|OBO ID: DOID:0050727|
|Term Name:||tyrosinemia type III||Search Ontology:|
|Definition:||A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine. (2)|
|Ontology:||Human Disease (DOID:0050727)|
|is a type of:||
OTHER tyrosinemia type III PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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