| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/614416 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CYP26B1 | cytochrome P450, family 26, subfamily B, polypeptide 1 |
