Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01950612n
Noun Concept
SYL
No term available
EN
Mohr–Tranebjærg syndrome is a rare X-linked recessive syndrome also known as deafness–dystonia syndrome and caused by mutation in the TIMM8A gene. Wikipedia
Relations
Sources
IS A
EN
rare disease
EN
genetic disease
EN
mitochondrial disease
EN
X-linked intellectual disability
GENETIC ASSOCIATION
EN
TIMM8A

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