Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Parkinson Syndrome, autosomal recessive Panel CeGaT GmbH Germany | 9 | 11 |
|
Ataxia and differential diagnoses Panel CeGaT GmbH Germany | 172 | 204 |
|
CeGaT GmbH Germany | 42 | 48 |
|
Hereditary Degenerative Syndromes Panel CeGaT GmbH Germany | 28 | 49 |
|
Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel CeGaT GmbH Germany | 146 | 143 |
|
Selected Genetic Syndromes with Seizures Panel CeGaT GmbH Germany | 5 | 20 |
|
Fulgent Genetics United States | 3 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Parkinson-Alzheimer-Dementia NGS Panel Fulgent Genetics United States | 77 | 39 |
|
Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
|
Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Sequencing and Deletion/Duplication NBIA Testing Center Oregon Health & Science University United States | 5 | 1 |
|
Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Deletion/Duplication NBIA Testing Center Oregon Health & Science University United States | 5 | 1 |
|
Neuroaxonal dystrophy, infantile 1 MedGene Slovakia | 1 | 1 |
|
Neuroaxonal dystrophy, infantile 1 Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Sequencing and Deletion/Duplication Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University United States | 4 | 1 |
|
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