CFHR3

complement factor H related 3
OMIM: 605336, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green CFHR3 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 CFHR3 in Atypical haemolytic uraemic syndrome 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 Literature UKGTN Phenotypes Hemolytic uremic syndrome, atypical, susceptibility to 235400
Red CFHR3 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 Expert Review Red IUIS Classification December 2019 IUIS Classification February 2018 Victorian Clinical Genetics Services GRID V2.0 Phenotypes Older onset atypical hemolytic-uremic syndrome, disseminated neisserial infections Age related macular degeneration Complement Deficiencies Atypical hemolytic uremic syndrome susceptibility