| Approved symbol | OTX2 |
|---|---|
| Approved name | orthodenticle homeobox 2 |
| HGCN ID | HGNC:8522 |
| Previous symbols | |
| Inheritance | |
| OMIM | 600037 |
| Chromosome | 14q22.3 |
| Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Intellectual disability NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Retinitis pigmentosa NGS Visus pakket Retinale genen NGS Volledig Hypothyreoidie panel OTX2 Analysis |
