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CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II

MedGen UID:
434347
•Concept ID:
CN071292
•
Disease or Syndrome

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

Recent clinical studies

Etiology

Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation.
Schejbel L, Schmidt IM, Kirchhoff M, Andersen CB, Marquart HV, Zipfel P, Garred P
Genes Immun 2011 Mar;12(2):90-9. Epub 2011 Jan 27 doi: 10.1038/gene.2010.63. PMID: 21270828

Supplemental Content

Table of contents

    Clinical resources

    Consumer resources

    Reviews

    Related information

    • ClinVar
      Related medical variations
    • GTR
      Related information in GTR
    • GTR(Clinical)
      Clinical tests in GTR
    • PubMed
      Related literature resources in PubMed

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