Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:03438050n
Noun Concept
PT
síndrome leopard
EN
Noonan syndrome with multiple lentigines which is part of a group called Ras/MAPK pathway syndromes, is a rare autosomal dominant, multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene. Wikipedia
Relations
Sources
IS A
doença rara
EN
RASopathy
GENETIC ASSOCIATION
BRAF
RAF1
PTPN11
HEALTH SPECIALTY
cardiologia
dermatologia
reumatologia
Wikipedia Translations
PT
síndrome leopard

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