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Gene Information
Gene symbol: CFHR3
Gene name: complement factor H-related 3
HGNC ID: 16980
Synonyms: FHR-3, HLF4, FHR3, DOWN16
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | CFH | 1 hits |
| 2 | CFHR1 | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 19388158 | Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS. |
| 2 | 19388158 | Thus CFHR1 and CFHR3 proteins, and likely also the other members of this gene family are linked to human diseases. |
| 3 | 19388158 | We here summarize the current knowledge about the role or association of CFHR1 and CFHR3 in the human diseases HUS and AMD. |
| 4 | 19388158 | Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS. |
| 5 | 19388158 | Thus CFHR1 and CFHR3 proteins, and likely also the other members of this gene family are linked to human diseases. |
| 6 | 19388158 | We here summarize the current knowledge about the role or association of CFHR1 and CFHR3 in the human diseases HUS and AMD. |
| 7 | 19388158 | Homozygous chromosomal deletion of a genomic 84 kb, chromosomal fragment which includes the genes CFHR1/CFHR3 is a risk factor for hemolytic uremic syndrome (HUS) at young age and is predominantly associated with the generation of autoantibodies to CFH, leading to a specific type of HUS, called DEAP (deficiency of CFHR and autoantibody positive)-HUS. |
| 8 | 19388158 | Thus CFHR1 and CFHR3 proteins, and likely also the other members of this gene family are linked to human diseases. |
| 9 | 19388158 | We here summarize the current knowledge about the role or association of CFHR1 and CFHR3 in the human diseases HUS and AMD. |
| 10 | 25941307 | We present a child with a hybrid CFH/CFHR3 gene who, having had multiple disease relapses despite optimal treatment with plasma exchange, commenced eculizumab therapy in August 2010. |