Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:02017720n
Noun Concept
AR
No term available
EN
Hereditary inclusion body myopathies are a group of rare genetic disorders which have different symptoms. Wikipedia
Relations
Sources
IS A
مرض
اعتلال عضلي
HAS KIND
EN
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
EN
distal myopathy, Nonaka type

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