crouzon syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A craniosynostosis that involves premature fusion of certain skull bones. This early fusion prevents the skull from growing normally and affects the shape of the head and face. The disease is associated with mutations in the FGFR2 gene. (Human Disease Ontology, DOID_2339)
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1 genes associated with the crouzon syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2