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Results: 1 to 20 of 20
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 243 | 238 |
|
GNRH1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 498 | 498 |
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Centogene AG - the Rare Disease Company Germany | 499 | 499 |
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Invitae Hypogonadotropic Hypogonadism Panel Invitae United States | 67 | 46 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Hypogonadotropic Hypogonadism/Kallmann Panel PreventionGenetics, part of Exact Sciences United States | 35 | 38 |
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Differences of Sex Development (DSD) Panel PreventionGenetics, part of Exact Sciences United States | 149 | 158 |
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Differences of Sex Development (DSD) and Infertility Panel PreventionGenetics, part of Exact Sciences United States | 223 | 238 |
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PreventionGenetics, part of Exact Sciences United States | 128 | 139 |
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PreventionGenetics, part of Exact Sciences United States | 96 | 105 |
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Idiopathic Hypogonadotropic Hypogonadism (IHH) via the GNRH1 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Fulgent Genetics United States | 79 | 45 |
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Fulgent Genetics United States | 92 | 56 |
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Fulgent Genetics United States | 76 | 41 |
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Hypogonadotropic Hypogonadism/Kallmann Panel Genetic Services Laboratory University of Chicago United States | 14 | 42 |
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Fulgent Genetics United States | 2 | 1 |
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Hypogonadotropic Hypogonadism (HH) and Related Disorders NGS Panel Fulgent Genetics United States | 22 | 13 |
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Fulgent Genetics United States | 5129 | 4672 |
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Fulgent Genetics United States | 28 | 19 |
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Results: 1 to 20 of 20
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.