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Results: 1 to 16 of 16 (representing 10 labs)

Tests names and labsConditionsGenes and analytesMethods

Cardiomyopathy, infantile hypertrophic, MT-ATP8 related

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

Cardiomyopathy, apical hypertrophic, and neuropathy, MT-ATP8 related

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

Mitochondrial genome panel

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

Mitochondrial Genome Sequence

Molecular Genetics Laboratory London Health Sciences Centre
Canada
2238
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • 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 and Genomics
United States
1157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Genome NGS Panel

Fulgent Genetics
United States
237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Mitochondrial Metabolic Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
4196
  • C Sequence analysis of the entire coding region

mtDNA encoded Mitochondriopathies Panel

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

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37302
  • C Sequence analysis of the entire coding region

Mitochondrial DNA-Associated Leigh Syndrome and NARP

Medizinisch Genetisches Zentrum München MGZ München
Germany
12
  • C Sequence analysis of the entire coding region

Mitochondrial Cardiomyopathy - Sanger

Medizinisch Genetisches Zentrum München MGZ München
Germany
112
  • C Sequence analysis of the entire coding region

Leigh Syndrome (nuclear DNA mutation)

Medizinisch Genetisches Zentrum München MGZ München
Germany
125
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear Type 2

Medizinisch Genetisches Zentrum München MGZ München
Germany
12
  • C Sequence analysis of the entire coding region

mtSEEK® Mitochondrial Genome Sequencing with Deletion Detection and Heteroplasmy Analysis

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
1336
  • C Sequence analysis of the entire coding region

Mitochondrial Disorders (mtDNA) Sequencing

ARUP Laboratories, Molecular Genetics and Genomics
United States
133
  • C Sequence analysis of the entire coding region

Mitochondrial diseases

Center for Human Genetics, Inc
United States
114
  • C Sequence analysis of the entire coding region

Results: 1 to 16 of 16

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.

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