peroxisomal acyl-coa oxidase deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy. (Human Disease Ontology, DOID_0050797)
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1 genes associated with the peroxisomal acyl-coa oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ACOX1 acyl-CoA oxidase 1, palmitoyl