Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN.
|
27458560 |
2016 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
A functional variant in the CFI gene confers a high risk of age-related macular degeneration.
|
23685748 |
2013 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Complete factor I deficiency due to dysfunctional factor I with recurrent aseptic meningo-encephalitis.
|
24142231 |
2013 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
GeneticVariation
|
disease |
CLINVAR |
Complement factor I deficiency: a not so rare immune defect: characterization of new mutations and the first large gene deletion.
|
22710145 |
2012 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
|
20513133 |
2010 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome.
|
17106690 |
2007 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome.
|
16621965 |
2006 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome.
|
16621965 |
2006 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.
|
15173250 |
2004 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.
|
15173250 |
2004 |
Entrez Id: |
3426 |
Gene Symbol: |
CFI |
CFI
|
0.600 |
SusceptibilityMutation
|
disease |
CLINVAR |
|
|
|