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bn:01467269n
Noun Concept
SYL
No term available
EN
Haemochromatosis type 3 is a type of Iron overload disorder associated with deficiencies in transferrin receptor 2. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
hemochromatosis
EN
genetic disease
EN
HFE hereditary haemochromatosis
GENETIC ASSOCIATION
EN
transferrin receptor 2

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