| Approved symbol | PRDM13 |
|---|---|
| Approved name | PR/SET domain 13 |
| HGCN ID | HGNC:13998 |
| Previous symbols | |
| Inheritance | |
| OMIM | 616741 |
| Chromosome | 6q16.2 |
| Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |
