Tyrosinemia type III

Tyrosinemia 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.

Also known as: tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency, tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency, tyrosinemia due to HPD deficiency, tyrosinemia type III, 4-Hydroxyphenylpyruvate dioxygenase deficiency, 4-Hydroxyphenylpyruvic acid oxidase deficiency, 4-alpha hydroxyphenylpyruvate dioxygenase deficiency, 4-alpha hydroxyphenylpyruvic acid oxidase deficiency

0 clinical trials for this condition and its sub-types.