Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Center for Genetics at Saint Francis Saint Francis Hospital United States | 1 | 1 |
|
Genetics Laboratory Shodair Children's Hospital United States | 1 | 1 |
|
HTT Gene Huntington disease NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Mayo Clinic Laboratories Mayo Clinic United States | 1 | 1 |
|
Molecular Pathology Laboratory University of Pennsylvania Health System United States | 1 | 1 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 1 | 1 |
|
Huntingtin (HTT) gene CAG triplet repeat test Neurogenetics Cyprus Institute of Neurology and Genetics Cyprus | 1 | 1 |
|
HTT - Repeat expansion analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Huntington disease, 143100, Autosomal dominant; HD (Huntington disease)(Repeat Analysis) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
|
Huntington Disease Analysis (by PCR) IU Genetic Testing Laboratories Indiana University School of Medicine United States | 1 | 1 |
|
Huntington disease presymptomatic testing Genetics Service Unit BRIC-National Institute of Biomedical Genomics India | 1 | 1 |
|
Huntington's disease: Triplet CAG Repeat expansion study Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
|
Huntington Disease via the HTT CAG Repeat Expansion PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Institute of Human Genetics Justus-Liebig University Germany | 3 | 1 |
|
Huntington Disease (HD) CAG Repeat Expansion ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 1 | 1 |
|
UCSF Molecular Diagnostics Laboratory University of California, San Francisco United States | 1 | 1 |
|
Molecular Diagnostic Laboratory Diagnostic Services, Shared Health Manitoba Canada | 1 | 1 |
|
Structural diseases of basal ganglia (WES based NGS panel of 72 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 73 |
|
Movement diseases (WES based NGS panel of 931 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 10 | 930 |
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