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Results: 1 to 17 of 17
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Renal Stone/Electrolyte Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 82 | 71 |
|
Invitae Expanded Renal Disease Panel Invitae United States | 693 | 388 |
|
Centogene AG - the Rare Disease Company Germany | 669 | 688 |
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Centogene AG - the Rare Disease Company Germany | 247 | 262 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Invitae Progressive Renal Disease Panel Invitae United States | 310 | 195 |
|
Neurohypophyseal Diabetes Insipidus and Nephrogenic Diabetes Insipidus Panel PreventionGenetics, part of Exact Sciences United States | 4 | 3 |
|
Neurohypophyseal Diabetes Insipidus (NDI) via the AVP Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Diabetes insipidus panel. Panel NGS genes: AQP2, AVP, AVPR2. Genologica Medica Spain | 4 | 3 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
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Neurohypophyseal Diabetes Insipidus (AVP Single Gene Test) Fulgent Genetics United States | 1 | 1 |
|
Hereditary kidney disorders - different panels Institute of Human Genetics Cologne University Germany | 32 | 481 |
|
Neurohypophyseal Diabetes Insipidus, Sequencing AVP Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 1 | 1 |
|
Neurohypophyseal diabetes insipidus Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany | 1 | 1 |
|
Results: 1 to 17 of 17
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.