Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:04515175n
Noun Concept
SYL
No term available
EN
type of disorder Wikidata
Relations
Sources
IS A
EN
disease
EN
phenotypic trait
HAS KIND
EN
genetic disease
EN
hereditary sensory and autonomic neuropathy
EN
hereditary CNS demyelinating disease
EN
collagen hereditary disease
EN
hereditary cavernous angioma
+1 relations
HAS INSTANCE
EN
lethal gene
EN
xanthochromism
EN
Aase syndrome
EN
hereditary cancer syndrome
EN
Madras motor neuron disease
+110 relations

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