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bn:03540354n
Noun Concept
SYL
No term available
EN
Hereditary haemochromatosis type 1 is a genetic disorder characterized by excessive intestinal absorption of dietary iron, resulting in a pathological increase in total body iron stores. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
hemochromatosis
EN
metal metabolism disorder
HAS KIND
EN
juvenile hemochromatosis
EN
Haemochromatosis type 3
EN
African iron overload
EN
hemochromatosis type 5
DRUG USED FOR TREATMENT
EN
deferoxamine
EN
deferasirox
EN
deferiprone
GENETIC ASSOCIATION
EN
HFE
HAS EFFECT
EN
cirrhosis
HEALTH SPECIALTY
EN
endocrinology
EN
hepatology

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