Otogenetics

Personnel

Director: Larry Hung, MD, ABPath, Lab Director
Phone: http://www.otogenetics.com/
Email: lhung@otogenetics.com
Angela Alexander, PhD, MS, Staff

Conditions and tests

158 conditions/phenotypes with 3 tests
Enter text to narrow down the list

Alagille syndrome due to a JAG1 point mutation1 test
Aminoglycoside-induced deafness1 test
Anophthalmia/microphthalmia-esophageal atresia syndrome1 test
Atrophia bulborum hereditaria1 test
Autoimmune lymphoproliferative syndrome type 11 test
Autosomal dominant deafness - onychodystrophy syndrome1 test
Autosomal dominant nonsyndromic hearing loss 11 test
Autosomal dominant nonsyndromic hearing loss 101 test
Autosomal dominant nonsyndromic hearing loss 111 test
Autosomal dominant nonsyndromic hearing loss 121 test
Autosomal dominant nonsyndromic hearing loss 131 test
Autosomal dominant nonsyndromic hearing loss 151 test
Autosomal dominant nonsyndromic hearing loss 171 test
Autosomal dominant nonsyndromic hearing loss 201 test
Autosomal dominant nonsyndromic hearing loss 221 test
Autosomal dominant nonsyndromic hearing loss 231 test
Autosomal dominant nonsyndromic hearing loss 251 test
Autosomal dominant nonsyndromic hearing loss 281 test
Autosomal dominant nonsyndromic hearing loss 2A1 test
Autosomal dominant nonsyndromic hearing loss 2B1 test
Autosomal dominant nonsyndromic hearing loss 361 test
Autosomal dominant nonsyndromic hearing loss 401 test
Autosomal dominant nonsyndromic hearing loss 411 test
Autosomal dominant nonsyndromic hearing loss 441 test
Autosomal dominant nonsyndromic hearing loss 481 test
Autosomal dominant nonsyndromic hearing loss 4A1 test
Autosomal dominant nonsyndromic hearing loss 4B1 test
Autosomal dominant nonsyndromic hearing loss 51 test
Autosomal dominant nonsyndromic hearing loss 511 test
Autosomal dominant nonsyndromic hearing loss 61 test
Autosomal dominant nonsyndromic hearing loss 91 test
Autosomal recessive nonsyndromic hearing loss 151 test
Autosomal recessive nonsyndromic hearing loss 161 test
Autosomal recessive nonsyndromic hearing loss 221 test
Autosomal recessive nonsyndromic hearing loss 241 test
Autosomal recessive nonsyndromic hearing loss 251 test
Autosomal recessive nonsyndromic hearing loss 281 test
Autosomal recessive nonsyndromic hearing loss 291 test
Autosomal recessive nonsyndromic hearing loss 31 test
Autosomal recessive nonsyndromic hearing loss 301 test
Autosomal recessive nonsyndromic hearing loss 311 test
Autosomal recessive nonsyndromic hearing loss 351 test
Autosomal recessive nonsyndromic hearing loss 361 test
Autosomal recessive nonsyndromic hearing loss 391 test
Autosomal recessive nonsyndromic hearing loss 41 test
Autosomal recessive nonsyndromic hearing loss 421 test
Autosomal recessive nonsyndromic hearing loss 491 test
Autosomal recessive nonsyndromic hearing loss 591 test
Autosomal recessive nonsyndromic hearing loss 61 test
Autosomal recessive nonsyndromic hearing loss 611 test
Autosomal recessive nonsyndromic hearing loss 631 test
Autosomal recessive nonsyndromic hearing loss 671 test
Autosomal recessive nonsyndromic hearing loss 741 test
Autosomal recessive nonsyndromic hearing loss 771 test
Autosomal recessive nonsyndromic hearing loss 791 test
Autosomal recessive nonsyndromic hearing loss 84A1 test
Autosomal recessive nonsyndromic hearing loss 91 test
Autosomal recessive nonsyndromic hearing loss 911 test
Baraitser-Winter syndrome 11 test
Baraitser-winter syndrome 21 test
Bartter disease type 4A1 test
Bosch-Boonstra-Schaaf optic atrophy syndrome1 test
Branchiootorenal syndrome 21 test
Breast and colorectal cancer1 test
Breast and colorectal cancer, susceptibility to1 test
Breast cancer, early-onset1 test
Breast cancer, familial male1 test
Breast cancer, susceptibility to1 test
Breast neoplasm1 test
Breast-ovarian cancer, familial, susceptibility to, 11 test
Breast-ovarian cancer, familial, susceptibility to, 21 test
Breast-ovarian cancer, familial, susceptibility to, 31 test
Breast-ovarian cancer, familial, susceptibility to, 41 test
Carcinoma of colon1 test
Cerebrooculofacioskeletal syndrome 21 test
Charcot-Marie-Tooth disease type 1E1 test
