Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:03137275n
Noun Concept
Categories: Congenital disorders, Autosomal recessive disorders, Syndromes with cleft lip and/or palate, Syndromes affecting the jaw, Syndromes affecting hearing
EN
Weissenbacher-Zweymuller syndrome  Weissenbacher–Zweymüller syndrome  Piere-Robin syndrome  Pierre Robin Malformation  Weissenbacher-Zweymueller syndrome
EN
Weissenbacher–Zweymuller syndrome, also called Pierre-Robin syndrome with fetal chondrodysplasia, is an autosomal recessive congenital disorder, linked to mutations in the COL11A2 gene, which codes for the α2 strand of collagen type XI. Wikipedia
Definitions
Relations
Sources
EN
Weissenbacher–Zweymuller syndrome, also called Pierre-Robin syndrome with fetal chondrodysplasia, is an autosomal recessive congenital disorder, linked to mutations in the COL11A2 gene, which codes for the α2 strand of collagen type XI. Wikipedia
Human disease Wikidata
IS A
osteochondrodysplasia
Pierre Robin sequence
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
Weissenbacher–Zweymüller syndrome
Wikidata
EN
Weissenbacher-Zweymuller syndrome
Wikipedia Redirections
EN
Weissenbacher-Zweymueller syndrome, Weissenbacher-Zweymuller syndrome, Weissenbacher-Zweymüller syndrome, Weissenbacher Zweymuller syndrome, Weissenbacher–Zweymuller syndrome, WZS
Wikidata Alias
EN
Piere-Robin syndrome, Pierre Robin Malformation

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License