|
DOID:906 - peroxisomal disease
Disease Ontology Definition:An inherited metabolic disorder that involves peroxisome malfunction.
Synonyms: peroxisomal disorder
Xenbase Genes : pex10, pex3, acaa1, pex26, pex19, cat.2, pex1, ehhadh, pex14, mvk, acox1, pex5, amacr, hsd17b4, pex16,
MONDO:0019053 - peroxisomal disease |
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)