Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01881431n
Noun Concept
FR
syndrome de Pitt-Hopkins
EN
Pitt–Hopkins syndrome is a rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent hyperventilation followed by apnea. Wikipedia
Relations
Sources
IS A
maladie rare
Maladie génétique
syndrome
GENETIC ASSOCIATION
TCF4
Wikidata
FR
syndrome de Pitt-Hopkins

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