abnormality of tyrosine metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a tyrosine metabolic process. (Human Phenotype Ontology, HP_0010917)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010917
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Genes

3 genes associated with the abnormality of tyrosine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
HPD 4-hydroxyphenylpyruvate dioxygenase
TAT tyrosine aminotransferase