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