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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.



   C10orf2 (TWINKLE) - Related Disorders OMIM
   C2orf71-Related Retinitis Pigmentosa OMIM
   CA4-Related Retinitis Pigmentosa OMIM
   CALR (Calreticulin) Exon 9 Mutation Analysis by PCR
   Camurati-Engelmann Disease (TGFB1) OMIM
   Carbamoyl Phosphate Synthetase Deficiency (CPS1) OMIM GeneReview
   Carnitine Acylcarnitine Translocase (CACT) Deficiency (SLC25A20 ) OMIM
   Carnitine Deficiency, Systemic (SLC22A5 (OCTN2)) OMIM
   Carnitine Determination - Plasma OMIM
   Carnitine Palmitoyltransferase IA Deficiency (CPT1A ) OMIM GeneReview
   Carnitine Palmitoyltransferase II Deficiency (CPT2) OMIM GeneReview
   CDH23 - Related Disorders OMIM
   CDKL5 - Related Disorders OMIM
   CEBPA Mutation Detection
   CEP290-Related Retinitis Pigmentosa OMIM
   CFTR - 5T Variant Analysis OMIM GeneReview
   CFTR Sequence Analysis OMIM GeneReview
   CHD7 - Related Disorders OMIM
   Cholestasis Panel by NGS (7 gene panel by NGS)
   CHRNA7 - Related Disorders OMIM
   Chromosomal Microarray Analysis
   Chromosomal Microarray Analysis - HR
   Chromosomal Microarray Analysis - HR + SNP Screen (Comprehensive)
   Chromosome Analysis - Blood
   Chromosome Analysis - Prenatal - Amniotic Fluid
   Chromosome Analysis - Prenatal - Amniotic Fluid with ACHE
   Chromosome Analysis - Prenatal - Amniotic Fluid with AFP
   Chromosome Analysis - Prenatal - CVS
   Chromosome Analysis - Tissue
   Citrin Deficiency (SLC25A13) OMIM GeneReview
   ClariFindTM FISH Panel
   Cleidocranial Dysplasia OMIM GeneReview
   CMA-Expanded and Limited Karyotype - Prenatal - Amniotic Fluid
   CMA-Expanded and Limited Karyotype - Prenatal - CVS
   CMA-Targeted and Limited Karyotype - Prenatal - Amniotic Fluid
   CMA-Targeted and Limited Karyotype - Prenatal - CVS
   CNGB1-Related Retinitis Pigmentosa OMIM
   Cobalamin Metabolism Panel (20 gene panel by NGS)
   Coenzyme Q10 Deficiency - CABC1 (ADCK3) Related OMIM
   Coenzyme Q10 Deficiency - COQ2 Related (COQ2, CL640, FLJ26072) OMIM
   Coenzyme Q10 Deficiency - PDSS2 Related (PDSS2, bA59I9.3) OMIM
   COL1A1/2 Related Disorders (2 gene panel by NGS)
   COL2A1 - Related Disorders OMIM GeneReview
   Combined Malonic & Methylmalonic Aciduria (ACSF3) OMIM
   Combined Oxidative Phosphorylation Deficiency - TSFM Related (EF-TS, EF-Tsmt) OMIM
   Combined Oxidative Phosphorylation Deficiency 1 (GFM1) OMIM
   Combined Oxidative Phosphorylation Deficiency 5 (MRPS22) OMIM
   Combined Oxidative Phosphorylation Deficiency 7 (C12orf65) OMIM
   Combined Oxidative Phosphorylation Deficiency 8 (AARS2) OMIM
   Common Hereditary Cancer Panel (43-gene panel by NGS)
   Comprehensive Autism Panel - Female Specific
   Comprehensive Autism Panel - Male Specific
   Comprehensive Hereditary Cancer Panel (94-gene panel by NGS)
   Cone-rod Dystrophy 15 (CDHR1) OMIM
   Congenital Disorder of Glycosylation, Type Iv (NGLY1) OMIM
   Congenital Disorders of Glycosylation - CDG Panel (36 gene panel by NGS) GeneReview
   Congenital Disorders of Glycosylation MPI Related OMIM GeneReview
   Congenital Disorders of Glycosylation PMM2 Related OMIM GeneReview
   Congenital Disorders of Glycosylation Type Ik OMIM GeneReview
   Congenital Disorders of Glycosylation Type Im (DOLK) OMIM GeneReview
   Congenital Hypothyroidism, IYD-Related OMIM
   CoQ10 Deficiency (5 gene panel by NGS) OMIM
   Coronary Heart Disease Risk Factor (9p21 rs10757278)
   Costello Syndrome - HRAS Related OMIM GeneReview
   COX10 - Related Disorders OMIM
   COX15 - Related Disorders OMIM
   CPT1B - Related Disorders OMIM
   CRB1-Related Retinitis Pigmentosa OMIM
   Creatine and Guanidinoacetate Determination - Plasma OMIM GeneReview
   Creatine and Guanidinoacetate Determination - Urine OMIM GeneReview
   Creatine Panel
   Creatine Transporter Deficiency - SLC6A8 Related OMIM GeneReview
   Critical Trio Whole Exome Sequencing
   CRX-Related Retinitis Pigmentosa OMIM
   Custom Family Sequence Analysis
   Custom Proband Sequence Analysis
   Custom Sequence Analysis - Prenatal
   Custom Sequence Analysis - Proband