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bn:02801001n
Noun Concept
Categories: Congenital disorders of musculoskeletal system, Genetic disorders with no OMIM, Syndromes
EN
Crouzonodermoskeletal syndrome  CAN  Crouzon-dermoskeletal syndrome  Crouzon syndrome-acanthosis nigricans syndrome  CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS
EN
Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull during development and a skin condition called acanthosis nigricans. Wikipedia
Definitions
Relations
Sources
EN
Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull during development and a skin condition called acanthosis nigricans. Wikipedia
autosomal dominant disease characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that has material basis in heterozygous missense mutation in the FGFR3 gene on chromosome 4p16 Wikidata
IS A
disease
rare disease
acanthosis nigricans
syndrome
bone disease
+1 relations
GENETIC ASSOCIATION
fibroblast growth factor receptor 3
Wikipedia
EN
Crouzonodermoskeletal syndrome
Wikidata
EN
Crouzonodermoskeletal syndrome
Wikipedia Redirections
EN
Crouzon syndrome with acanthosis nigricans
Wikidata Alias
EN
CAN, Crouzon-dermoskeletal syndrome, Crouzon syndrome-acanthosis nigricans syndrome, CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS, CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS; CAN, Crouzonodermoskeletal syndrome

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