Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0050832 - pyrimidine metabolic disorder

Disease Ontology Definition:An inherited metabolic disorder involving dysfunction of pyrimidine metabolism.

Synonyms:

Xenbase Genes : dpys, umps

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019238 - inborn disorder of pyrimidine metabolism


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): inherited metabolic disorder (is_a)