WormBase Tree Display for DO_term: DOID:0050797
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| DOID:0050797 | Name | peroxisomal acyl-CoA oxidase deficiency | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| 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. | ||||
| Synonym | Exact | Peroxisomal acyl-coenzyme A oxidase | |||
| Parent | Is_a | DOID:906 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 264470 | |
| Attribute_of | Gene_by_orthology | WBGene00008167 | |||
| WBGene00008564 | |||||
| WBGene00008565 | |||||
| WBGene00008566 | |||||
| WBGene00008567 | |||||
| WBGene00010336 |
