Pfeiffer syndrome
Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis).
Associated Genes
| Gene Name | Chromosome number | BMRB Entries | PDB Entries |
|---|---|---|---|
| FGFR1 | 8 | BMRB Entries | PDB Entries |
| FGFR2 | 10 | PDB Entries |