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GTR Home > Laboratories > Molecular Otolaryngology and Renal Research Laboratories

Molecular Otolaryngology and Renal Research Laboratories

GTR Lab ID: 1119, Last updated:2024-01-11

Personnel

  • Director: Richard Smith, MD, ABOto, Lab Director
    Phone: 319-356-3612
    Fax: 319-356-4108
    Email: richard-smith@uiowa.edu
    Contact note: morl@uiowa.edu
  • Amy Weaver, Administrator
    Phone: 319-335-6623
    Fax: 319-335-9890
    Email: amy-weaver@uiowa.edu
    Contact note: morl@uiowa.edu
  • Jori Hendon, BA, Administrator
    Phone: 319-335-6653
    Fax: 319-335-9890
    Email: jori-hendon@uiowa.edu
    Contact note: morl@uiowa.edu

Conditions and tests

  • 3MC syndrome 11 test
  • Alpha mannosidosis type II1 test
  • Alport syndrome1 test
  • Alstrom syndrome1 test
  • Amikacin response1 test
  • Aminoglycoside antibacterials response1 test
  • Aminoglycoside-induced deafness2 tests
  • Anemia, nonspherocytic hemolytic, due to G6PD deficiency2 tests
  • Atrophia bulborum hereditaria1 test
  • Atypical hemolytic-uremic syndrome1 test
  • Atypical hemolytic-uremic syndrome with B factor anomaly1 test
  • Atypical hemolytic-uremic syndrome with C3 anomaly1 test
  • Atypical hemolytic-uremic syndrome with I factor anomaly1 test
  • Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly1 test
  • Atypical hemolytic-uremic syndrome with thrombomodulin anomaly1 test
  • Auditory neuropathy-optic atrophy syndrome1 test
  • Autosomal dominant auditory neuropathy 11 test
  • Autosomal dominant cerebellar ataxia, deafness and narcolepsy1 test
  • Autosomal dominant deafness - onychodystrophy syndrome1 test
  • Autosomal dominant keratitis-ichthyosis-hearing loss syndrome2 tests
  • Autosomal dominant nonsyndromic hearing loss2 tests
  • 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 161 test
  • Autosomal dominant nonsyndromic hearing loss 171 test
  • Autosomal dominant nonsyndromic hearing loss 201 test
  • Autosomal dominant nonsyndromic hearing loss 211 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 271 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 301 test
  • Autosomal dominant nonsyndromic hearing loss 311 test
  • Autosomal dominant nonsyndromic hearing loss 361 test
  • Autosomal dominant nonsyndromic hearing loss 3A1 test
  • Autosomal dominant nonsyndromic hearing loss 3B1 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 491 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 501 test
  • Autosomal dominant nonsyndromic hearing loss 511 test
  • Autosomal dominant nonsyndromic hearing loss 561 test
  • Autosomal dominant nonsyndromic hearing loss 581 test
  • Autosomal dominant nonsyndromic hearing loss 591 test
  • Autosomal dominant nonsyndromic hearing loss 61 test
  • Autosomal dominant nonsyndromic hearing loss 641 test
  • Autosomal dominant nonsyndromic hearing loss 651 test
  • Autosomal dominant nonsyndromic hearing loss 661 test
  • Autosomal dominant nonsyndromic hearing loss 671 test
  • Autosomal dominant nonsyndromic hearing loss 681 test
  • Autosomal dominant nonsyndromic hearing loss 691 test
  • Autosomal dominant nonsyndromic hearing loss 71 test
  • Autosomal dominant nonsyndromic hearing loss 701 test
  • Autosomal dominant nonsyndromic hearing loss 91 test
  • Autosomal dominant optic atrophy plus syndrome1 test
  • Autosomal recessive nonsyndromic hearing loss 1011 test
  • Autosomal recessive nonsyndromic hearing loss 1021 test
  • Autosomal recessive nonsyndromic hearing loss 1031 test
  • Autosomal recessive nonsyndromic hearing loss 1041 test
  • Autosomal recessive nonsyndromic hearing loss 121 test
  • Autosomal recessive nonsyndromic hearing loss 151 test
  • Autosomal recessive nonsyndromic hearing loss 161 test
  • Autosomal recessive nonsyndromic hearing loss 18A1 test
  • Autosomal recessive nonsyndromic hearing loss 18B1 test
  • Autosomal recessive nonsyndromic hearing loss 1A2 tests
  • Autosomal recessive nonsyndromic hearing loss 1B1 test
  • Autosomal recessive nonsyndromic hearing loss 21 test
  • Autosomal recessive nonsyndromic hearing loss 211 test
  • Autosomal recessive nonsyndromic hearing loss 221 test
  • Autosomal recessive nonsyndromic hearing loss 231 test
  • Autosomal recessive nonsyndromic hearing loss 241 test
  • Autosomal recessive nonsyndromic hearing loss 251 test
  • Autosomal recessive nonsyndromic hearing loss 261 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 321 test
  • Autosomal recessive nonsyndromic hearing loss 351 test
  • Autosomal recessive nonsyndromic hearing loss 361 test
  • Autosomal recessive nonsyndromic hearing loss 371 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 441 test
  • Autosomal recessive nonsyndromic hearing loss 451 test
  • Autosomal recessive nonsyndromic hearing loss 481 test
  • Autosomal recessive nonsyndromic hearing loss 491 test
  • Autosomal recessive nonsyndromic hearing loss 51 test
  • Autosomal recessive nonsyndromic hearing loss 531 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 661 test
  • Autosomal recessive nonsyndromic hearing loss 671 test
  • Autosomal recessive nonsyndromic hearing loss 681 test
  • Autosomal recessive nonsyndromic hearing loss 71 test
  • Autosomal recessive nonsyndromic hearing loss 701 test
  • Autosomal recessive nonsyndromic hearing loss 741 test
  • Autosomal recessive nonsyndromic hearing loss 761 test
  • Autosomal recessive nonsyndromic hearing loss 771 test
  • Autosomal recessive nonsyndromic hearing loss 791 test
  • Autosomal recessive nonsyndromic hearing loss 81 test
  • Autosomal recessive nonsyndromic hearing loss 84A1 test
  • Autosomal recessive nonsyndromic hearing loss 84B1 test
  • Autosomal recessive nonsyndromic hearing loss 851 test
  • Autosomal recessive nonsyndromic hearing loss 861 test
  • Autosomal recessive nonsyndromic hearing loss 881 test
  • Autosomal recessive nonsyndromic hearing loss 891 test
  • Autosomal recessive nonsyndromic hearing loss 91 test
  • Autosomal recessive nonsyndromic hearing loss 911 test
  • Autosomal recessive nonsyndromic hearing loss 931 test
  • Autosomal recessive nonsyndromic hearing loss 961 test
  • Autosomal recessive nonsyndromic hearing loss 971 test
  • Autosomal recessive nonsyndromic hearing loss 981 test
  • Baraitser-Winter syndrome1 test
  • Baraitser-Winter syndrome 11 test
  • Baraitser-winter syndrome 21 test
  • Bartter disease type 4A1 test
  • Beta-D-mannosidosis1 test
  • Biotinidase deficiency1 test
  • Bosch-Boonstra-Schaaf optic atrophy syndrome1 test
  • Branchiooculofacial syndrome1 test
  • Branchiootorenal Spectrum Disorders1 test
  • Brown-Vialetto-van Laere syndrome 21 test
  • C3 glomerulonephritis2 tests
  • Camptodactyly, tall stature, and hearing loss syndrome (CATSHL syndrome)1 test
  • Camptodactyly-tall stature-scoliosis-hearing loss syndrome1 test
  • Cardiomyopathy and Deafness1 test
  • CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II1 test
  • CFHR5-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II1 test
  • Charcot-Marie-Tooth disease type 1E1 test
  • Charcot-Marie-Tooth disease type 1F1 test
  • Charcot-Marie-Tooth disease X-linked recessive 21 test
  • Charcot-Marie-Tooth disease X-linked recessive 51 test
  • CHARGE association1 test
  • Chudley-McCullough syndrome1 test
  • Cobalamin C disease1 test
  • Cobalamin deficiency2 tests
  • Combined pituitary hormone deficiencies, genetic form1 test
  • Cone-rod dystrophy and hearing loss1 test
  • Cone-rod dystrophy and hearing loss 11 test
  • Congenital deafness1 test
  • Corneal dystrophy-perceptive deafness syndrome1 test
  • Craniometaphyseal dysplasia, autosomal dominant1 test
  • D-minus hemolytic uremic syndrome (D-HUS)1 test
