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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
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Medical Genetics Test Services

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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.

   Fabry Disease OMIM GeneReview
   Factor V Leiden OMIM GeneReview
   FAM161A-Related Retinitis Pigmentosa OMIM
   FAM20C Related Disorders OMIM
   Familial Exudative Vitreoretinopathy (4 gene panel by NGS) GeneReview
   Familial Hypercholesterolemia OMIM
   Familial Thrombocytopenia with Propensity to Acute Myelogenous Leukemia OMIM
   FARS2 Related disorders OMIM
   FASTKD2 - Related Disorders OMIM
   Fatty Acid Oxidation Deficiency (22 gene panel by NGS)
   FH - Related Disorders OMIM
   FISH Analysis - Charcot-Marie-Tooth Neuropathy Type 1A OMIM GeneReview
   FISH Analysis - Chromosome X and Y Centromere Analysis
   FISH Analysis - Custom Familial FISH Studies
   FISH Analysis - DiGeorge/Velocardiofacial Syndrome Panel (22q and 10p) OMIM
   FISH Analysis - DiGeorge/Velocardiofacial Syndrome Type I (22q) OMIM GeneReview
   FISH Analysis - Hereditary Neuropathy with Liability to Pressure Palsies OMIM GeneReview
   FISH Analysis - Langer-Giedion Syndrome Panel (EXT1 and TRPS1) OMIM
   FISH Analysis - Neurofibromatosis Type I OMIM GeneReview
   FISH Analysis - Prenatal Aneuploidy
   FISH Analysis - SRY Related Phenotypes OMIM GeneReview
   FLT3 Mutation Analysis OMIM
   FMR1 - Related Disorders OMIM GeneReview
   Focal Dermal Hypoplasia OMIM GeneReview
   FOXF1 - Related Disorders OMIM
   Friedreich Ataxia (FRDA) OMIM GeneReview
   Fructose 1,6 Bisphosphatase Deficiency (FBP1) OMIM
   FSCN2-Related Retinitis Pigmentosa OMIM