Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Neuropathy, Ataxia and Retinis pigmentosa (NARP) : T8993G mutation study Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 26 |
|
Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 4 | 27 |
|
LEBER HEREDITARY OPTIC NEUROPATHY (LHON) Laboratorio de Genetica Clinica SL Spain | 1 | 12 |
|
CeGaT GmbH Germany | 9 | 18 |
|
Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
|
Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
|
CGC Genetics Unilabs Portugal | 1 | 837 |
|
Leber optic atrophy (sequence analysis of MTND4 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Mitochondrial Diseases Panel (Nuclear and Mitochondrial DNA) Mendelics Brazil | 1 | 169 |
|
Dhiti Omics Technologies Private Ltd India | 28 | 37 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 1 | 3 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 37 |
|
Mitochondrial Complex I Subunits Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 1 | 4 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
Mitochondrial Genome NGS Panel Fulgent Genetics United States | 1 | 37 |
|
Leber hereditary optic neuropathy Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 1 | 1 |
|
Leber's hereditary optic neuropathy Centre for cellular and molecular biology Centre for Cellular and Molecular Biology India | 1 | 1 |
|
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