skip to content »

Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
not shown on screen

Medical Genetics Test Services

View Custom Req   |    Tests in Custom Req: 0
Search Tests: (Search by disease, test name, gene name, test code, or keyword. Return to test index.)

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.

   Targeted Chromosomal Microarray Analysis - Prenatal - Amniotic Fluid
   Targeted Chromosomal Microarray Analysis - Prenatal - CVS
   Targeted mtDNA Analysis by Massively Parallel Sequencing (MitoNGSSM)
   Tay-Sachs Disease Carrier Testing (Serum) GeneReview
   Tay-Sachs Disease Carrier Testing (WBC) GeneReview
   TAZ - Related Disorders (BTHS, G4.5, XAP-2) OMIM
   T-Cell Clonality Screening by PCR
   TCIRG1-Related Autosomal Recessive Osteopetrosis OMIM
   Thrombophilia Mutation Panel OMIM
   Thymidine Determination - Plasma OMIM GeneReview
   TK2 - Related Disorders OMIM
   TMLHE Deficiency OMIM
   TOPORS-Related Retinitis Pigmentosa OMIM
   Total BluePrint Panel
   TP53 Somatic Mutation, Prognostic OMIM
   Transcobalamin II Deficiency (TCN2) OMIM
   Trifunctional Protein Deficiency Panel (HADHA & HADHB)
   Trio Whole Exome Sequencing
   Trio Whole Genome Sequencing
   TSHR-Related Disorders OMIM
   Tyrosinemia Type II (TAT) OMIM
   Tyrosinemia, Type 1 OMIM GeneReview