Tyrosinemia type 3

From BugSigDB


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.
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