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Results: 21 to 40 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

MCP - transplantation

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

MCP - C3-glomerulonephritis

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

MCP - S. Pneumoniae HUS

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

panel STEC-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

panel Trombotic Microangiopathy (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 C3-Glomerulopathy (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 C3-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 Dense Deposit Disease (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

MCP - complement nephropathy

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

panel atypical 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

Invitae Primary Immunodeficiency Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
552424
  • D Deletion/duplication analysis

Inherited Renal Disorders Panel

Dhiti Omics Technologies Private Ltd
India
7257
  • C Sequence analysis of the entire coding region

Plugin system clutter panel. NGS panel of 75 genes.

Genologica Medica
Spain
7675
  • C Sequence analysis of the entire coding region

Hemolytic uremic syndrome panel. 9-gene NGS panel.

Genologica Medica
Spain
199
  • C Sequence analysis of the entire coding region

CD46 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

Hemolytic Uremic Syndrome

Asper Biogene Asper Biogene LLC
Estonia
1412
  • C Sequence analysis of the entire coding region

Complement Deficiency panel

Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
2833
  • C Sequence analysis of the entire coding region

Atypical Hemolytic Uremic Syndrome panel

Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
910
  • C Sequence analysis of the entire coding region

Hemolytic uremic syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
99
  • C Sequence analysis of the entire coding region

Results: 21 to 40 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.