| Approved symbol | NFIX |
|---|---|
| Approved name | nuclear factor I X |
| HGCN ID | HGNC:7788 |
| Previous symbols | |
| Inheritance | |
| OMIM | 164005 |
| Chromosome | 19p13.13 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia |
| Approved symbol | NFIX |
|---|---|
| Approved name | nuclear factor I X |
| HGCN ID | HGNC:7788 |
| Previous symbols | |
| Inheritance | |
| OMIM | 164005 |
| Chromosome | 19p13.13 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia |