Crouzon syndrome
Crouzon syndrome
Definition
Crouzon disease is characterized by craniosynostosis and facial hypoplasia.
Also known as craniofacial dysostosis, Crouzon craniofacial dysostosis, Crouzon syndrome — per MONDO
Also identified as
- DOID 2339 per MONDO
- MESH D003394 per MONDO
- NCIT C84653 per MONDO
- OMIM 123500 per MONDO
- Orphanet 207 per MONDO
- SCTID 28861008 per MONDO
- UMLS C0010273 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Bone element | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Bone element | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Connective tissue | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |