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Hereditary hyperbilirubinemia
・ Hereditary inclusion body myopathy
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Hereditary hyperbilirubinemia : ウィキペディア英語版
Hereditary hyperbilirubinemia

Hereditary hyperbilirubinemia refers to the condition where levels of bilirubin are elevated, for reasons that can be attributed to a metabolic disorder.
An example is Crigler-Najjar syndrome.
==Symptoms==
UGT1A1 gene mutations causes the condition. As a result, there can be reduced functionality of the bilirubin-UGT enzyme. Eventually it causes unconjugated hyperbilirubinemia and jaundice as substance accumulates in the body due to the reduced ability of the enzyme.〔http://ghr.nlm.nih.gov/condition/crigler-najjar-syndrome〕

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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