: only basic statistics are computed.
See these related core endpoints for full statistics:
E4_LACTOSEINT
lactose intolerance: Inability to fully digest and absorb lactose due to limited or no lactase activity in the small intestine. Congenital intolerance is inherited following an autosomal recessive pattern but is rare. It is more often due to a gradual decline of lactase production in adulthood following the ingestion of fewer lactose-containing foods or secondary to an intestinal mucosal brush-border injury. Prevalence is highest among Asians, Native Americans and Africans. Clinical signs include abdominal cramping, bloating, flatulence and diarrhea following the dietary intake of lactose.
Endpoint definition steps |
FinnGen |
---|---|
Phenotype data |
473681 |
1. Apply sex-specific ruleNone |
473681 |
2. Check conditionsNone |
473681 |
3. Check pre-conditions, main-only, mode, registry filtersRegistry filters: 2 out of 7 registries used, show all original rules. |
835 |
4. Check minimum number of eventsNone |
835 |
5. Include endpoints |
1105 |
6. Filter based on genotype QC (FinnGen only) |
1033 |
Control definitions (FinnGen only)
Extra metadata
List of similar endpoints to Lactose intolerance based on the number of shared cases.
Similar with more cases:
Similar with less cases:
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
All | Female | Male | |
---|---|---|---|
Number of individuals | 1033 | 706 | 327 |
Unadjusted period prevalence (%) | 0.24 | 0.28 | 0.16 |
Median age at first event (years) | 41.25 | 40.23 | 43.45 |
Not a core endpoint, no data to show.
This endpoint is excluded from FinRegistry analyses (omitted endpoint).
Index endpoint: E4_LACTOSEINT – Lactose intolerance
GWS hits: -
This endpoint is excluded from FinRegistry analyses (omitted endpoint).