pyrimidine-responsive megaloblastic anemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of megaloblastic anemia that improves upon administration of pyrimidine supplements such as uridylic acid and cytidylic acid. (Human Phenotype Ontology, HP_0003339)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003339
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Genes

1 genes associated with the pyrimidine-responsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
UMPS uridine monophosphate synthetase