OBO ID: DOID:2339
Term Name: Crouzon syndrome Search Ontology:
Synonyms:
  • Craniofacial Dysostosis
  • Crouzon's disease
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)
References:
Ontology: Human Disease   ( DOID:2339 )
Relationships
is a type of:
OTHER Crouzon syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FGFR2 Crouzon syndrome 123500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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