| Approved symbol | C1QTNF5 |
|---|---|
| Approved name | C1q and TNF related 5 |
| HGCN ID | HGNC:14344 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608752 |
| Chromosome | 11q23.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
