Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Genetics Laboratory Shodair Children's Hospital United States | 1 | 1 |
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HFE Targeted Mutation Analysis GENETIX Centro de Investigación en Genética Humana y Reproductiva Colombia | 1 | 1 |
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Diagnostic génotypique direct au locus HFE (hémochromatose héréditaire) Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL Canada | 1 | 1 |
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HFE-Associated Hereditary Hemochromatosis Molecular Genetics Laboratory London Health Sciences Centre Canada | 1 | 1 |
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HFE Targeted Mutation Analysis for Hemochromatosis Molecular Diagnostics Laboratory Duke University Health System United States | 1 | 1 |
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Molecular Genetics Laboratory London Health Sciences Centre Canada | 1 | 1 |
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HFE - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 6 | 1 |
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BMP2 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 3 | 1 |
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HFE - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 6 | 1 |
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BMP2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Invitae Iron Related Disorders Panel Invitae United States | 39 | 27 |
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Invitae Skeletal Disorders Panel Invitae United States | 624 | 349 |
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Invitae Limb and Digital Malformations Panel Invitae United States | 367 | 178 |
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Hemochromatosis, 235200, Autosomal recessive (Symptomatic form of hemochromatosis type 1) (MLPA) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Aventus Biolabs United States | 61 | 30 |
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Invitae Comprehensive Carrier Screen without X-linked Disorders Invitae United States | 228 | 279 |
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Invitae Comprehensive Carrier Screen Invitae United States | 247 | 301 |
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Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 20 | 46 |
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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.