Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:00059666n
Noun Concept
SYL
No term available
EN
Autosomal dominant disorder of connective tissue characterized by brittle bones that fracture easily WordNet 3.0
Relations
Sources
IS A
EN
autosomal dominant disease
EN
rare disease
EN
osteochondrodysplasia
HAS KIND
EN
Bruck syndrome
EN
Cole-Carpenter syndrome
EN
osteoporosis-pseudoglioma syndrome
GENETIC ASSOCIATION
EN
COL1A1
HEALTH SPECIALTY
EN
medical genetics

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