Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
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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Johanson-Blizzard Syndrome via the UBR1 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Congenital Hypothyroidism and Thyroid Hormone Resistance Panel PreventionGenetics, part of Exact Sciences United States | 32 | 26 |
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GeneAware™ Expanded Panel (Female) Baylor Genetics United States | 1 | 422 |
|
GeneAware™ Expanded Panel (Male) Baylor Genetics United States | 1 | 382 |
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GeneAware™ Expanded Plus Panel (Female) Baylor Genetics United States | 1 | 446 |
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GeneAware™ Expanded Plus Panel (Male) Baylor Genetics United States | 1 | 401 |
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Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
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CGC Genetics Unilabs Portugal | 1 | 1307 |
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CGC Genetics Unilabs Portugal | 1 | 165 |
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CGC Genetics Unilabs Portugal | 1 | 129 |
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Congenital Heart Defects Panel CGC Genetics Unilabs Portugal | 1 | 208 |
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Johanson-Blizzard syndrome (sequence analysis of UBR1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Mendelics Brazil | 1 | 311 |
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Mendelics Brazil | 1 | 311 |
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Clinically Recognized Syndromes Panel Mendelics Brazil | 1 | 236 |
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ADAMS-OLIVER SYNDROME EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 8 |
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UBR1. Complete sequencing by NGS Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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CONGENITAL DIARRHEA SYNDROME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 65 |
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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.