Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Multiple Epiphyseal Dysplasia via the MATN3 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Baylor Genetics United States | 1 | 354 |
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CGC Genetics Unilabs Portugal | 1 | 662 |
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Mendelics Brazil | 1 | 333 |
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Laboratorio de Genetica Clinica SL Spain | 1 | 152 |
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Laboratorio de Genetica Clinica SL Spain | 1 | 643 |
|
Spondylometaphyseal / spondyloepimetaphyseal dysplasia panel. 28-gene NGS panel. Genologica Medica Spain | 69 | 28 |
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Central skeletal dysplasias panel. NGS panel of 111 genes. Genologica Medica Spain | 258 | 111 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Epiphyseal dysplasia, multiple: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 7 | 7 |
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Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel Blueprint Genetics Finland | 2 | 308 |
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Comprehensive Skeletal Dysplasias and Disorders Panel Blueprint Genetics Finland | 1 | 246 |
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Skeletal Dysplasias Core Panel Blueprint Genetics Finland | 1 | 111 |
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EPIPHYSEAL DYSPLASIA, MULTIPLE (AUTOSOMAL DOMINANT) Laboratorio de Genetica Clinica SL Spain | 1 | 5 |
|
Spondylometaphyseal / Spondyloepi-(meta)-physeal Dysplasia Panel Blueprint Genetics Finland | 2 | 28 |
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Multiple epiphyseal dysplasia and pseudoachondroplasia Panel CeGaT GmbH Germany | 10 | 8 |
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Spondylometaphyseal dysplasia and Spondylo-epi-(meta)-physeal dysplasia Panel CeGaT GmbH Germany | 27 | 27 |
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Multiple epiphyseal dysplasia type 1 Bioarray Spain | 1 | 1 |
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Multiple epiphyseal dysplasia type 5 Bioarray Spain | 1 | 1 |
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CeGaT GmbH Germany | 2 | 1 |
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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.