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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.



   SAG-Related Retinitis Pigmentosa OMIM
   SCAD Deficiency (ACADS) OMIM GeneReview
   Schmid Metaphyseal Chondrodysplasia OMIM
   SCID Newborn Screening Follow-up Panel
   SCO1 - Related Disorders OMIM
   SCO2 - Related Disorders (SCO2 or SCO1L) OMIM
   SDHA - Related Disorders OMIM
   SDHB - Related Disorders OMIM GeneReview
   SDHC - Related Disorders OMIM GeneReview
   SDHD - Related Disorders OMIM GeneReview
   Segawa Syndrome Recessive OMIM
   Sequential Trio Whole Exome Sequencing
   SERPINA1 Related Disorders (SERPINA1) OMIM
   Severe Combined Immunodeficiency, Athabascan Type OMIM
   Severe Combined Immunodeficiency, Autosomal Recessive, T- Negative/B-Positive Type OMIM
   Severe Combined Immunodeficiency, B Cell-Negative OMIM
   Shwachman-Bodian-Diamond Syndrome OMIM
   Sickle Cell Disease OMIM GeneReview
   SIRT1 Related Disorders OMIM
   Sjogren-Larsson Syndrome OMIM
   SLC16A1 Related Disorders OMIM
   SLC17A5 Related Disorders OMIM
   SLC25A4 (ANT1) - Related Disorders OMIM
   SLC26A2 Related Disorders OMIM
   SLC26A4 Related Disorders OMIM
   SMAD4 Related Disorders OMIM
   Smith-Lemli-Opitz Syndrome OMIM GeneReview
   Smith-Magenis Syndrome OMIM GeneReview
   SMPD1 Related Disorders OMIM
   Spastic Ataxia Charlevoix-Saguenay Type OMIM
   Spastic Paraplegia 7, Autosomal Recessive (SPG7) OMIM
   Spinal Muscular Atrophy Diagnostic Test OMIM GeneReview
   Spinocerebellar Ataxia Type 14 (PRKCG) OMIM
   Spondylocheirodysplasia, Ehlers-Danlos Syndrome (SLC39A13) OMIM
   SRD5A3 Related Disorders OMIM
   SRY Molecular Analysis OMIM GeneReview
   STK11 Related Disorders OMIM
   Succinic Semialdehyde Dehydrogenase Deficiency (ALDH5A1) OMIM
   Succinyladenosine - CSF
   SUCLA2 - Related Disorders OMIM GeneReview
   SUCLG1 - Related Disorders OMIM
   Sulfocysteine Determination - Urine OMIM
   SURF1 - Related Disorders OMIM