Human genes for tyrosinemia type III
Tyrosinemia type III [DOID:0050727]
A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine.
Synonyms: tyrosinemia type III, DOID:0050727, tyrosinemia type IIIs
Linkouts: OMIM