tyrosinemia type iii Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine. (Human Disease Ontology, DOID_0050727)
Similar Terms
Downloads & Tools

Genes

4 genes co-occuring with the disease tyrosinemia type iii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HPD 4-hydroxyphenylpyruvate dioxygenase 2.03921
EN1 engrailed homeobox 1 1.32978
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase) 1.17292
TAT tyrosine aminotransferase 0.880653