Congenital lactase deficiency

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

FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 E73.0
Cause of death: ICD-10 E73.0

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector E4_LACTOCON

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 E73
Name in latin Deficientia lactasae congenita

Summary Statistics

Key figures

All Female Male
Number of individuals 36 27 9
Unadjusted prevalence (%) 0.01 0.02 0.01
Mean age at first event (years) 38.80 37.83 41.71

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Correlations

Index endpoint: E4_LACTOCON – Congenital lactase deficiency
GWS hits:

Survival analyses between endpoints

Plot

before Congenital lactase deficiency
after Congenital lactase deficiency

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Drugs most likely to be purchased after Congenital lactase deficiency