Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Fibrochondrogenesis 1 NGS Test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
|
Skeletal dysplasia extended Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 26 | 19 |
|
Skeletal dysplasia core & extended NGS panel HNL Genomics Connective Tissue Gene Tests United States | 46 | 29 |
|
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 |
|
Skeletal dysplasia core & extended Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 46 | 29 |
|
Skeletal dysplasia extended Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 26 | 19 |
|
Skeletal dysplasia core & extended Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 46 | 29 |
|
Spondylo-Epi-Metaphyseal dysplasias Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 79 | 54 |
|
Skeletal dysplasia extended NGS panel HNL Genomics Connective Tissue Gene Tests United States | 26 | 19 |
|
Fibrochondrogenesis Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 2 | 2 |
|
Fibrochondrogenesis Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 2 | 2 |
|
HNL Genomics Connective Tissue Gene Tests United States | 2 | 2 |
|
Ehlers-Danlos Syndromes (EDS) Panel PreventionGenetics, part of Exact Sciences United States | 99 | 65 |
|
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 |
|
Cataract panel. NGS panel of 69 genes. Genologica Medica Spain | 146 | 69 |
|
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 |
|
Retinal dystrophy panel. 260 gene NGS panel. Genologica Medica Spain | 420 | 257 |
|
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.