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DOID:0050797 - peroxisomal acyl-CoA oxidase deficiency
Disease Ontology Definition:A peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy.
Synonyms: Peroxisomal acyl-coenzyme A oxidase,
Echinobase Genes : acox1
MIM:264470 - peroxisomal acyl-coa oxidase deficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
peroxisomal disease (is_a)