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Disease Ontology Browser
purine-pyrimidine metabolic disorder (DOID:653)
Alliance: disease page
Synonyms: inborn errors of purine-pyrimidine metabolism
Alt IDs: ICD10CM:E79.8, ICD9CM:277.2, UMLS_CUI:C0029595
Definition: An inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory