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bn:04870443n
Noun Concept
NL
No term available
EN
rare severe gastrointestinal disorder in newborns primarily reported in Finland Wikidata
Relations
Sources
IS A
ziekte
EN
Inborn errors of carbohydrate metabolism
EN
autosomal recessive disease
EN
lactase deficiency
PART OF
finse erfgoed ziekte
GENETIC ASSOCIATION
LCT
HAS EFFECT
lactose-intolerantie

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