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bn:00616563n
Noun Concept
Categories: Genodermatoses, Rare syndromes, Cell surface receptor deficiencies, Hearing loss with craniofacial syndromes, Congenital disorders of musculoskeletal system
EN
Crouzon syndrome  Crouzon syndrone  Crouzon's Syndrome  CFD1  Courzon's syndrome
EN
Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Wikipedia
Definitions
Relations
Sources
EN
Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Wikipedia
Congenital disorder of the skull and face Wikidata
A genetic disorder that affects the first branchial (or pharyngeal) arch in a developing foetus, causing developmental problems. Wiktionary
IS A
rare disease
craniosynostosis
HAS KIND
Crouzonodermoskeletal syndrome
GENETIC ASSOCIATION
fibroblast growth factor receptor 2
HEALTH SPECIALTY
medical genetics
NAMED AFTER
Octave Crouzon
Wikipedia
EN
Crouzon syndrome
Wikidata
EN
Crouzon syndrone
Wiktionary
EN
Crouzon syndrome
Wikipedia Redirections
EN
Courzon's syndrome, Craniofacial dysarthrosis, craniofacial dysostosis, Crouzon's disease, Crouzon's Syndrome, Crouzon's syndrome, Crouzon disease, Crouzon Syndrome, Crouzons, Crouzon’s Syndrome, Petero Byakatonda
Wikidata Alias
EN
CFD1, Craniofacial Dysostosis, Craniofacial Dysostosis, Type 1, Craniofacial dysostosis type 1, Crouzon's disease, Crouzon craniofacial dysostosis, Crouzon disease, CROUZON SYNDROME

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