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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
TPO - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Invitae Comprehensive Carrier Screen Labcorp Genetics (formerly Invitae) LabCorp United States | 886 | 547 |
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Congenital Hypothyroidism (Thyroid Dyshormonogenesis) via the TPO Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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Congenital Hypothyroidism and Thyroid Hormone Resistance Panel PreventionGenetics, part of Exact Sciences United States | 32 | 26 |
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Congenital Hypothyroidism Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 18 | 15 |
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Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes. Genologica Medica Spain | 42 | 21 |
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Asper Biogene Asper Biogene LLC Estonia | 85 | 64 |
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Hypothyroidism and Resistance to Thyroid Hormone NGS Panel Fulgent Genetics United States | 41 | 19 |
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Asper Biogene Asper Biogene LLC Estonia | 7 | 6 |
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Hypothyroidism and Thyroid Hormone Resistance Asper Biogene Asper Biogene LLC Estonia | 29 | 22 |
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Laboratorio de Genetica Clinica SL Spain | 9 | 10 |
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Familial thyroid dyshormonogenesis type 2A Bioarray Spain | 1 | 1 |
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Asper Biogene Asper Biogene LLC Estonia | 99 | 90 |
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Fulgent Genetics United States | 1 | 1 |
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Fulgent Genetics United States | 5128 | 4672 |
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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.