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UDP glucuronyl transferase deficiency

Introduction: UDP glucuronyl transferase deficiency

Description of UDP glucuronyl transferase deficiency

UDP glucuronyl transferase deficiency: A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
Source: Diseases Database

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Source: Diseases Database

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Source: Diseases Database

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