| Approved symbol | ADAMTS18 |
|---|---|
| Approved name | ADAM metallopeptidase with thrombospondin type 1 motif 18 |
| HGCN ID | HGNC:17110 |
| Previous symbols | ADAMTS21 |
| Inheritance | |
| OMIM | 607512 |
| Chromosome | 16q23.1 |
| 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 |
