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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.



   HADH Related Disorders (HADH) OMIM
   HADHA - Related Disorders OMIM
   HADHB - Related Disorders OMIM
   HARS2 Related disorders OMIM
   Hemochromatosis Panel
   Hemochromatosis Type 1 OMIM
   Hemochromatosis Type 2 A OMIM
   Hemochromatosis Type 2 B OMIM
   Hemochromatosis Type 3 OMIM
   Hemochromatosis Type 4 OMIM
   Hereditary Brain/CNS/PNS Cancer Panel (17 gene panel by NGS)
   Hereditary Breast/Ovarian/Endometrial Cancer Panel (23 gene panel by NGS)
   Hereditary Colorectal/Gastrointestinal Cancer Panel (22 gene panel by NGS)
   Hereditary Endocrine Cancer Panel (15 gene panel by NGS)
   Hereditary Fructose Intolerance (ALDOB) OMIM
   Hereditary Hearing Loss and Deafness - GJB2 Related OMIM GeneReview
   Hereditary Hearing Loss and Deafness - GJB6 Related OMIM GeneReview
   Hereditary Hemorrhagic Telangiectasia Type 1 (ENG) OMIM
   Hereditary Leukemia/Lymphoma Panel (13 gene panel by NGS)
   Hereditary Melanoma Panel (4 gene panel by NGS)
   Hereditary Neuralgic Amyotrophy (HNA) (SEPT9) OMIM
   Hereditary Pancreatic Cancer Panel (16 gene panel by NGS)
   Hereditary Paraganglioma/Pheochromocytoma Panel (9 gene panel by NGS)
   Hereditary Prostate Cancer Panel (5 gene panel by NGS)
   Hereditary Renal Cancer Panel (12 gene panel by NGS)
   Hermansky-Pudlak Syndrome 1 OMIM
   Hermansky-Pudlak Syndrome 3 OMIM
   Hermansky-Pudlak Syndrome 4 OMIM
   Hermansky-Pudlak Syndrome 5 OMIM
   Hermansky-Pudlak Syndrome 6 OMIM
   Hermansky-Pudlak Syndrome 7 OMIM
   Hermansky-Pudlak Syndrome 8 OMIM
   Hexosaminidase A & B Enzyme Analysis OMIM
   Hexosaminidase A Deficiency OMIM GeneReview
   HFE - Associated Hereditary Hemochromatosis OMIM GeneReview
   HHH Syndrome (SLC25A15) OMIM
   High Bone Mass Panel by NGS
   High Risk Hereditary Breast Cancer Panel (7 gene panel by NGS)
   High Risk Hereditary Colorectal Cancer Panel (12 gene panel by NGS)
   HMG-CoA Lyase Deficiency (HMGCL) OMIM
   HMG-CoA synthase-2 deficiency (HMGCS2) OMIM
   HNPCC - EPCAM Related OMIM GeneReview
   HNPCC - MLH1 Related OMIM GeneReview
   HNPCC - MSH2 Related OMIM GeneReview
   HNPCC - MSH6 Related OMIM GeneReview
   HNPCC - PMS2 Related OMIM GeneReview
   HNPCC MSI & IHC Screening OMIM GeneReview
   HNRNPA1 Related Disorders OMIM
   Holocarboxylase Synthetase Deficiency (HLCS , HCS) OMIM
   Homocysteine Determination - Plasma OMIM GeneReview
   Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (CBS) OMIM
   HPD Related Disorders OMIM
   HSD17B4 Related Disorders (HSD17B4) OMIM
   Huntington Disease OMIM GeneReview
   Hyperinsulinism (8 gene panel by NGS) GeneReview
   Hyperinsulinism-Hyperammonemia Syndrome (GLUD1) OMIM
   Hypermethioninemia (GNMT) OMIM
   Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency (AHCY) OMIM
   Hyperprolinemia Type II OMIM
   Hypoglycemia (87 gene panel by NGS)
   Hypophosphatemic Nephrolithiasis/Osteoporosis, 1 (SLC34A1) OMIM