Tyrosinemia type 3
Synonyms: Tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency | Tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency | Tyrosinemia due to HPD deficiency | Tyrosinemia type III
A rare inborn error of tyrosine metabolism characterized by mild hypertyrosinemia and increased urinary excretion of 4-hydroxyphenylpyruvate 4-hydroxyphenyllactate and 4-hydroxyphenylacetate.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024
Newly diagnosed with
Tyrosinemia type 3?
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