| 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 dystrophy and macula degeneration NGS Hypothyroidism NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Skeletal Dysplasia NGS Vision disorder CSNB OTX2 Analysis |
