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Results: 1 to 20 of 67

Tests names and labsConditionsGenes, analytes, and microbesMethods

ACADVL Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

mtDNA Targeted Analysis: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

mtDNA Targeted Analysis with Heteroplasmy: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

Expanded 93 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

Leber Hereditary Optic Neuropathy (LHON)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
13
  • T Targeted variant analysis

Mitochondrial genome panel

Centogene AG - the Rare Disease Company
Germany
137
  • C Sequence analysis of the entire coding region

Aminoglycoside-Induced Hearing Loss Panel

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
73
  • T Targeted variant analysis

MT-ND1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

OtoSCOPE v9

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
288218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (MELAS)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
13
  • T Targeted variant analysis

Mitochondrial DNA-Associated Leigh Syndrome and NARP

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
126
  • T Targeted variant analysis

Mitochondrial Non Syndromic Hearing Loss and Deafness

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
14
  • T Targeted variant analysis

Leber hereditary optic atrophy(LHON): 3 mutations(G3460A, G11778A, T14484C)

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
13
  • T Targeted variant analysis

Leber's Hereditary Optic Neuropathy

Molecular Genetics Laboratory London Health Sciences Centre
Canada
13
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Genomic Unity® Hearing Loss Disorders Analysis

Variantyx, Inc.
United States
1318
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

Leber Hereditary Optic Neuropathy (LHON) - Targeted Testing for 3 Common Pathogenic Variants

PreventionGenetics, part of Exact Sciences
United States
13
  • T Targeted variant analysis

Mitochondrial Full Genome Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
2937
  • C Sequence analysis of the entire coding region

Congenital Lactic Acidosis Panel

Mayo Clinic Laboratories Mayo Clinic
United States
165
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGmito - Mitochondrial Genome Sequencing

PreventionGenetics, part of Exact Sciences
United States
1638
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 67

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.