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bn:03540354n
Noun Concept
JA
ヘモクロマトーシス  遺伝性血色素症
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
希少疾患
鉄過剰症
EN
metal metabolism disorder
HAS KIND
EN
juvenile hemochromatosis
EN
Haemochromatosis type 3
バンツー血鉄症
EN
hemochromatosis type 5
DRUG USED FOR TREATMENT
デフェロキサミン
デフェラシロクス
デフェリプロン
GENETIC ASSOCIATION
EN
HFE
HAS EFFECT
肝硬変
HEALTH SPECIALTY
内分泌学
肝臓学
Wikidata
JA
ヘモクロマトーシス
Wikidata Alias
JA
遺伝性血色素症

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