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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.



   ABCA4 - Related Disorders OMIM GeneReview
   Acetyl-CoA Carboxylase Deficiency (ACACA) OMIM
   Achondroplasia OMIM GeneReview
   Acute Lymphoblastic Leukaemia (PAX5) OMIM
   Acute Myeloid Leukemia (CEBPA) OMIM
   Acute Recurrent Myoglobinuria - LPIN1 Related OMIM
   Acylcarnitine Analysis - Plasma OMIM
   Acyl-CoA Dehydrogenase 9 Deficiency (ACAD9) OMIM
   Acyl-CoA Dehydrogenase, Short/Branched Chain Deficiency (ACADSB) OMIM
   Additional Affected Sibling for Trio
   Adenine Phosphoribosyltransferase Deficiency (APRT) OMIM
   Adenosine Deaminase Deficiency OMIM GeneReview
   Adenosine Deaminase Deficiency (ADA) OMIM
   Adenylosuccinase Deficiency (ADSL) OMIM
   Adrenoleukodystrophy (ABCD1) OMIM GeneReview
   Adult Screening Exome Sequencing
   Agenesis of the Corpus Callosum with Peripheral Neuropathy OMIM
   AIFM1 Related Disorders OMIM
   Alagille Syndrome (JAG1) OMIM GeneReview
   Albinism (13 gene panel by NGS)
   ALK Gene Rearrangement by FISH Analysis OMIM
   Alpha-Mannosidosis Types I and II OMIM
   ALPL Related Disorders OMIM
   AMACR Related Disorders (AMACR) OMIM
   Amino Acid Analysis - Cerebrospinal Fluid
   Amino Acid Analysis - Plasma
   Amino Acid Analysis - Urine
   Androgen Insensitivity Syndrome OMIM GeneReview
   Angelman Syndrome OMIM GeneReview
   APC - Associated Polyposis Conditions OMIM GeneReview
   Arginase Deficiency OMIM GeneReview
   Arginine: Glycine Amidinotransferase (GATM) Deficiency (AGAT) OMIM GeneReview
   Argininosuccinate Lyase Deficiency OMIM GeneReview
   ARL6 Related Disorders OMIM
   ARX - Related Disorders OMIM
   Arylsulfatase A Deficiency [Metachromatic Leukodystrophy] OMIM GeneReview
   Aspartylglycosaminuria (AGA) OMIM
   Ataxia with Isolated Vitamin E Deficiency OMIM
   Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (APTX) OMIM
   Ataxia-Telangiectasia-like Disorder (MRE11A) OMIM
   ATM Related Disorders OMIM
   ATP5A1 Related disorders OMIM
   ATP6V0A2 Related Disorders OMIM
   Autism Panel - Biochemistry 3-Plex
   Autism Panel - Biochemistry 5- Plex
   Autism Panel - Biochemistry 8-Plex
   Autoimmune Polyendocrinopathy 1 OMIM