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Results: 1 to 10 of 10

Tests names and labsConditionsGenes, analytes, and microbesMethods

C4a deficiency, 614380, Autosomal recessive (Immunodeficiency due to a classical component pathway complement deficiency) (C4A 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

C4a deficiency, 614380, Autosomal recessive (Immunodeficiency due to a classical component pathway complement deficiency) (C4A 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

Genomic Unity® Renal Disorders Analysis

Variantyx, Inc.
United States
1425
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Immunodeficiencies - complement deficiencies (WES based NGS panel of 33 genes, including analysis of CNVs)

CGC Genetics Unilabs
Portugal
133
  • C Sequence analysis of the entire coding region

Immune Disorders Panel

CGC Genetics Unilabs
Portugal
1385
  • C Sequence analysis of the entire coding region

C4a deficiency: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Complement component C4 deficiency

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • 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

Complement deficiencies Panel

CeGaT GmbH
Germany
834
  • C Sequence analysis of the entire coding region

Results: 1 to 10 of 10

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