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Summary Literature (0)
DOID:0050727 - tyrosinemia type III

Disease Ontology Definition:A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine.


OMIM:276710 - tyrosinemia, type iii; tyrsn3

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Echinobase Genes : hpd

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): tyrosinemia (is_a)