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Disease Ontology Browser
Crouzon syndrome (DOID:2339)
Synonyms: Craniofacial Dysostosis; Crouzon's disease
Alt IDs: OMIM:123500, ICD10CM:Q75.1, MESH:D003394, NCI:C84653, UMLS_CUI:C0010273
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.

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory