Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:00081745n
Noun Concept
SYL
No term available
EN
SCID in male children resulting from mutation of a gene that codes for a protein on the surface of T cells that allows them to develop a growth factor receptor WordNet 3.0
Relations
Sources
IS A
EN
severe combined immunodeficiency
EN
rare disease
GENETIC ASSOCIATION
EN
common gamma chain
HEALTH SPECIALTY
EN
hematology

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