| Approved symbol | PITPNM3 |
|---|---|
| Approved name | PITPNM family member 3 |
| HGCN ID | HGNC:21043 |
| Previous symbols | CORD5 |
| Inheritance | |
| OMIM | 608921 |
| Chromosome | 17p13.2-p13.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
