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Results: 1 to 16 of 16
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Mayo Clinic Laboratories Mayo Clinic United States | 1 | 51 |
|
Motor Neuron Disease Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 2 | 34 |
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ANXA11 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Amyotrophic Lateral Sclerosis (ALS) / Dementia Panel Centogene AG - the Rare Disease Company Germany | 64 | 66 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 72 | 33 |
|
Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) Panel PreventionGenetics, part of Exact Sciences United States | 45 | 38 |
|
Amyotrophic Lateral Sclerosis (ALS) Panel PreventionGenetics, part of Exact Sciences United States | 32 | 29 |
|
Amyotrophic Lateral Sclerosis / Motor Neuron Disease via the ANXA11 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Neurodegenerative panel _v.2.0 CGC Genetics Unilabs Portugal | 15 | 207 |
|
AMYOTROPHIC LATERAL SCLEROSIS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 57 |
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HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Frontotemporal dementia and/or Amyotrophic Lateral Sclerosis: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 30 | 30 |
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Invitae Amyotrophic Lateral Sclerosis Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 29 | 21 |
|
Fulgent Genetics United States | 1 | 1 |
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Results: 1 to 16 of 16
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.