| Approved symbol | DYNC2H1 |
|---|---|
| Approved name | dynein cytoplasmic 2 heavy chain 1 |
| HGCN ID | HGNC:2962 |
| Previous symbols | DNCH2 |
| Inheritance | |
| OMIM | 603297 |
| Chromosome | 11q22.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Disorder of sex development DSD NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Skeletal Dysplasia NGS Vision disorder CSNB |
