| Approved symbol | PEX13 |
|---|---|
| Approved name | peroxisomal biogenesis factor 13 |
| HGCN ID | HGNC:8855 |
| Previous symbols | |
| Inheritance | |
| OMIM | 601789 |
| Chromosome | 2p15 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders NGS White matter disease |
