Clinical and research tests for CN257533 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 67

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFB9 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFS4 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFAF1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFA1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFS1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFS1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFA11 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFV2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (FOXRED1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFS3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFV1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFA11 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFAF3 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFB3 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFA1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFS2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (TMEM126B gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFAF2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (TMEM126B gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Mitochondrial complex I deficiency, 252010, Autosomal recessive, X-linked dominant, Mitochondrial (Isolated complex I deficiency) (NDUFAF4 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 67

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.