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GTR Home > Laboratories > GeneID Lab - Advanced Molecular Diagnostics

GeneID Lab - Advanced Molecular Diagnostics

GTR Lab ID: 506582, Last updated:2023-04-04

Personnel

  • Director: Daniel Cohen, MD, Lab Director

Conditions and tests

  • Acute lymphoid leukemia1 test
  • Adult-onset proximal spinal muscular atrophy, autosomal dominant1 test
  • alpha Thalassemia1 test
  • Amyotrophic lateral sclerosis type 81 test
  • Aneurysm-osteoarthritis syndrome1 test
  • Aortic aneurysm, familial thoracic 41 test
  • Aortic aneurysm, familial thoracic 61 test
  • Aortic aneurysm, familial thoracic 71 test
  • Aplastic anemia2 tests
  • Arterial tortuosity syndrome1 test
  • Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures1 test
  • Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome1 test
  • Autosomal dominant nonsyndromic hearing loss 131 test
  • Autosomal dominant nonsyndromic hearing loss 2A1 test
  • Autosomal dominant nonsyndromic hearing loss 2B1 test
  • Autosomal dominant nonsyndromic hearing loss 3A1 test
  • Autosomal dominant nonsyndromic hearing loss 3B1 test
  • Autosomal recessive nonsyndromic hearing loss 1A1 test
  • Autosomal recessive pseudohypoaldosteronism type 11 test
  • Baller-Gerold syndrome1 test
  • Bannayan-Riley-Ruvalcaba syndrome2 tests
  • BAP1-related tumor predisposition syndrome2 tests
  • Basal cell carcinoma, somatic1 test
  • beta Thalassemia1 test
  • Bloom syndrome1 test
  • Breast and colorectal cancer, susceptibility to3 tests
  • Breast lobular carcinoma2 tests
  • Breast-ovarian cancer, familial, susceptibility to, 14 tests
  • Breast-ovarian cancer, familial, susceptibility to, 23 tests
  • Breast-ovarian cancer, familial, susceptibility to, 32 tests
  • Breast-ovarian cancer, familial, susceptibility to, 42 tests
  • Bronchiectasis with or without elevated sweat chloride 11 test
  • Bronchiectasis with or without elevated sweat chloride 21 test
  • Bronchiectasis with or without elevated sweat chloride 31 test
  • Canavan Disease, Familial Form1 test
  • Carcinoma of colon1 test
  • Carcinoma of pancreas1 test
  • Colorectal cancer, hereditary nonpolyposis, type 24 tests
  • Colorectal cancer, susceptibility to2 tests
  • Colorectal cancer, susceptibility to, 102 tests
  • Colorectal cancer, susceptibility to, 122 tests
  • Cowden syndrome 12 tests
  • Cystic fibrosis1 test
  • Decreased activity of the pyruvate dehydrogenase complex1 test
  • Ehlers-Danlos syndrome, type 41 test
  • Endometrial carcinoma1 test
  • Familial adenomatous polyposis 12 tests
  • Familial adenomatous polyposis 22 tests
  • Familial cancer of breast2 tests
  • Familial colorectal cancer3 tests
  • Familial dysautonomia1 test
  • Familial melanoma2 tests
  • Familial pancreatic carcinoma1 test
  • Familial thoracic aortic aneurysm and aortic dissection1 test
  • Fanconi anemia complementation group A1 test
  • Fanconi anemia complementation group C1 test
  • Fanconi anemia complementation group F1 test
  • Fanconi anemia complementation group G1 test
  • Fanconi anemia complementation group O2 tests
  • Fragile X syndrome1 test
  • Galactosemia1 test
  • Gaucher disease1 test
  • Generalized juvenile polyposis/juvenile polyposis coli2 tests
  • Glycogen storage disease, type II1 test
  • Glycogen storage disease, type IV1 test
  • Gorlin syndrome1 test
  • Hb SS disease1 test
  • Hereditary breast ovarian cancer syndrome4 tests
  • Hereditary cancer-predisposing syndrome4 tests
  • Hereditary diffuse gastric adenocarcinoma2 tests
  • Hereditary nonpolyposis colon cancer1 test
