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Results: 1 to 20 of 54

Tests names and labsConditionsGenes, analytes, and microbesMethods

Genetic Renal Panel v8

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
2117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

CFB - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Inborn Errors of Immunity and Cytopenias Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
754562
  • D Deletion/duplication analysis

Invitae Complement Deficiency Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
3522
  • D Deletion/duplication analysis

Invitae Atypical Hemolytic Uremic Syndrome and Thrombotic Microangiopathies Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
2513
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemolytic uremic syndrome, atypical, susceptibility to, 4, 612924, Autosomal dominant; AHUS4 (Atypical hemolytic-uremic syndrome) (CFB gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hemolytic uremic syndrome, atypical, susceptibility to, 4, 612924, Autosomal dominant; AHUS4 (Atypical hemolytic-uremic syndrome) (CFB gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

RenalZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine
United States
525338
  • C Sequence analysis of the entire coding region

panel TTP (CFH, CFI, CFB, C3, MCP (CD46), MLPA CFH operon, ADAMTS13)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

panel Membranoproliferative Glomerulonephritis (CFH,CFI,CFB,C3,MCP(CD46),MLPA CFH operon,CFHR5)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CFB - membranoproliferative glomerulonephritis

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

panel Complement-Mediated Kidney Disease (CFH, CFI, CFB, C3, MCP (CD46), MLPA CFH operon)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
56
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

panel S. Pneumoniae HUS (CFH, CFI, CFB, C3, MCP (CD46), MLPA CFH operon)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
56
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CFB - C3-glomerulopathy

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

CFB - STEC-HUS

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

CFB - transplantation

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

CFB - complement nephropathy

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

CFB - atypical hemolytic uremic syndrome (aHUS)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

panel Transplantation (CFH, CFI, CFB, C3, MCP (CD46), MLPA CFH operon)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
56
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 54

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.