| Approved symbol | LAMA1 |
|---|---|
| Approved name | laminin subunit alpha 1 |
| HGCN ID | HGNC:6481 |
| Previous symbols | LAMA |
| Inheritance | |
| OMIM | 150320 |
| Chromosome | 18p11.31 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
