Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:01245442n
Noun Concept
Categories: Rare diseases, Congenital disorders, long volume value, Genetic disorders with OMIM but no gene, Autosomal recessive disorders
EN
fibrochondrogenesis  FBCG1  FIBROCHONDROGENESIS 1  FIBROCHONDROGENESIS 1; FBCG1  Fibrochondrogenesis type 1
EN
Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues. Wikipedia
Definitions
Relations
Sources
EN
Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues. Wikipedia
Human disease Wikidata
IS A
rare disease
osteochondrodysplasia
GENETIC ASSOCIATION
COL11A2
Collagen, type XI, alpha 1
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
fibrochondrogenesis
Wikidata
EN
fibrochondrogenesis
Wikidata Alias
EN
FBCG1, FIBROCHONDROGENESIS 1, FIBROCHONDROGENESIS 1; FBCG1, Fibrochondrogenesis type 1

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