CFHR2

complement factor H related 2
OMIM: 600889, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CFHR2 in COVID-19 research


Level 2: Viral research
Version 1.130

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

Level 3: Syndromes with prominent renal abnormalities
Level 2: Renal and urinary tract disorders
Version 2.26
Latest signed off version: v2.13 (16 Oct 2020)

Component of the following Super Panels:

  • Renal superpanel - broad
  • Renal superpanel - narrow
  • 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


    Version 2.573
    Latest signed off version: v2.1 (24 Feb 2020)

    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

    Red CFHR2 in Severe Paediatric Disorders


    Version 1.127

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Red
    • Expert list
    Phenotypes
    • {Hemolytic uremic syndrome, atypical, susceptibility to}, 235400
    • {Macular degeneration, age-related, reduced risk of}, 603075