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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
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Medical Genetics Test Details

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The American Medical Association (AMA) Current Procedural Terminology (CPT) codes and Healthcare Common Procedure Coding System (HCPCS) codes listed, are provided for informational purposes only. The codes reflect our interpretation of CPT/HCPCS coding requirements based upon AMA guidelines published annually. CPT/HCPCS codes are provided only as guidance to assist clients with billing. Baylor Genetics strongly recommends that clients confirm CPT/HCPCS codes with their Medicare Administrative Contractor (MAC) or other payer being billed, as requirements may differ. CPT coding is the sole responsibility of the billing party. Baylor Genetics assumes no responsibility for billing errors due to reliance on the CPT codes listed. Please direct any questions regarding CPT coding to the payer being billed.
COX10 - Related Disorders tests available.

Leigh Syndrome (nuclear DNA mutation) | Leigh Disease | Leigh Syndrome Due to Cytochrome c Oxidase Deficiency | Mitochondrial Respiratory Chain Complex IV Deficiency (nuclear genes) | Complex IV (COX) Deficiency | COX Deficiency (nuclear genes) | Cytochrome c Oxidase Deficiency

(Click the blue dot to view test details. Red dot = current test.)
Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing
Deletion/Duplication Analysis COX10 Deletion/Duplication Analysis
Test Code: 3103
Sequence & Deletion/Duplication Analysis COX10 Comprehensive - Sequence & Deletion/Duplication Analysis
Test Code: 3104
Sequence Analysis COX10 Sequence Analysis
Test Code: 3100
COX10 Sequence Analysis
Test Code: 3101

This test can only be performed if there is a previously identified familial mutation.
COX10 Sequence Analysis
Test Code: 3102

We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363.