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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Miraca 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
  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 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
  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
  HNF1A Related Disorders OMIM
  HNF1B Related Disorders 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)
  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
  Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis (SARS2) OMIM
  Hypophosphatemic Nephrolithiasis/Osteoporosis, 1 (SLC34A1) OMIM