Approved symbol | INVS |
---|---|
Approved name | inversin |
HGCN ID | HGNC:17870 |
Previous symbols | NPHP2 |
Inheritance | |
OMIM | 243305 |
Chromosome | 9q31.1 |
Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |