ICD-9 / Health Information

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

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MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D020176 |4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency (also called Hawkinsinuria) is an autosomal dominant inborn error of metabolism. It is characterised by transient metabolic acidosis and tyrosinemia.

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