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Results: 1 to 20 of 97

Tests names and labsConditionsGenes, analytes, and microbesMethods

Autoinflammatory Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
182117
  • C Sequence analysis of the entire coding region

Early Onset IBD Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
163110
  • C Sequence analysis of the entire coding region

Bcell/Antibody Deficiency GenePanel

Mayo Clinic Laboratories Mayo Clinic
United States
7961
  • C Sequence analysis of the entire coding region

IKBKG Gene Ectodermal dysplasia, hypohidrotic, with immune deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

IKBKG Gene Immunodeficiency, isolated NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

IKBKG Gene Incontinentia pigmenti type 2 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

IKBKG Gene Invasive pneumococcal disease, recurrent isolated type 2 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

IKBKG Gene Atypical Mycobacterial infection NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

IKBKG - Sanger sequencing

Centogene AG - the Rare Disease Company
Germany
41
  • C Sequence analysis of the entire coding region

Mendelian Susceptibility to Mycobacterial Disease Panel

PreventionGenetics, part of Exact Sciences
United States
2917
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invasive pneumococcal disease, recurrent isolated, 2, 300640; IPD2 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG 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

Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG 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

Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG 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

Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Invasive pneumococcal disease, recurrent isolated, 2, 300640; IPD2 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (IKBKG 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

Immunodeficiency 33, 300636, X-linked recessive; IMD33 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Incontinentia pigmenti, 308300, X-linked dominant; IP (Incontinentia pigmenti) (IKBKG 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

Immunodeficiency, isolated, 300584 (X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Incontinentia pigmenti, 308300, X-linked dominant; IP (Incontinentia pigmenti) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Results: 1 to 20 of 97

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.