rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
UNIPROT
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.
14978182
2004
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
UNIPROT
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
10577907
1999
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
UNIPROT
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
10762557
2000
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
UNIPROT
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
20513133
2010
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
UNIPROT
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
12960213
2003
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
UNIPROT
Genetic studies into inherited and sporadic hemolytic uremic syndrome.
9551389
1998
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
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
rs145975787
×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1
0.700
GeneticVariation
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