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bn:01467269n
Noun Concept
Categories: Iron metabolism, Red blood cell disorders
EN
Haemochromatosis type 3  hemochromatosis type 3  HEMOCHROMATOSIS, TYPE 3  HEMOCHROMATOSIS, TYPE 3; HFE3  Hemochromatosis Due to Defect 1N Transferrin Receptor 2
EN
Haemochromatosis type 3 is a type of Iron overload disorder associated with deficiencies in transferrin receptor 2. Wikipedia
Definitions
Relations
Sources
EN
Haemochromatosis type 3 is a type of Iron overload disorder associated with deficiencies in transferrin receptor 2. Wikipedia
Hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22 Wikidata
IS A
rare disease
hemochromatosis
genetic disease
HFE hereditary haemochromatosis
GENETIC ASSOCIATION
transferrin receptor 2
Wikipedia
EN
Haemochromatosis type 3
Wikidata
EN
hemochromatosis type 3
Wikidata Alias
EN
HEMOCHROMATOSIS, TYPE 3, HEMOCHROMATOSIS, TYPE 3; HFE3, Hemochromatosis Due to Defect 1N Transferrin Receptor 2, hemochromatosis due to defect in transferrin receptor 2, HFE3, TFR2-related hemochromatosis

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