×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
Biomarker
disease
GENOMICS_ENGLAND
Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.
26826462
2016
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
Biomarker
disease
GENOMICS_ENGLAND
Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN.
27458560
2016
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
20513133
2010
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.
14978182
2004
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
12960213
2003
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.
14583443
2003
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site.
11851332
2002
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
Biomarker
disease
GENOMICS_ENGLAND
Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.
11170895
2001
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
10762557
2000
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
10577907
1999
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
UNIPROT
Genetic studies into inherited and sporadic hemolytic uremic syndrome.
9551389
1998
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
CausalMutation
disease
CLINVAR
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
SusceptibilityMutation
disease
CLINVAR
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
0.600
GeneticVariation
disease
CLINVAR
×
Entrez Id:
3078
Gene Symbol:
CFHR1
CFHR1
0.300
Biomarker
disease
GENOMICS_ENGLAND
Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN.
27458560
2016
×
Entrez Id:
3078
Gene Symbol:
CFHR1
CFHR1
0.300
Biomarker
disease
GENOMICS_ENGLAND
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.
17367211
2007
×
Entrez Id:
10878
Gene Symbol:
CFHR3
CFHR3
0.300
Biomarker
disease
GENOMICS_ENGLAND
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.
17367211
2007
×
Entrez Id:
719
Gene Symbol:
C3AR1
C3AR1
0.100
GeneticVariation
disease
CLINVAR