Crouzon syndrone (Q17116): Difference between revisions
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Created claim: instance of (P2): developmental defect during embryogenesis (Q13937) |
Created claim: instance of (P2): designated intractable/rare diseases (Q12701) |
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Revision as of 20:24, 29 December 2023
Congenital disorder of the skull and face
- Craniofacial Dysostosis
- Crouzon's disease
- Craniofacial dysostosis type 1
- CROUZON SYNDROME
- CFD1
- Craniofacial Dysostosis, Type 1
- Crouzon craniofacial dysostosis
- Crouzon disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Crouzon syndrone |
Congenital disorder of the skull and face |
|