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Results: 21 to 32 of 32

Tests names and labsConditionsGenes, analytes, and microbesMethods

(Mitochondrial) Optic Atrophy

MGZ Medical Genetics Center
Germany
27
  • C Sequence analysis of the entire coding region

Mitochondrial Depletion

MGZ Medical Genetics Center
Germany
312
  • C Sequence analysis of the entire coding region

DARS2

MGZ Medical Genetics Center
Germany
31
  • C Sequence analysis of the entire coding region

MGME1

MGZ Medical Genetics Center
Germany
31
  • C Sequence analysis of the entire coding region

Combined Oxidative Phosphorylation Deficiency 1

MGZ Medical Genetics Center
Germany
21
  • 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

Mitochondrial Respiratory Chain Complex IV Deficiency (Nuclear Genes)

MGZ Medical Genetics Center
Germany
28
  • C Sequence analysis of the entire coding region

Mitochondrial Disorders

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

Combined Oxidative Phosphorylation Deficiency 10

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

MERRF

MGZ Medical Genetics Center
Germany
42
  • C Sequence analysis of the entire coding region

MELAS, MT-TL1-Related

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

Mitochondrial DNA Deletion Syndromes

MGZ Medical Genetics Center
Germany
51
  • D Deletion/duplication analysis

Results: 21 to 32 of 32

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.