Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:05340819n
Noun Named Entity
JA
No term available
EN
An oculocutaneous albinism that has material basis in an autosomal recessive mutation of SLC45A2 on chromosome 5p13.2. Wikidata
Relations
Sources
IS A
EN
oculocutaneous albinism

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