| Approved symbol | IFT172 |
|---|---|
| Approved name | intraflagellar transport 172 |
| HGCN ID | HGNC:30391 |
| Previous symbols | |
| Inheritance | |
| OMIM | 607386 |
| Chromosome | 2p23.3 |
| Panel(s) |
NGS Cone-rod dystrophie en macula degeneratie NGS Intellectual disability NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Skeletdysplasie NGS Visus pakket Retinale genen |
