Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
FAM111A Gene Gracile bone dysplasia NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
FAM111A Gene Kenny-Caffey syndrome type 2 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
FAM111A - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 99 | 101 |
|
Invitae Hypoparathyroidism Panel Invitae United States | 41 | 18 |
|
Invitae Comprehensive Neurometabolic Disorders Panel Invitae United States | 351 | 249 |
|
Invitae Skeletal Disorders Panel Invitae United States | 624 | 349 |
|
Kenny-Caffey syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 2 |
|
Kenny-Caffey syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 2 |
|
Kenny-Caffey syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 2 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
|
Kenny-Caffey syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 2 |
|
Kenny-Caffey syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 2 |
|
Kenny-Caffey syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 2 |
|
Invitae Treatable Neurometabolic Disorders Panel Invitae United States | 257 | 191 |
|
Kenny-Caffey Syndrome Type 2 via the FAM111A Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
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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.