CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome
0.320 GeneticVariation disease ORPHANET The coding sequences and intron-exon boundaries of the complement factor H (CFH), complement factor I (CFI), Membrane Cofactor Protein (MCP), complement factor B (CFB) and C3 were sequenced in 33 women with a diagnosis of HELLP syndrome. 22594569 2012
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome
0.320 GeneticVariation disease BEFREE The coding sequences and intron-exon boundaries of the complement factor H (CFH), complement factor I (CFI), Membrane Cofactor Protein (MCP), complement factor B (CFB) and C3 were sequenced in 33 women with a diagnosis of HELLP syndrome. 22594569 2012
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome
0.320 Biomarker disease LHGDN Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome. 18658028 2008
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome
0.320 GeneticVariation disease ORPHANET Factor H, membrane cofactor protein, and factor I mutations in patients with hemolysis, elevated liver enzymes, and low platelet count syndrome. 18658028 2008