  • D-plus hemolytic uremic syndrome (D+HUS)1 test
  • Deafness1 test
  • Deafness dystonia syndrome1 test
  • Deafness with labyrinthine aplasia, microtia, and microdontia1 test
  • Deafness, autosomal dominant 39, with dentinogenesis imperfecta 11 test
  • Deafness, autosomal dominant nonsyndromic sensorineural 231 test
  • Deafness, autosomal dominant nonsyndromic sensorineural 241 test
  • Deafness, autosomal recessive 36, without vestibular involvement1 test
  • Deafness, enamel hypoplasia, nail defect syndrome1 test
  • Deafness, without vestibular involvement, autosomal dominant1 test
  • Deafness, X-linked 51 test
  • Deafness-epiphyseal dysplasia-short stature syndrome1 test
  • Deafness-infertility syndrome1 test
  • Deafness-onychodystrophy syndrome1 test
  • Deficiency of alpha-mannosidase1 test
  • Developmental malformations-deafness-dystonia syndrome1 test
  • DFNA 3 Nonsyndromic Hearing Loss and Deafness1 test
  • DFNB 8/10 Nonsyndromic Hearing Loss and Deafness1 test
  • Diabetes-deafness syndrome maternally transmitted1 test
  • DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome1 test
  • Donnai-Barrow syndrome1 test
  • Facial paresis, hereditary congenital, 31 test
  • Familial amyloid nephropathy with urticaria AND deafness1 test
  • Gentamicin response1 test
  • Hearing loss, autosomal dominant 34, with or without inflammation1 test
  • Hearing loss, autosomal dominant 371 test
  • Hearing loss, autosomal dominant 711 test
  • Hearing loss, autosomal dominant 721 test
  • Hearing loss, autosomal dominant 731 test
  • Hearing loss, autosomal dominant 741 test
  • Hearing loss, autosomal dominant 751 test
  • Hearing loss, autosomal dominant 761 test
  • Hearing loss, autosomal dominant 801 test
  • Hearing loss, autosomal recessive1 test
  • Hearing loss, autosomal recessive 1001 test
  • Hearing loss, autosomal recessive 1061 test
  • Hearing loss, autosomal recessive 1071 test
  • Hearing loss, autosomal recessive 1081 test
  • Hearing loss, autosomal recessive 1091 test
  • Hearing loss, autosomal recessive 1101 test
  • Hearing loss, autosomal recessive 1111 test
  • Hearing loss, autosomal recessive 1121 test
  • Hearing loss, autosomal recessive 1131 test
  • Hearing loss, autosomal recessive 1141 test
  • Hearing loss, autosomal recessive 1151 test
  • Hearing loss, autosomal recessive 1161 test
  • Hearing loss, autosomal recessive 1171 test
  • Hearing loss, autosomal recessive 571 test
  • Hearing loss, autosomal recessive 941 test
  • Hearing loss, autosomal recessive 991 test
  • Hearing loss, cisplatin-induced, susceptibility to1 test
  • Hearing loss, X-linked 11 test
  • Hearing loss, X-linked 41 test
  • Hearing loss, X-linked 61 test
  • Hearing Loss/Deafness1 test
  • Hemolytic uremic syndrome, atypical, childhood1 test
  • Hemolytic uremic syndrome, atypical, susceptibility to1 test
  • Hemolytic uremic syndrome, atypical, susceptibility to, 11 test
  • Hemolytic uremic syndrome, atypical, susceptibility to, 71 test
  • Hemolytic-uremic syndrome1 test
  • Hereditary hearing loss and deafness3 tests
  • Hereditary Wilms tumor1 test
  • High myopia-sensorineural deafness syndrome1 test
  • Hirschsprung disease-hearing loss-polydactyly syndrome1 test
  • Huppke-Brendel syndrome1 test
  • Hypoparathyroidism, deafness, renal disease syndrome1 test
  • Hypothyroidism, congenital, nongoitrous, 81 test
  • Isolated hereditary congenital facial paralysis1 test
  • Jervell and Lange-Nielsen syndrome 11 test
  • Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
  • Kabuki syndrome1 test
  • Kanamycin response1 test
  • Keratitis ichthyosis and deafness syndrome1 test
  • Keutel syndrome1 test
  • Leber congenital amaurosis with early-onset deafness1 test
  • Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness1 test
  • Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome1 test
  • Microtia with or without hearing impairment1 test
  • Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis1 test
  • Mitochondrial disease1 test
  • Mitochondrial DNA depletion syndrome1 test
  • Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria1 test
  • Mitochondrial non-syndromic sensorineural hearing loss1 test
  • Neurofibromatosis, type 21 test
  • Nonsyndromic Deafness1 test
  • Nonsyndromic genetic hearing loss2 tests
  • Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive2 tests
  • Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy1 test
  • Otofaciocervical syndrome1 test
  • Palmoplantar keratoderma-deafness syndrome2 tests
  • Pendred syndrome1 test
  • Peroxisome biogenesis disorder1 test
  • Perrault syndrome1 test
  • Perrault syndrome 11 test
  • Perrault syndrome 21 test
  • Perrault syndrome 31 test
  • Perrault syndrome 41 test
  • Perrault syndrome 51 test
  • Perrault syndrome 61 test
  • Pfeiffer syndrome1 test
  • Pfeiffer syndrome type 11 test
  • Pfeiffer syndrome type 21 test
  • PHARC syndrome1 test
  • Pili torti-deafness syndrome1 test
  • Progressive deafness with stapes fixation1 test
  • Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome1 test
  • Rare genetic deafness1 test
  • Renal tubular acidosis 31 test
  • Renal tubular acidosis with progressive nerve deafness1 test
  • Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss1 test
  • Riboflavin transporter deficiency1 test
  • Sensorineural deafness with hypertrophic cardiomyopathy1 test
  • Sensorineural deafness with mild renal dysfunction1 test
  • Sensorineural hearing loss disorder1 test
  • Siddiqi syndrome1 test
  • Sinoatrial node dysfunction and deafness1 test
  • Split hand-foot malformation 1 with sensorineural hearing loss1 test
  • Stapes ankylosis with broad thumbs and toes1 test
  • Stickler syndrome1 test
  • Streptomycin response1 test
  • Syndromic genetic hearing loss1 test
  • Temtamy preaxial brachydactyly syndrome1 test
  • Thrombotic microangiopathy2 tests
  • Thrombotic thrombocytopenic purpura1 test
  • Tobramycin response1 test
  • Treacher Collins syndrome1 test
  • Treacher Collins syndrome 11 test
  • Upshaw-Schulman syndrome2 tests
  • Usher syndrome2 tests
  • Usher syndrome type 12 tests
  • Usher syndrome type 1B2 tests
  • Usher syndrome type 1C2 tests
  • Usher syndrome type 1D2 tests
  • Usher syndrome type 1E1 test
  • Usher syndrome type 1F2 tests
  • Usher syndrome type 1G2 tests
  • Usher syndrome type 1H1 test
  • Usher syndrome type 22 tests
  • Usher syndrome type 2A1 test
  • Usher syndrome type 2C1 test
  • Usher syndrome type 2D1 test
  • Usher syndrome type 32 tests
  • Usher syndrome type 3A2 tests
  • Usher syndrome type 3B1 test
  • Usher syndrome, type IIC, GPR98/PDZD7 digenic1 test
  • Waardenburg syndrome1 test
  • Waardenburg syndrome type 11 test
  • Waardenburg syndrome type 21 test
  • Waardenburg syndrome type 31 test
  • Waardenburg syndrome type 4A1 test
  • Waardenburg syndrome type 4B1 test
  • Waardenburg syndrome type 4C1 test
  • Wolfram syndrome1 test
  • Wolfram syndrome 11 test
  • Wolfram syndrome 21 test
  • Wolfram syndrome, mitochondrial form1 test
  • Woodhouse-Sakati syndrome1 test
  • X-linked complicated corpus callosum dysgenesis1 test
  • X-linked deafness1 test
  • X-linked mixed hearing loss with perilymphatic gusher1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Sequence Analysis

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 16D0966193, Expiration date: 2025-06-18
  • JCAHO, Number: Lab CLIA: 16D0966193, Expiration date: 2025-05-12

Licenses

  • CA - California Department of Public Health CDPH, Number: CDS-90006201, Expiration date: 2024-03-30
  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 1679, Effective date: 2018-07-01 Non-expiring
  • PA - Pennsylvania Department of Health PADOH, Number: 034100, 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.