Filters
reset all| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Marfan Syndrome, Type 2 - TGFBR1 Gene Center for Genetics at Saint Francis Saint Francis Hospital United States | 5 | 1 |
|
Marfan Syndrome, Type 2 - TGFBR2 Gene Center for Genetics at Saint Francis Saint Francis Hospital United States | 5 | 1 |
|
Center for Genetics at Saint Francis Saint Francis Hospital United States | 3 | 1 |
|
Comprehensive Aortopathy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 54 | 48 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 23 | 12 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 8 | 1 |
|
GeneID Lab - Advanced Molecular Diagnostics United States | 73 | 61 |
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Health in Code Spain | 71 | 35 |
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Aortic Valvular Diseases Panel Health in Code Spain | 60 | 30 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
FBN1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 8 | 1 |
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PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
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Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences United States | 346 | 160 |
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Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States | 297 | 180 |
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Invitae Limb and Digital Malformations Panel Invitae United States | 356 | 177 |
|
Marfan Syndrome and Related Aortopathies Panel PreventionGenetics, part of Exact Sciences United States | 40 | 38 |
|
Congenital Diaphragmatic Hernia Panel PreventionGenetics, part of Exact Sciences United States | 116 | 65 |
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Marfan syndrome, type I / II Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 2 | 2 |
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Marfan syndrome and Loeys-Dietz syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 6 | 6 |
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Marfan syndrome, type I / II NGS panel HNL Genomics Connective Tissue Gene Tests United States | 2 | 2 |
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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.