Disease: Arthrogryposis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		0.110 GeneticVariation disease BEFREE This study adds to the literature implicating defective axoglial function as a key cause of severe arthrogryposis multiplex congenita and suggests that GPR126 mutations should be investigated in individuals affected by this disorder. 26004201 2015
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		0.110 CausalMutation disease CLINVAR