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Tyrosinemia type III
rareTyrosinemia type 3 is an inborn error of tyrosine metabolism characterized by mild hypertyrosinemia and increased urinary excretion of 4-hydroxyphenylpyruvate, 4-hydroxyphenyllactate and 4-hydroxyphenylacetate.
- Identifiers
- MONDO:0010162 OMIM:276710Orphanet:69723
- Causal genes
- HPD
- Part of
- Tyrosinemia
- Also known as
- 4-alpha hydroxyphenylpyruvate dioxygenase deficiency · 4-alpha hydroxyphenylpyruvic acid oxidase deficiency · tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency · tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency · tyrosinemia due to HPD deficiency
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