Charcot-Marie-Tooth disease X-linked dominant 11 test
Charcot-Marie-Tooth disease, type IA1 test
Chudley-McCullough syndrome1 test
Colorectal cancer1 test
Corneal dystrophy-perceptive deafness syndrome1 test
Costello syndrome1 test
Cowden syndrome1 test
Craniofacial-deafness-hand syndrome1 test
Craniometaphyseal dysplasia, autosomal recessive1 test
Deafness dystonia syndrome1 test
Deafness with labyrinthine aplasia, microtia, and microdontia1 test
Deafness, autosomal dominant 39, with dentinogenesis imperfecta 11 test
Deafness-infertility syndrome1 test
Developmental malformations-deafness-dystonia syndrome1 test
DFNA 3 Nonsyndromic Hearing Loss and Deafness1 test
Exudative vitreoretinopathy 2, X-linked1 test
Familial adenomatous polyposis 11 test
Familial cancer of breast1 test
Familial colorectal cancer1 test
Familial medullary thyroid carcinoma1 test
Familial pancreatic carcinoma1 test
Familial prostate cancer1 test
Fanconi anemia1 test
GJB4-Related Erythrokeratodermia Variabilis1 test
Hereditary breast ovarian cancer syndrome1 test
Hereditary cancer-predisposing syndrome1 test
Hereditary diffuse gastric adenocarcinoma1 test
Hereditary disease1 test
Hereditary hearing loss and deafness1 test
Hereditary nonpolyposis colon cancer1 test
Hirschsprung disease, cardiac defects, and autonomic dysfunction1 test
Hirschsprung disease, susceptibility to, 21 test
Histidinemia1 test
Hypoparathyroidism, deafness, renal disease syndrome1 test
Jervell and Lange-Nielsen syndrome 11 test
Jervell and Lange-Nielsen syndrome 21 test
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
Juvenile polyposis syndrome1 test
Li-Fraumeni syndrome1 test
Long QT syndrome 11 test
Long QT syndrome 51 test
Malignant tumor of urinary bladder1 test
Mandibulofacial dysostosis with alopecia1 test
Melanoma-pancreatic cancer syndrome1 test
MERRF syndrome1 test
Mitochondrial non-syndromic sensorineural hearing loss1 test
Muenke syndrome1 test
Multiple endocrine neoplasia, type 11 test
Multiple endocrine neoplasia, type 21 test
Netherton syndrome1 test
Nijmegen breakage syndrome-like disorder1 test
Non-acquired combined pituitary hormone deficiency with spine abnormalities1 test
Nonsyndromic Deafness1 test
Ocular albinism with congenital sensorineural hearing loss1 test
Pendred syndrome1 test
Peutz-Jeghers syndrome1 test
Pili torti-deafness syndrome1 test
PTEN hamartoma tumor syndrome1 test
Renal tubular acidosis with progressive nerve deafness1 test
Sensorineural hearing loss disorder1 test
Short QT syndrome type 21 test
Spermatogenic failure 71 test
Stickler syndrome1 test
Urinary bladder carcinoma1 test
Usher syndrome type 12 tests
Usher syndrome type 1C2 tests
Usher syndrome type 1D2 tests
Usher syndrome type 1F2 tests
Usher syndrome type 1G2 tests
Usher syndrome type 2A2 tests
Usher syndrome type 2C2 tests
Usher syndrome type 2D2 tests
Usher syndrome type 32 tests
Usher syndrome, type IIC, GPR98/PDZD7 digenic2 tests
Von Hippel-Lindau syndrome1 test
Waardenburg syndrome type 11 test
Waardenburg syndrome type 2D1 test
Waardenburg syndrome type 31 test
X-linked deafness1 test
X-linked mixed hearing loss with perilymphatic gusher1 test
Xeroderma pigmentosum group B1 test
Zimmermann-Laband syndrome 21 test

List of services

Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses

Certifications

CLIAHelpCertification number assigned by the Clinical Laboratory Improvement Amendments (CLIA) program to the laboratory director. Minimal field for US labs offering clinical tests. Optional field for international labs or US labs performing research tests. If pending renewal or record has not been updated, the expiration date may be in the past., Number: 11D2066426, Expiration date: 2023-09-02
CAP, Number: 8702957, Expiration date: 2025-05-17

Licenses

CA - California Department of Public Health CDPH, Number: CDS 00800657, Expiration date: 2023-12-09
GA - Georgia Department of Community Health DCH, Number: 067-071, Effective date: 2019-02-28 Non-expiring
PA - Pennsylvania Department of Health PADOH, Number: 37090, Expiration date: 2024-08-15

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.