| Approved symbol | NPHP3 |
|---|---|
| Approved name | nephrocystin 3 |
| HGCN ID | HGNC:7907 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608002 |
| Chromosome | 3q22.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
