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Disease Ontology Browser
peroxisomal disease (DOID:906)
Alliance: disease page
Synonyms: peroxisomal disorder
Alt IDs: ICD10CM:E71.5, ICD9CM_2006:277.86, ICD9CM:277.86, MESH:D018901, NCI:C85005, UMLS_CUI:C0282528
Definition: An inherited metabolic disorder that involves peroxisome malfunction.

Disease References using Mouse Models (12)
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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Send questions and comments to User Support. 		last database update
05/30/2023
MGI 6.22 		The Jackson Laboratory