Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 Biomarker disease GENOMICS_ENGLAND A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor H. 26471127 2016
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 GeneticVariation disease UNIPROT Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. 20513133 2010
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 Biomarker disease GENOMICS_ENGLAND Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. 18796626 2008
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 GeneticVariation disease CLINVAR Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. 18796626 2008
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 GeneticVariation disease UNIPROT Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome. 18796626 2008
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 Biomarker disease GENOMICS_ENGLAND Molecular analysis of a novel hereditary C3 deficiency with systemic lupus erythematosus. 15781264 2005
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5
0.600 SusceptibilityMutation disease CLINVAR