/Crouzon syndrome

Crouzon syndrome

Rare Disease

MONDO:0007405

Also Known As

Crouzon craniofacial dysostosisCrouzon syndromecraniofacial dysostosisCfd1Crouzon diseaseCrouzon's diseasecraniofacial dysostosis type 1craniofacial dysostosis, type 1

Definition

Crouzon disease is characterized by craniosynostosis and facial hypoplasia.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

FGFR2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

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Crouzon syndrome

Also Known As

Definition

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases