orotic aciduria Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pyrimidine metabolic disorder that is characterized by an excessive secretion of orotic acid in urine. (Human Disease Ontology, DOID_0050833)
External Link http://www.omim.org/entry/258900
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Genes

1 genes associated with the orotic aciduria phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
UMPS uridine monophosphate synthetase