Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Comprehensive Nephrology Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 299 |
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Renal Stone/Electrolyte Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 82 | 71 |
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Invitae Expanded Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 693 | 388 |
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Centogene AG - the Rare Disease Company Germany | 498 | 498 |
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Centogene AG - the Rare Disease Company Germany | 499 | 499 |
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Invitae Renal Tubular Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 68 | 39 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 525 | 338 |
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Pseudohypoaldosteronism Type II Panel PreventionGenetics, part of Exact Sciences United States | 4 | 4 |
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Genomic Unity® Renal Disorders Analysis Variantyx, Inc. United States | 1 | 425 |
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Hypertension (WES based NGS panel of 15 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 15 |
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Pseudohypoaldosteronism (WES based NGS panel of 9 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 9 |
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CGC Genetics Unilabs Portugal | 1 | 334 |
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Pseudohypoaldosterolism panel. NGS panel of 10 genes. Genologica Medica Spain | 15 | 10 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Monogenic Hypertension Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 16 | 11 |
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Pseudohypoaldosteronism, type II: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 4 | 4 |
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Pseudohypoaldosteronism Type II: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 4 |
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PSEUDOHYPOALDOSTERONISM, TYPE 2 - GORDON SYNDROME (AUTOSOMAL DOMINANT) Laboratorio de Genetica Clinica SL Spain | 4 | 4 |
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Blueprint Genetics Finland | 1 | 10 |
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Nephrology Endocrinology and Electrolytes - panels MGZ Medical Genetics Center Germany | 5 | 117 |
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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.