Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01758275n
Noun Concept
EL
No term available
EN
Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas. Wikipedia
Relations
Sources
IS A
ασθένεια
σπάνια πάθηση
πνευμονική στένωση βαλβίδας
GENETIC ASSOCIATION
EN
neurofibromin 1
HEALTH SPECIALTY
Ιατρική γενετική

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