  • Infantile-onset X-linked spinal muscular atrophy1 test
  • Isolated hyperchlorhidrosis1 test
  • Jervell and Lange-Nielsen syndrome 11 test
  • Jervell and Lange-Nielsen syndrome 21 test
  • Juvenile Polyposis1 test
  • Leukemia, acute lymphoblastic, susceptibility to1 test
  • Li-Fraumeni syndrome 13 tests
  • Li-Fraumeni syndrome 23 tests
  • Liddle syndrome 11 test
  • Liddle syndrome 21 test
  • Liddle syndrome 31 test
  • Loeys-Dietz syndrome 11 test
  • Loeys-Dietz syndrome 21 test
  • Long QT syndrome 11 test
  • Long QT syndrome 111 test
  • Long QT syndrome 31 test
  • Long QT syndrome 51 test
  • Long QT syndrome 61 test
  • Lung adenocarcinoma1 test
  • Lymphoma, non-Hodgkin, familial1 test
  • Lynch syndrome2 tests
  • Lynch syndrome 14 tests
  • Lynch syndrome 44 tests
  • Lynch syndrome 54 tests
  • Lynch syndrome 83 tests
  • Malignant melanoma of skin1 test
  • Malignant tumor of breast1 test
  • Malignant tumor of prostate1 test
  • Maple syrup urine disease type 1A1 test
  • Maple syrup urine disease type 1B1 test
  • Maple syrup urine disease type 21 test
  • Marfan syndrome1 test
  • Melanoma, cutaneous malignant, susceptibility to, 22 tests
  • Melanoma, cutaneous malignant, susceptibility to, 31 test
  • Melanoma-pancreatic cancer syndrome2 tests
  • Mucolipidosis type IV1 test
  • Muir-TorrĂ© syndrome2 tests
  • Multiple endocrine neoplasia, type 2a1 test
  • Multiple endocrine neoplasia, type 2b1 test
  • Multiple myeloma1 test
  • Neoplasm2 tests
  • Neoplasm of the large intestine1 test
  • Niemann-Pick disease, type C11 test
  • Niemann-Pick disease, type C21 test
  • Nijmegen breakage syndrome-like disorder1 test
  • Non-Hodgkin lymphoma2 tests
  • Ornithine carbamoyltransferase deficiency1 test
  • Pancreatic cancer, susceptibility to, 21 test
  • Pancreatic cancer, susceptibility to, 32 tests
  • Pancreatic cancer, susceptibility to, 42 tests
  • Papillary renal cell carcinoma type 12 tests
  • Pendred syndrome1 test
  • Peutz-Jeghers syndrome2 tests
  • Phenylketonuria1 test
  • Pheochromocytoma1 test
  • Polyposis syndrome, hereditary mixed, 11 test
  • Prostate cancer susceptibility2 tests
  • Prostate cancer, hereditary, 22 tests
  • Proteus syndrome2 tests
  • Proteus-like syndrome2 tests
  • PTEN hamartoma tumor syndrome2 tests
  • Pyruvate dehydrogenase E3 deficiency1 test
  • Rapadilino syndrome1 test
  • Renal cell carcinoma1 test
  • Rothmund-Thomson syndrome1 test
  • Spinal muscular atrophy1 test
  • Tay-Sachs disease1 test
  • Turcot syndrome4 tests
  • Usher syndrome type 11 test
  • Usher syndrome type 1B1 test
  • Usher syndrome type 1C1 test
  • Usher syndrome type 1D1 test
  • Usher syndrome type 1F1 test
  • Usher syndrome type 2A1 test
  • Usher Syndrome, Type 1A1 test
  • Werdnig-Hoffmann disease1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Carrier testing
  • Whole Exome Sequencing

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 31D2053667, Expiration date: 2024-07-22
  • CAP, Number: 8739211, Expiration date: 2024-03-13

Licenses

  • CA - California Department of Public Health CDPH, Number: CDS00800425, Expiration date: 2023-10-03
  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 1985, Effective date: 2018-07-01 Non-expiring
  • NJ - State of New jersey Department of Health and Senior Service, Number: 00062756, Expiration date: 2023-12-31
  • RI - State of Rhode Island Department of Health RIDOH, Number: LCO01253, Expiration date: 2024-12-30

Participation in external programs

Data exchange Programs

  • Mutation-specific Databases

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