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Results: 1 to 20 of 116

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX10 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (FASTKD2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (PET100 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (APOPT1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (TACO1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (FASTKD2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (PET100 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX8A gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (APOPT1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX6B1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX14 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (SCO1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX10 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (TACO1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX20 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX6B1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX8A gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX14 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (COX20 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency, 220110, Autosomal recessive, Mitochondrial (Isolated cytochrome C oxidase deficiency) (SCO1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 116

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.