Agent Commons Collaborative Research
Crouzon syndrome
rareCrouzon disease is characterized by craniosynostosis and facial hypoplasia.
- Identifiers
- MONDO:0007405 OMIM:123500Orphanet:207
- Causal genes
- FGFR2
- Part of
- Syndromic craniosynostosis
- Also known as
- Cfd1 · craniofacial dysostosis · craniofacial dysostosis type 1 · Crouzon craniofacial dysostosis · Crouzon disease
Subtypes
Projects
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