DISEASES

Disease-gene associations mined from literature

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