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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Mayo Clinic Laboratories Mayo Clinic United States | 1 | 94 |
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Invitae Comprehensive Neurometabolic Disorders Panel Invitae United States | 351 | 249 |
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Phenylalanine Disorders Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 2 | 10 |
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Invitae Cerebral Palsy Spectrum Disorders Panel Invitae United States | 638 | 419 |
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qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
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Infantile Parkinsonism-Dystonia Panel PreventionGenetics, part of Exact Sciences United States | 6 | 6 |
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Invitae Treatable Neurometabolic Disorders Panel Invitae United States | 257 | 191 |
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Invitae Neurotransmitter Disorders Panel Invitae United States | 52 | 44 |
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CGC Genetics Unilabs Portugal | 1 | 837 |
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Movement diseases (WES based NGS panel of 931 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 10 | 930 |
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Neurodevelopmental and Movement Disorders Panel Mendelics Brazil | 2 | 121 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Congenital Hypotonia Xpanded Panel GeneDx United States | 10 | 1423 |
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GeneDx United States | 1 | 877 |
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GeneDx United States | 2 | 2592 |
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GeneDx United States | 1 | 1501 |
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Parkinsonism-dystonia, infantile: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
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Dopamine Metabolism Deficiency NGS Panel Fulgent Genetics United States | 19 | 16 |
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Neurotransmitter Metabolism Deficiency NGS Panel Fulgent Genetics United States | 85 | 101 |
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Mental retardation - different panels Institute of Human Genetics Cologne University Germany | 7 | 2536 |
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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.