SympGAN

Basic information of disease: C0003886

Disease name Arthrogryposis
Disease ID (CUI) C0003886
Disease alias
AMC - Arthrogryposis multiplex congenita
ARTHROGRYPOSIS
Amyoplasia Congenita
Amyoplasia congenita
Arthrogryposes
Arthrogryposes, Congenital Multiple
Arthrogryposis
Arthrogryposis (& [mul
Definition HPO2016_07_04: A non-progressive finding characterized by multiple joint contractures found throughout the body at birth. [HPO: probinson]
JABL99: Arthrogryposis marked by congenital contractures invol
External links
Related genes of disease: C0003886
Predicted genes of disease: C0003886
Candidate genes predicted by knowledge inference algorithm,
HypER, based on SympGAN knowledge graph.