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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.
Glycogen Storage Disease Type IX - PHKG2 Related tests available.

PHKG2 Related Glycogen Storage Disease Type IX | Glycogen Storage Disease Type IXc | Glycogen Storage Disease Type VIII Autosomal Gamma Subunit | GSDIXc | Phosphorylase Kinase Deficiency Autosomal Liver | GSD9C | Glycogen Storage Disease IXc | PHK Deficiency testis/liver isoform

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Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing
Deletion/Duplication Analysis PHKG2 Deletion/Duplication Analysis
Test Code: 3983
Sequence & Deletion/Duplication Analysis PHKG2 Comprehensive - Sequence & Deletion/Duplication Analysis
Test Code: 3984
Sequence Analysis PHKG2 Sequence Analysis
Test Code: 3980
PHKG2 Sequence Analysis
Test Code: 3981

This test can only be performed if there is a previously identified familial mutation.
PHKG2 Sequence Analysis
Test Code: 3982

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.