|OBO ID: DOID:2339|
|Term Name:||Crouzon syndrome||Search 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. (4)|
|Ontology:||Human Disease (DOID:2339)|
|is a type of:||
OTHER Crouzon syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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