| Approved symbol | SAMD11 |
|---|---|
| Approved name | sterile alpha motif domain containing 11 |
| HGCN ID | HGNC:28706 |
| Previous symbols | |
| Inheritance | |
| OMIM | 616765 |
| Chromosome | 1p36.33 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
