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Disease Ontology Browser
peroxisomal acyl-CoA oxidase deficiency (DOID:0050797)
Alliance: disease page
Synonyms: Peroxisomal acyl-coenzyme A oxidase
Alt IDs: OMIM:264470, MESH:C536662, NCI:C170437, ORDO:2971, UMLS_CUI:C1849678
Definition: A peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy that has_material_basis_in homozygous mutation in the ACOX1 gene on chromosome 17q25.1.

Disease References using Mouse Models (1)
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
12/10/2024
MGI 6.24 		The Jackson Laboratory