Tyrosinemia type 3

Tyrosinemia type 3 is an inborn error of tyrosine metabolism characterised by mild hypertyrosinemia and increased urinary excretion of 4-hydroxyphenylpyruvate, 4-hydroxyphenyllactate and 4-hydroxyphenylacetate.

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Aliases

• 4-alpha hydroxyphenylpyruvate dioxygenase deficiency
• 4-alpha hydroxyphenylpyruvic acid oxidase deficiency
• 4-Hydroxyphenylpyruvate dioxygenase deficiency
• 4-Hydroxyphenylpyruvic acid oxidase deficiency
• Tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency
• tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency
• Tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency
• tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency
• Tyrosinemia due to HPD deficiency
• tyrosinemia due to HPD deficiency
• tyrosinemia type 3
• Tyrosinemia type III
• tyrosinemia type III
• tyrosinemia type III
• tyrosinemia, type 3
• tyrosinemia, type III
• TYRSN3