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

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