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 involed in the disease crouzon syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
