| Approved symbol | FOXG1 |
|---|---|
| Approved name | forkhead box G1 |
| HGCN ID | HGNC:3811 |
| Previous symbols | FKHL2, FOXG1B, FKHL4, FKH2, FKHL1, FOXG1C, FKHL3, FOXG1A |
| Inheritance | |
| OMIM | 164874 |
| Chromosome | 14q12 |
| Panel(s) |
FOXG1 Analysis NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Movement disorders |
