Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
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Centogene AG - the Rare Disease Company Germany | 417 | 413 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Anterior Segment Dysgenesis Disorders Panel PreventionGenetics, part of Exact Sciences United States | 272 | 278 |
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PreventionGenetics, part of Exact Sciences United States | 157 | 171 |
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Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 47 |
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Cataract 3, Multiple Types (CTRCT3) via the CRYBB2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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PreventionGenetics, part of Exact Sciences United States | 44 | 41 |
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CGC Genetics Unilabs Portugal | 1 | 118 |
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CONGENITAL CATARACTS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 120 |
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Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 695 |
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Cataract panel. NGS panel of 69 genes. Genologica Medica Spain | 146 | 69 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Congenital Cataract Gene Sequencing Panel Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 49 |
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GeneDx United States | 1 | 85 |
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Cataract: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 38 | 37 |
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Congenital Cataracts NGS Panel Fulgent Genetics United States | 106 | 56 |
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Eye diseases comprehensive panel Asper Biogene Asper Biogene LLC Estonia | 367 | 291 |
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Asper Biogene Asper Biogene LLC Estonia | 45 | 44 |
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Blueprint Genetics Finland | 1 | 69 |
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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.