C1QA, complement C1q A chain, 712

N. diseases: 88; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015230
Disease: Exanthema
Exanthema
0.310 Biomarker phenotype BEFREE In a case study of exploring the mechanism of rash, we find that HLAs, C1QA and APOA1 are the key gene players and thus can be potential targets (or biomarkers) in monitoring or countermining rashes. 30053268 2018
CUI: C0015230
Disease: Exanthema
Exanthema
0.310 Biomarker phenotype CTD_human Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family. 8840296 1996