| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| External Link | https://www.disgenet.org/browser/0/1/0/C1849678 |
| Similar Terms | |
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3 genes associated with the disease Peroxisomal Acyl-Coa Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
