Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Stickler syndrome NGS panel - Recessive HNL Genomics Connective Tissue Gene Tests United States | 3 | 3 |
|
HNL Genomics Connective Tissue Gene Tests United States | 8 | 8 |
|
Stickler syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 8 |
|
Spondylo-Epi-Metaphyseal dysplasias NGS panel HNL Genomics Connective Tissue Gene Tests United States | 79 | 54 |
|
Spondylo-Epi-Metaphyseal dysplasias Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 79 | 54 |
|
Stickler syndrome Comprehensive panel - Recessive HNL Genomics Connective Tissue Gene Tests United States | 3 | 3 |
|
Vitreoretinopathy Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 23 | 19 |
|
Stickler syndrome Deletion / Duplication panel - Recessive HNL Genomics Connective Tissue Gene Tests United States | 3 | 3 |
|
Vitreoretinopathy Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 23 | 19 |
|
Stickler syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 8 |
|
Spondylo-Epi-Metaphyseal dysplasias Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 79 | 54 |
|
Comprehensive Vitreoretinopathy Panel PreventionGenetics, part of Exact Sciences United States | 26 | 21 |
|
Ehlers-Danlos Syndromes (EDS) Panel PreventionGenetics, part of Exact Sciences United States | 99 | 65 |
|
PreventionGenetics, part of Exact Sciences United States | 30 | 12 |
|
Stickler Syndrome Type II, Marshall Syndrome, and Fibrochondrogenesis via the COL11A1 Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
|
Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
|
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 39 | 13 |
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Cataract panel. NGS panel of 69 genes. Genologica Medica Spain | 146 | 69 |
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Spondylometaphyseal / spondyloepimetaphyseal dysplasia panel. 28-gene NGS panel. Genologica Medica Spain | 69 | 28 |
|
Marfan syndrome panel. 30-gene NGS panel. Genologica Medica Spain | 71 | 30 |
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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.