Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:17554325n
Noun Concept
NL
No term available
EN
13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Wikipedia
Relations
Sources
IS A
ziekte
EN
chromosomal deletion syndrome
HAS KIND
EN
Partial monosomy 13q

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