|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormal decrease in orotidine 5'-phosphate decarboxylase activity. (Human Phenotype Ontology, HP_0003267)|
|Downloads & Tools|
1 genes associated with the reduced orotidine 5-prime phosphate decarboxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|UMPS||uridine monophosphate synthetase|