tyrosinemia type III

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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.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hpd

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010162 - tyrosinemia type III

MONDO:0010162 - tyrosinemia type III

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): tyrosinemia (is_a)