Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
CeGaT GmbH Germany | 37 | 59 |
|
Syndromes with immunodeficiency Panel CeGaT GmbH Germany | 33 | 38 |
|
Bone marrow failure syndromes Panel CeGaT GmbH Germany | 15 | 37 |
|
WAS Gene Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 2 | 1 |
|
Bioarray Spain | 1 | 1 |
|
Severe congenital neutropenia X-linked Bioarray Spain | 1 | 1 |
|
Wiskott-Aldrich syndrome, WAS sequencing Molecular Diagnostics Laboratory Seoul National University Hospital South Korea | 1 | 1 |
|
Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital India | 1 | 1 |
|
WAS Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 3 | 1 |
|
Fulgent Genetics United States | 2 | 1 |
|
Inherited Neutropenia panel by next-generation sequencing (NGS) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 39 | 40 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Fulgent Genetics United States | 32 | 15 |
|
Severe Congenital Neutropenia Sequential Panel FirmaLab United States | 1 | 5 |
|
MedGene Slovakia | 1 | 1 |
|
MedGene Slovakia | 1 | 1 |
|
Neutropenia, severe congenital MedGene Slovakia | 1 | 1 |
|
Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Neutropenia, severe congenital Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
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.