Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:25337925n
Noun Named Entity
ES
No term available
EN
Hemochromatosis that has material basis in heterozygous mutation in the FTH1 gene on chromosome 11q12 Wikidata
Relations
Sources
IS A
enfermedad
enfermedad rara
enfermedad genética
hemocromatosis hereditaria
GENETIC ASSOCIATION
FTH1

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