| 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) |
| External Link | http://www.omim.org/entry/264470 |
| Similar Terms | |
| Downloads & Tools |
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 |
