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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.



   LAMA3 Related Disorders OMIM
   LAMB3 Related Disorders OMIM
   LAMC2 Related Disorders OMIM
   LCA5-Related Leber Congenital Amaurosis OMIM
   LCAD Deficiency (ACADL) OMIM
   Leber Congenital Amaurosis Panel (19 gene panel by NGS)
   Leber Congenital Amaurosis, Calcium Binding Protein 4 Deficiency (CABP4) OMIM GeneReview
   Leber Congenital Amaurosis, IQ Motif Containing B1 Deficiency (IQCB1) OMIM GeneReview
   Leigh Disease (91 gene panel by NGS) GeneReview
   Leigh Syndrome - LRPPRC OMIM
   Lesch-Nyhan Syndrome OMIM GeneReview
   Leukoencephalopathy (DARS2) OMIM GeneReview
   Leukoencephalopathy with dystonia and motor neuropathy (SCP2) OMIM
   Li-Fraumeni Syndrome OMIM GeneReview
   Li-Fraumeni syndrome with brain tumours
   Liver Failure, Acute Infantile (TRMU) OMIM
   LMBRD1 (cblF)-Related Disorders OMIM GeneReview
   Low Bone Mass Panel by NGS (23 gene panel by NGS)
   Lowe Syndrome OMIM GeneReview
   LRAT-Related Retinitis Pigmentosa OMIM
   LRP5 Related Disorders OMIM
   Lysinuric Protein Intolerance OMIM
   Lysosomal Acid Lipase Deficiency OMIM