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Results: 1 to 20 of 55

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

C3 - NGS including CNV analysis

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

CentoImmuno Panel

Centogene AG - the Rare Disease Company
Germany
323329
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical Hemolytic Uremic Syndrome (aHUS) Panel

Centogene AG - the Rare Disease Company
Germany
2325
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Inborn Errors of Immunity and Cytopenias Panel

Invitae
United States
754562
  • D Deletion/duplication analysis

Invitae Complement Deficiency Disorders Panel

Invitae
United States
3522
  • D Deletion/duplication analysis

Invitae Atypical Hemolytic Uremic Syndrome and Thrombotic Microangiopathies Panel

Invitae
United States
2513
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemolytic uremic syndrome, atypical, susceptibility to, 5, 612925, Autosomal dominant; AHUS5 (Atypical hemolytic-uremic syndrome) (C3 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, 5, 612925, Autosomal dominant; AHUS5 (Atypical hemolytic-uremic syndrome) (C3 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 Hospital
United States
527338
  • 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

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

C3 - atypical hemolytic uremic syndrome (aHUS)

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

C3 - S. Pneumoniae HUS

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

C3 - C3-glomerulonephritis

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

C3 - dense deposit disease

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

C3 - C3-glomerulopathy

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

Results: 1 to 20 of 55

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.