Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Spinal Muscular Atrophy NGS Panel Fulgent Genetics United States | 93 | 29 |
|
Riboflavin Transporter Deficiency Neuronopathy NGS Panel Fulgent Genetics United States | 48 | 2 |
|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Fulgent Genetics United States | 505 | 132 |
|
Fulgent Genetics United States | 85 | 7 |
|
Fulgent Genetics United States | 186 | 61 |
|
Osteogenesis Imperfecta and Decreased Bone Density NGS Panel Fulgent Genetics United States | 111 | 32 |
|
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
|
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States | 450 | 128 |
|
Neuronal Migration Disorders NGS Panel Fulgent Genetics United States | 392 | 83 |
|
Noonan and RASopathies NGS Panel Fulgent Genetics United States | 235 | 26 |
|
Paroxysmal Extreme Pain Disorder NGS Panel Fulgent Genetics United States | 185 | 53 |
|
Kaufman Oculocerebrofacial Syndrome (UBE3B Single Gene Test) Fulgent Genetics United States | 52 | 1 |
|
Fulgent Genetics United States | 533 | 149 |
|
Congenital Adrenal Hyperplasia NGS Panel Fulgent Genetics United States | 32 | 8 |
|
Congenital Heart Defect NGS Panel Fulgent Genetics United States | 377 | 114 |
|
Cerebral Cortical Malformation NGS Panel Fulgent Genetics United States | 210 | 42 |
|
Fulgent Genetics United States | 49 | 1 |
|
Fulgent Genetics United States | 48 | 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.