Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
ARMC5 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 498 | 498 |
|
Centogene AG - the Rare Disease Company Germany | 499 | 499 |
|
Congenital Adrenal Hyperplasia (CAH) Panel Centogene AG - the Rare Disease Company Germany | 12 | 12 |
|
Centogene AG - the Rare Disease Company Germany | 247 | 262 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Primary Macronodular Adrenal Hyperplasia via the ARMC5 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 134 | 119 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
ACTH-independent macronodular adrenal hyperplasia 2 (sequence analysis of ARMC5 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Endocrine Neoplasia Panel (Expanded) Mendelics Brazil | 1 | 58 |
|
Hereditary Cancer Panel (Complete) Mendelics Brazil | 1 | 264 |
|
Mendelics Brazil | 1 | 8 |
|
Congenital adrenal hyperplasia panel. 9-gene NGS panel. Genologica Medica Spain | 14 | 9 |
|
ACTH-independent macronodular adrenal hyperplasia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
|
ACTH-independent macronodular adrenal hyperplasia 2 Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany | 1 | 1 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Nonsyndromic Intellectual Disability (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 19 | 560 |
|
Comprehensive Dementia (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 145 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
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