| Approved symbol | HMX1 |
|---|---|
| Approved name | H6 family homeobox 1 |
| HGCN ID | HGNC:5017 |
| Previous symbols | |
| Inheritance | |
| OMIM | 142992 |
| Chromosome | 4p16.1 |
| 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 |
