Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Centogene AG - the Rare Disease Company Germany | 417 | 413 |
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Invitae Macular Dystrophy Panel Invitae United States | 66 | 36 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
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Stargardt Disease and Macular Dystrophies Amplexa Genetics Amplexa Genetics A/S Denmark | 2 | 23 |
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Molecular Vision Laboratory United States | 342 | 268 |
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Stargardt Disease (STGD) and Macular Dystrophies Panel PreventionGenetics, part of Exact Sciences United States | 35 | 28 |
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Sorsby Fundus Dystrophy via the TIMP3 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
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CGC Genetics Unilabs Portugal | 1 | 203 |
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CGC Genetics Unilabs Portugal | 1 | 306 |
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CGC Genetics Unilabs Portugal | 1 | 223 |
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Diseases of the posterior ocular segment (WES based NGS panel of 307 gene, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 307 |
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Stargardt disease and macular dystrophy (WES based NGS panel of 15 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 15 |
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Sorsby fundus dystrophy (deletion/duplication analysis of TIMP3 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Sorsby fundus dystrophy (sequence analysis of TIMP3 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Mendelics Brazil | 1 | 321 |
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Laboratorio de Genetica Clinica SL Spain | 1 | 49 |
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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.