Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:03137275n
Noun Concept
IT
No term available
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
Relations
Sources
IS A
osteocondrodisplasia
Sindrome di Pierre Robin
HEALTH SPECIALTY
genetica clinica

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