purine-pyrimidine metabolic disorder

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Summary

Literature (0)

DOID:653 - purine-pyrimidine metabolic disorder

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

Synonyms: inborn errors of purine-pyrimidine metabolism,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ada, xdh, dpyd, pnp, hprt1, aprt, ada.2, mocos

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019254 - inborn disorder of purine or pyrimidine metabolism

MONDO:0019254 - inborn disorder of purine or 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)