Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hyperparathyroidism (WES based NGS panel of 11 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 11 |
|
Hypercalcemia (WES based NGS panel of 9 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 9 |
|
CGC Genetics Unilabs Portugal | 1 | 334 |
|
Hypocalciuric hypercalcemia, familial, type III (sequence analysis of AP2S1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Hyperparathyroidism panel. NGS panel of 13 genes. Genologica Medica Spain | 21 | 13 |
|
Bartter syndrome panel. 9-gene NGS panel. Genologica Medica Spain | 13 | 9 |
|
Hyperparathyroidism Cancer panel LifeLabs Genetics Canada | 1 | 7 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Xpanded Adult Movement Disorders Panel GeneDx United States | 5 | 473 |
|
Genetics Laboratory University of Oklahoma Health Sciences Center United States | 1 | 22 |
|
Nephrolithiasis and Nephrocalcinosis Panel GeneDx United States | 2 | 41 |
|
Nonsyndromic Intellectual Disability (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 19 | 560 |
|
GeneDx United States | 2 | 2592 |
|
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
|
Hypocalciuric hypercalcemia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 3 | 3 |
|
Abnormal Mineralization NGS Panel Fulgent Genetics United States | 77 | 30 |
|
Rare Kidney Stone Consortium And The Mayo Clinic Hyperoxaluria Center Mayo Clinic United States | 21 | 170 |
|
FAMILIAL HYPOCALCIURIC HYPERCALCEMIATYPE 3 Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Genetic Services Laboratory University of Chicago United States | 6 | 10 |
|
Blueprint Genetics Finland | 1 | 13 |
|
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