| 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 dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
