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Results: 41 to 56 of 56

Tests names and labsConditionsGenes, analytes, and microbesMethods

OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL (PEO)

Laboratorio de Genetica Clinica SL
Spain
54
  • C Sequence analysis of the entire coding region

Neuromuscular Disorders NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
233144
  • C Sequence analysis of the entire coding region

Mitochondrial Depletion NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3223
  • C Sequence analysis of the entire coding region

Rhabdomyolysis & Metabolic Myopathies NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
4647
  • C Sequence analysis of the entire coding region

Hereditary Ataxia

Asper Biogene Asper Biogene LLC
Estonia
180139
  • C Sequence analysis of the entire coding region

Progressive external ophthalmoplegia, autosomal dominant, 3

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing TWNK

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
173204
  • C Sequence analysis of the entire coding region

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37284
  • C Sequence analysis of the entire coding region

TWINKLE (PEO1/C10orf2) DNA Sequencing Test (Related to mtDNA depletion)

Athena Diagnostics
United States
21
  • C Sequence analysis of the entire coding region

Mitochondrial Hepatoencephalopathic Evaluation (POLG, DGUOK, MPV17, TWINKLE)

Athena Diagnostics
United States
94
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Ophthalmoplegia, progressive external 3

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Ophthalmoplegia, progressive external 3

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant 3

MGZ Medical Genetics Center
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TWNK/C10orf2-Related Mitochondrial Disorder

MGZ Medical Genetics Center
Germany
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 56 of 56

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.