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bn:00616563n
Noun Concept
SYL
No term available
EN
Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
craniosynostosis
HAS KIND
EN
Crouzonodermoskeletal syndrome
GENETIC ASSOCIATION
EN
fibroblast growth factor receptor 2
HEALTH SPECIALTY
EN
medical genetics
NAMED AFTER
EN
Octave Crouzon

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