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Summary Literature (0)
DOID:9275 - tyrosinemia

Disease Ontology Definition:An amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine.

Synonyms:

Xenbase Genes : hpd, fah, tat

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0004741 - tyrosinemia


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amino acid metabolic disorder (is_a)