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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.



   PCDH15 Related Disorders OMIM
   PCDH19 - Related X-Linked Female-Limited Epilepsy w/MR OMIM
   PDE6B-Related Retinitis Pigmentosa OMIM
   PDH & Mitochondrial Respiratory Chain Complex V Deficiency (9 nuclear gene panel by NGS)
   PDHA1 - Related Disorders OMIM
   PD-L1 22C3 IHC for NSCLC by Immunohistochemistry with Interpretation, Pembrolizumab (KEYTRUDA)
   PD-L1 22C3 IHC with Combined Positive Score (CPS) Interpretation, pembrolizumab (KEYTRUDA)
   PD-L1 28-8 pharmDx by Immunohistochemistry with Interpretation, nivolumab (OPDIVO)
   Pelizaeus-Merzbacher-Like Disease OMIM
   Peroxisomal Disorders (22 gene panel by NGS) GeneReview
   PGM3 Related Disorders (PGM3) OMIM
   Phenylalanine Hydroxylase Deficiency (PAH) OMIM GeneReview
   Phenylbutyrate Metabolite Analysis
   PHEO and PGL Syndrome Panel (SDHB, SDHC, & SDHD) OMIM GeneReview
   PLP1 - Related Disorders OMIM GeneReview
   PML-RARA Translocation, t(15;17) by RT-PCR, Quantitative
   POLG - Related Disorders (POLG1, POLGA) OMIM GeneReview
   POLG2 - Related Disorders OMIM
   Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract Disorder (ABHD12) OMIM
   Pontocerebellar Hypoplasia Type 6 (RARS2) OMIM
   Prader-Willi Syndrome OMIM GeneReview
   Prader-Willi-like Syndrome; Intellectual Disability; Autism (MAGEL2)
   Prenatal Trio Whole Exome Sequencing
   PreSeek Non-invasive Prenatal Gene Sequencing Screen
   Primary Open Angle Glaucoma (2 gene panel by NGS)
   Proband Whole Exome Sequencing
   Proband Whole Exome Sequencing Plus CMA
   Proband Whole Genome Sequencing
   Progressive External Ophthalmoplegia - PEO Panel (10 gene panel by NGS)
   PROM1-Related Retinitis Pigmentosa OMIM
   Propionic Acidemia - PCCA Related OMIM GeneReview
   Propionic Acidemia - PCCB Related OMIM GeneReview
   Propionic Acidemia Panel (PCCA & PCCB)
   Prothrombin Mutation Panel OMIM GeneReview
   Proximal Urea Cycle Disorders (3 gene panel by NGS) GeneReview
   PRPF31-Related Retinitis Pigmentosa OMIM
   PRPH2-Related Retinitis Pigmentosa OMIM
   PTEN - Related Disorders OMIM
   PTPN11 - Related Disorders OMIM
   Pycnodysostosis (CTSK) OMIM
   Pyridoxine-Dependent Seizures OMIM GeneReview
   Pyruvate Carboxylase Deficiency (PC) OMIM GeneReview
   Pyruvate Dehydrogenase Deficiency (PDHB) OMIM
   Pyruvate Dehydrogenase E2 Deficiency (DLAT) OMIM
   Pyruvate Dehydrogenase E3-Binding Protein (Component X) Deficiency (PDHX) OMIM
   Pyruvate Dehydrogenase Phosphatase Deficiency (PDP1) OMIM