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True Health Diagnostics

  • True Health Diagnostics, THD
  • Richmond, Virginia, United States 23219
  • Phone: 804-343-2718 (U.S.A)
    Email: wxu@truehealthdiag.com

GTR Lab ID: 506273, Last updated:2018-07-16

Personnel

Conditions and tests

  • Acute neuronopathic Gaucher's disease4 tests
  • Adrenoleukodystrophy1 test
  • Alkaptonuria1 test
  • alpha Thalassemia3 tests
  • Aspartylglucosaminuria1 test
  • Ataxia with vitamin E deficiency1 test
  • Ataxia-telangiectasia syndrome1 test
  • Autosomal recessive polycystic kidney disease1 test
  • Bardet-Biedl syndrome1 test
  • Becker muscular dystrophy2 tests
  • beta Thalassemia3 tests
  • Biotinidase deficiency1 test
  • Bloom syndrome4 tests
  • Breast cancer, early-onset1 test
  • Breast cancer, susceptibility to1 test
  • Breast-ovarian cancer, familial 11 test
  • Breast-ovarian cancer, familial 21 test
  • Breast-ovarian cancer, familial 31 test
  • Breast-ovarian cancer, familial 41 test
  • Carbohydrate-deficient glycoprotein syndrome type I1 test
  • Carcinoma of colon1 test
  • Carcinoma of pancreas1 test
  • Ceroid lipofuscinosis neuronal 11 test
  • Ceroid lipofuscinosis neuronal 21 test
  • Ceroid lipofuscinosis neuronal 51 test
  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
  • Clopidogrel response1 test
  • Colorectal cancer 101 test
  • Colorectal cancer, susceptibility to, 121 test
  • Cowden syndrome 11 test
  • Cutaneous malignant melanoma 21 test
  • Cutaneous malignant melanoma 31 test
  • Cystic fibrosis5 tests
  • Deafness, autosomal recessive 1A1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Dihydropyrimidine dehydrogenase deficiency1 test
  • Duchenne muscular dystrophy2 tests
  • Endometrial carcinoma1 test
  • Familial adenomatous polyposis 11 test
  • Familial cancer of breast1 test
  • Familial colorectal cancer1 test
  • Familial dysautonomia4 tests
  • Familial Mediterranean fever1 test
  • Familial pancreatic carcinoma1 test
  • Familial type 3 hyperlipoproteinemia1 test
  • Fanconi anemia, complementation group C4 tests
  • Fragile X syndrome1 test
  • Fukuyama congenital muscular dystrophy2 tests
  • Gaucher disease, perinatal lethal4 tests
  • Glutaric aciduria, type 11 test
  • Glycogen storage disease type 1A3 tests
  • Glycogen storage disease type III1 test
  • Glycogen storage disease, type II1 test
  • Hb SS disease3 tests
  • Hereditary breast and ovarian cancer syndrome1 test
  • Hereditary diffuse gastric cancer1 test
  • Hereditary factor XI deficiency disease1 test
  • Hereditary fructosuria1 test
  • Hereditary mixed polyposis syndrome 21 test
  • Hereditary nonpolyposis colorectal cancer type 41 test
  • Hereditary nonpolyposis colorectal cancer type 51 test
  • Hereditary nonpolyposis colorectal cancer type 81 test
  • Hereditary ovarian carcinoma1 test
  • Homocystinuria due to CBS deficiency1 test
  • Hyperhomocysteinemia1 test
  • Hypophosphatasia1 test
  • I cell disease1 test
  • Infantile GM1 gangliosidosis1 test
  • Islet cell hyperplasia1 test
  • Joubert syndrome 23 tests
  • Juvenile retinoschisis1 test
  • Leigh syndrome, French Canadian type1 test
  • Li-Fraumeni syndrome 11 test
  • Li-Fraumeni syndrome 21 test
  • Lynch syndrome I1 test
  • Lynch syndrome II1 test
  • Malignant tumor of prostate1 test
  • Maple syrup urine disease3 tests
  • Maple syrup urine disease, type 33 tests
  • Meckel syndrome type 11 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Melanoma-pancreatic cancer syndrome1 test
  • Metachromatic leukodystrophy1 test
  • Metaphyseal chondrodysplasia, McKusick type1 test
  • Mucolipidosis type IV4 tests
  • Muir-Torré syndrome1 test
  • Muscle eye brain disease1 test
  • MYH-associated polyposis1 test
  • Nemaline myopathy 23 tests
  • Nemaline myopathy 51 test
  • Neoplasm of the breast1 test
  • Nephronophthisis 11 test
  • Nephropathic cystinosis1 test
  • Niemann-Pick disease type C11 test
  • Niemann-Pick disease, type A4 tests
  • Osteochondrodysplasia1 test
  • Osteosarcoma1 test
  • Pancreatic cancer 21 test
  • Pancreatic cancer 31 test
  • Pendred syndrome1 test
  • Persistent hyperinsulinemic hypoglycemia of infancy3 tests
  • Peutz-Jeghers syndrome1 test
  • Phenylketonuria1 test
  • Pilomatrixoma1 test
  • Pituitary hormone deficiency, combined 21 test
  • Polyglandular autoimmune syndrome, type 11 test
  • Renal carnitine transport defect1 test
  • Salla disease1 test
  • Sandhoff disease4 tests
  • Sjögren-Larsson syndrome1 test
  • Smith-Lemli-Opitz syndrome1 test
  • Spinal muscular atrophy type 45 tests
  • Spongy degeneration of central nervous system4 tests
  • Tay-Sachs disease4 tests
  • Thrombophilia due to factor V Leiden1 test
  • Turcot syndrome1 test
  • Tyrosinemia type I1 test
  • Usher syndrome, type 11 test
  • Usher syndrome, type 1C1 test
  • Usher syndrome, type 1D3 tests
  • Usher syndrome, type 3A3 tests
  • Venous thrombosis1 test
  • Very long chain acyl-CoA dehydrogenase deficiency1 test
  • Vitamin D-dependent rickets, type 11 test
  • Warfarin response1 test
  • Wilson disease1 test
  • Wiskott-Aldrich syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously, comments

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 49D1100708, Expiration date: 2020-02-18
  • CAP, Number: 7224971, Expiration date: 2019-11-11

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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