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GTR Home > Laboratories > Labor Dr. Wisplinghoff

Labor Dr. Wisplinghoff

GTR Lab ID: 506159, Last updated:2023-05-26

Personnel

  • Director: Ulrich Zechner, PhD, Lab Director
    Phone: +(49)-221-940505203
    Fax: +(49)-221-940505412
    Email: U.Zechner@wisplinghoff.de
  • Sabrina Sauer, PhD, Staff
    Phone: +(49)-221-940505682
    Fax: +(49)-221-940505412
    Email: S.Sauer@wisplinghoff.de
  • Lars-Erik Wehner, MD, Genetic Counselor
    Phone: +(49)-221-940505845
    Email: L.Wehner@wisplinghoff.de
  • Kurt-Peter Wisplinghoff, PhD, Medical Director

Conditions and tests

  • 3-methylglutaconic aciduria type 51 test
  • 46,XY sex reversal 11 test
  • Acute intermittent porphyria1 test
  • Adams-Oliver syndrome 11 test
  • Adult-onset foveomacular vitelliform dystrophy1 test
  • Alagille syndrome due to a JAG1 point mutation1 test
  • Alexander disease1 test
  • alpha Thalassemia1 test
  • Alpha-1-antitrypsin deficiency1 test
  • Alzheimer disease 31 test
  • Alzheimer disease 41 test
  • Alzheimer disease type 11 test
  • Amyotrophic lateral sclerosis type 11 test
  • Androgen resistance syndrome1 test
  • Angelman syndrome1 test
  • Angelman syndrome-like1 test
  • Arrhythmogenic cardiomyopathy with wooly hair and keratoderma1 test
  • Arrhythmogenic right ventricular dysplasia 101 test
  • Arrhythmogenic right ventricular dysplasia 111 test
  • Arrhythmogenic right ventricular dysplasia 121 test
  • Arrhythmogenic right ventricular dysplasia 51 test
  • Arrhythmogenic right ventricular dysplasia 81 test
  • Arrhythmogenic right ventricular dysplasia 91 test
  • Arrhythmogenic right ventricular dysplasia, familial, 71 test
  • Arterial tortuosity syndrome1 test
  • Autosomal dominant hypocalcemia 11 test
  • Autosomal dominant nonsyndromic hearing loss 171 test
  • Autosomal dominant polycystic kidney disease1 test
  • Autosomal recessive inherited pseudoxanthoma elasticum1 test
  • Autosomal recessive nonsyndromic hearing loss 1A1 test
  • Autosomal recessive severe congenital neutropenia due to CSF3R deficiency1 test
  • beta Thalassemia1 test
  • Brunner syndrome1 test
  • Cardio-facio-cutaneous syndrome1 test
  • Cardiomyopathy, dilated, 1AA, with or without LVNC1 test
  • Cardiomyopathy, dilated, 1LL1 test
  • Cardiomyopathy, dilated, 1MM1 test
  • Cardiomyopathy, dilated, 2c1 test
  • Cardiomyopathy, dilated, 2D1 test
  • Cardiomyopathy, dilated, 2E1 test
  • Carnitine palmitoyltransferase II deficiency1 test
  • Catecholaminergic polymorphic ventricular tachycardia 11 test
  • Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
  • Cerebral cavernous malformation 11 test
  • Cerebral cavernous malformation 21 test
  • Cerebral cavernous malformation 31 test
  • Coffin-Lowry syndrome1 test
  • Colorectal cancer, hereditary nonpolyposis, type 21 test
  • Congenital adrenal hypoplasia, X-linked1 test
  • Congenital afibrinogenemia1 test
  • Congenital myotonia, autosomal dominant form1 test
  • Congenital myotonia, autosomal recessive form1 test
  • Costello syndrome1 test
  • Crigler-Najjar syndrome1 test
  • Crouzon syndrome1 test
  • Crouzon syndrome-acanthosis nigricans syndrome1 test
  • Cystic fibrosis1 test
  • Deficiency of butyrylcholinesterase1 test
  • Developmental and epileptic encephalopathy, 21 test
  • Developmental and epileptic encephalopathy, 91 test
  • Diabetes insipidus, nephrogenic, autosomal1 test
  • Diabetes insipidus, nephrogenic, X-linked1 test
  • Dilated cardiomyopathy 1A2 tests
  • Dilated cardiomyopathy 1BB1 test
  • Dilated cardiomyopathy 1C1 test
  • Dilated cardiomyopathy 1CC1 test
  • Dilated cardiomyopathy 1D1 test
  • Dilated cardiomyopathy 1DD1 test
  • Dilated cardiomyopathy 1E1 test
  • Dilated cardiomyopathy 1EE1 test
  • Dilated cardiomyopathy 1FF1 test
  • Dilated cardiomyopathy 1G1 test
  • Dilated cardiomyopathy 1HH1 test
  • Dilated cardiomyopathy 1I1 test
  • Dilated cardiomyopathy 1II1 test
  • Dilated cardiomyopathy 1JJ1 test
  • Dilated cardiomyopathy 1KK1 test
  • Dilated cardiomyopathy 1L1 test
  • Dilated cardiomyopathy 1M1 test
  • Dilated cardiomyopathy 1NN1 test
  • Dilated cardiomyopathy 1O1 test
  • Dilated cardiomyopathy 1P1 test
  • Dilated cardiomyopathy 1R1 test
  • Dilated cardiomyopathy 1S1 test
  • Dilated cardiomyopathy 1U1 test
  • Dilated cardiomyopathy 1V1 test
  • Dilated cardiomyopathy 1W1 test
  • Dilated cardiomyopathy 1X1 test
  • Dilated cardiomyopathy 1Y1 test
  • Dilated cardiomyopathy 1Z1 test
  • Dilated cardiomyopathy 3B1 test
  • DK1-congenital disorder of glycosylation1 test
  • Early-onset generalized limb-onset dystonia1 test
  • Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant2 tests
  • Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive2 tests
  • Ehlers-Danlos syndrome, type 41 test
  • Episodic pain syndrome, familial, 21 test
  • Fabry disease1 test
  • Familial adenomatous polyposis 12 tests
  • Familial amyloid nephropathy with urticaria AND deafness1 test
  • Familial amyloid neuropathy1 test
  • Familial cancer of breast1 test
  • Familial episodic pain syndrome with predominantly lower limb involvement1 test
  • Familial hypocalciuric hypercalcemia 11 test
  • Familial Mediterranean fever1 test
  • Fragile X syndrome1 test
  • