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Summary Literature (0)
DOID:2339 - Crouzon syndrome


Disease Ontology Definition: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.

Synonyms: Craniofacial Dysostosis; Crouzon's disease

Referenced OMIM:
OMIM:123500 - CROUZON SYNDROME

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : fgfr2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): craniosynostosis (is_a)


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