Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01611654n
Noun Concept
NL
No term available
EN
Hyaluronidase deficiency is a condition caused by mutations in the HYAL1 gene, and is characterized by multiple soft-tissue masses. Wikipedia
Relations
Sources
IS A
zeldzame ziekte
Mucopolysaccharidosen
GENETIC ASSOCIATION
HYAL1
MODE OF INHERITANCE
dominantie

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