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Disease Ontology Browser
peroxisomal acyl-CoA oxidase deficiency (DOID:0050797)
Synonyms: Peroxisomal acyl-coenzyme A oxidase
Alt IDs: OMIM:264470, MESH:C536662, UMLS_CUI:C1849678
Definition: A peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/23/2017
MGI 6.09
The Jackson Laboratory