Congenital lactase deficiency

E4_LACTOCON

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

429209 individuals

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Apply sex-specific rule None

429209

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Check conditions None

429209

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Check pre-conditions, main-only, mode, registry filters

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

2 out of 7 registries used, show all original rules.

68

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Check minimum number of events None

68

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Include endpoints None

68

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Remove individuals based on genotype QC

61

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E4_LACTOCON

Control definitions

Control exclude E4_METABOLIA

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 61 45 16
Unadjusted prevalence (%) 0.01 0.02 0.01
Mean age at first event (years) 41.73 40.95 43.90

Mortality

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

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

Index endpoint: E4_LACTOCON – Congenital lactase deficiency
GWS hits: 1

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

Endpoint not on priority list, no data to show.