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Genetic Labs

Houston, Texas

Genetic Laboratory
Medical Genetics Laboratories
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Medical Genetics Test Services

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  HADH Related Disorders (HADH) OMIM
  HADHA - Related Disorders OMIM
  HADHB - Related Disorders OMIM
  HARS2 Related disorders OMIM
  Hereditary Brain/CNS/PNS Cancer Panel
  Hereditary Breast/Ovarian Cancer Panel
  Hereditary Breast/Ovarian Cancer Panel (without BRCA1/2)
  Hereditary Endocrine Cancer Panel
  Hereditary Fructose Intolerance (ALDOB) OMIM
  Hereditary GI/Colorectal Cancer Panel
  Hereditary Hearing Loss and Deafness - GJB2 Related OMIM GeneReview
  Hereditary Hearing Loss and Deafness - GJB6 Related OMIM GeneReview
  Hereditary High Risk Breast Cancer Panel
  Hereditary High Risk Colorectal Cancer Panel
  Hereditary Neuralgic Amyotrophy (HNA) (SEPT9) OMIM
  Hereditary Pheochromocytoma-Paraganglioma Cancer Panel
  Hereditary Renal Cancer Panel
  Hermansky-Pudlak Syndrome 1 OMIM
  Hermansky-Pudlak Syndrome 2 (AP3B1) 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
  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 Comprehensive Panel (MLH1, MSH2, & MSH6) OMIM GeneReview
  HNPCC MSI & IHC Screening OMIM GeneReview
  HNPCC PLUS Comprehensive Panel (MLH1, MSH2, MSH6, PMS2, EPCAM)
  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
  Hypermethioninemia (GNMT) OMIM
  Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency (AHCY) OMIM
  Hyperprolinemia Type II OMIM
  Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis (SARS2) OMIM
  Hypophosphatemic Nephrolithiasis/Osteoporosis, 1 (SLC34A1) OMIM