| Approved symbol | FGD1 |
|---|---|
| Approved name | FYVE, RhoGEF and PH domain containing 1 |
| HGCN ID | HGNC:3663 |
| Previous symbols | FGDY |
| Inheritance | |
| OMIM | 300546 |
| Chromosome | Xp11.22 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Skeletal Dysplasia |
