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Results: 1 to 20 of 31

Tests names and labsConditionsGenes and analytesMethods

Mitochondrial genome panel

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

Leber optic atrophy

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leber optic atrophy

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial dysfunctions panel

Centogene AG - the Rare Disease Company
Germany
122
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Respiratory Chain Complex I Deficiency (Mitochondrial Genes)

(AC) Atlanta Center: Medical Neurogenetics, LLC.
United States
17
  • C Sequence analysis of the entire coding region

Mitochondrial Genome Sequence

Molecular Genetics Laboratory London Health Sciences Centre
Canada
2238
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MT-ND1, MT-ND6, MT-ND4. Detection of the mutations m.11778G>A, m.14484T>C and m.3460G>A by sequencing

Instituto de Medicina Genomica
Spain
13
  • E Sequence analysis of select exons

MTND1, MTND4, MTND6. Detection of the mutations m.11778G>A, m.14484T>C y m.3460G>A by sequencing

Instituto de Medicina Genomica
Spain
13
  • T Targeted variant analysis

Mitochondrial Disorders Panel (mtDNA Sequencing and Deletion/Duplication, 121 Nuclear Genes Sequencing, 119 Nuclear Genes Deletion/Duplication)

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
1158
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing MT-ND6

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Leber optic atrophy (sequence analysis of MTND6 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber's hereditary optic neuropathy

Molecular Diagnostics Division Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

mtDNA encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
1137
  • C Sequence analysis of the entire coding region

LHON, MT-ND1, MT-MD4, MT-ND6 Sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
13
  • C Sequence analysis of the entire coding region

DCM/LVNC Sequencing Panel

GeneDx
United States
237
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy Panel

GeneDx
United States
676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leber Hereditary Optic Neuropathy

MVZ Dortmund Dr. Eberhard and Partner
Germany
110
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Leber Hereditary Optic Neuropathy

MVZ Dortmund Dr. Eberhard and Partner
Germany
110
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

LHON mtDNA Evaluation

Athena Diagnostics Inc Quest Diagnostics
United States
13
  • T Targeted variant analysis

mtDNA complex 1 subunit sequencing

MitoMed Diagnostic Laboratory UCI
United States
17
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 31

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.