Genetic involvement in craniosynostoses
| Gene | Chromosomal assignment | Disorder | OMIM | Ref |
|---|---|---|---|---|
| FGFR1 | 8p11 | Pfeiffer syndrome type 1 | 101600 | 8 |
| FGFR2 | 10q26 | Crouzon syndrome | 123500 | 15 |
| Apert syndrome | 101200 | 9 | ||
| Jackson-Weiss syndrome | 123510 | 16 | ||
| Pfeiffer syndrome type 2 and 3 | 101600 | 17, 18 | ||
| Saethre-Chotzen syndrome | 101400 | 7 | ||
| Beare-Stevenson syndrome with cutis gyrata | 123790 | 19 | ||
| FGFR3 | 4p16 | Crouzon syndrome with acanthosis nigricans | 100600 | 20 |
| Muenke syndrome | 602849 | 4, 3 |