| Gene | Associated with APERT SYNDROME in | Link to HGNC | Cytogenetic band | Number of associated diseases | Associated diseases |
|---|---|---|---|---|---|
| FGFR2 | ClinVar, OMIM, HUMSAVAR | HGNC link | 10q26.13 | 11 | 101400, 101200, 149730, 614592, 123500, 207410, 613659, 123150, 609579, 101600, 123790 |