Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 713
Gene Symbol: C1QB
C1QB
CUI: C3150902
Disease: C1q DEFICIENCY
C1q DEFICIENCY 		0.710 GeneticVariation UNIPROT Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects. 9476130

1997
Entrez Id: 714
Gene Symbol: C1QC
C1QC
CUI: C3150902
Disease: C1q DEFICIENCY
C1q DEFICIENCY 		0.700 GeneticVariation UNIPROT Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families. 8630118

1996