Mitochondrial Diseases Panel (Nuclear and Mitochondrial DNA)
Clinical Genetic Test
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offered by
GTR Test Accession: Help GTR000604165.1
MITOCHONDRIAL DISEASE
Registered in GTR: 2023-03-17
Last annual review date for the lab: 2024-03-14 LinkOut
At a Glance
Diagnosis
Mitochondrial disease
AARS2 (6p21.1); ACAD9 (3q21.3); AIFM1 (Xq26.1); ATP5F1A (18q21.1); ATP5F1E (20q13.32) more...
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Not provided
Not provided
Ordering Information
Offered by: Help
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 169
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Accuracy >= 97.5%
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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