|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine. (Human Disease Ontology, DOID_0050727)|
|Downloads & Tools|
1 genes associated with the tyrosinemia, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.