craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614416
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Genes

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