Crouzon syndrone (Q17116): Difference between revisions

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Created claim: exact match (P409): http://purl.obolibrary.org/obo/HP_0004439
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_207
 
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_207 / rank
 
Normal rank

Latest revision as of 20:48, 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
  • Craniofacial Dysostosis
  • Crouzon's disease
  • Craniofacial dysostosis type 1
  • CROUZON SYNDROME
  • CFD1
  • Craniofacial Dysostosis, Type 1
  • Crouzon craniofacial dysostosis
  • Crouzon disease

Statements