tyrosinemia, type iii Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine. (Human Disease Ontology, DOID_0050727)
External Link http://www.omim.org/entry/276710
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Genes

1 genes associated with the tyrosinemia, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HPD 4-hydroxyphenylpyruvate dioxygenase