CFHR2

complement factor H related 2
OMIM: 600889, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green CFHR2 in COVID-19 research Level 2: Viral research Version 1.146	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green IUIS Classification February 2018 IUIS Classification December 2019 GRID V2.0 Victorian Clinical Genetics Services IUIS Classification December 2019 IUIS Classification February 2018 Victorian Clinical Genetics Services GRID V2.0 Phenotypes Complement Deficiencies Age related macular degeneration Atypical hemolytic uremic syndrome susceptibility Older onset atypical hemolytic-uremic syndrome, disseminated neisserial infections
Green CFHR2 in Membranoproliferative glomerulonephritis including C3 glomerulopathy Level 2: Renal Version 3.8 Latest signed off version: v3.6 (30 Apr 2025) Component of the following Super Panels: Unexplained young onset end-stage renal disease	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes C3 glomerulopathy C3G Immune complex MPGN IC-MPGN Immune-complex-mediated MPGN Tags currently-ngs-unreportable gene-checked
Red CFHR2 in Primary immunodeficiency or monogenic inflammatory bowel disease Level 2: Immunology Version 8.78 Latest signed off version: v8.0 (30 Apr 2025)	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources IUIS Classification December 2019 IUIS Classification February 2018 Victorian Clinical Genetics Services Expert Review Red GRID V2.0 Phenotypes Older onset atypical hemolytic-uremic syndrome, disseminated neisserial infections Age related macular degeneration Complement Deficiencies Atypical hemolytic uremic syndrome susceptibility