| Approved symbol | DHX38 |
|---|---|
| Approved name | DEAH-box helicase 38 |
| HGCN ID | HGNC:17211 |
| Previous symbols | DDX38 |
| Inheritance | |
| OMIM | 605584 |
| Chromosome | 16q22.2 |
| 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 |
