|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the peroxisomal acyl-coa oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
|ACOX1||acyl-CoA oxidase 1, palmitoyl|