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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.

   Paraganglioma/Pheochromocytoma (TMEM127) OMIM
   PAX6 Related Disorders OMIM
   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
   PEPCK deficiency, mitochondrial (PCK2) OMIM
   Peroxisomal acyl-CoA oxidase deficiency (ACOX1) OMIM
   Peroxisomal Disorders (22 gene panel by NGS) GeneReview
   Peroxisome Biogenesis Disorder 1 (PEX1) OMIM
   Peroxisome Biogenesis Disorder 10A (Zellweger) (PEX3) OMIM
   Peroxisome Biogenesis Disorder 11 (PEX13) OMIM
   Peroxisome Biogenesis Disorder 12A (Zellweger) (PEX19) OMIM
   Peroxisome Biogenesis Disorder 13A (Zellweger) (PEX14) OMIM
   Peroxisome Biogenesis Disorder 14B (PEX11B) OMIM
   Peroxisome Biogenesis Disorder 2 (PEX5) OMIM
   Peroxisome Biogenesis Disorder 3 (PEX12) OMIM
   Peroxisome Biogenesis Disorder 4 (PEX6) OMIM
   Peroxisome Biogenesis Disorder 5 (PEX2) OMIM
   Peroxisome Biogenesis Disorder 6 (PEX10) OMIM
   Peroxisome Biogenesis Disorder 7 (PEX26) OMIM
   Peroxisome Biogenesis Disorder 8 (PEX16) OMIM
   PEX7 Related Disorders (PEX7) OMIM
   PGM3 Related Disorders (PGM3) OMIM
   Phenylalanine Determination - Plasma OMIM GeneReview
   Phenylalanine Hydroxylase Deficiency (PAH) OMIM GeneReview
   Phenylbutyrate Metabolite Analysis
   PHEO and PGL Syndrome Panel (SDHB, SDHC, & SDHD) OMIM GeneReview
   Pheochromocytoma (MAX) OMIM
   Phosphoenolpyruvate carboxykinase-1, cytosolic, deficiency (PCK1) OMIM
   PHOX2B Related Disorders OMIM
   PIK3CA Mutation Analysis - Germline OMIM
   PITX2 Related Disorders OMIM
   PITX3 Related Disorders OMIM
   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
   Polycystic Kidney and Hepatic Disease 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 Hyperoxaluria Type 1 OMIM
   Primary Hyperoxaluria Type II OMIM
   Primary Open Angle Glaucoma (2 gene panel by NGS)
   Primary Open Angle Glaucoma 1A OMIM
   PRKAR1A Related Disorders OMIM
   Proband Whole Exome Sequencing
   Proband Whole Exome Sequencing Plus CMA
   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
   PTCH1 Related Disorders OMIM
   PTEN - Related Disorders OMIM
   PTPN11 - Related Disorders OMIM
   Purine Panel - Urine
   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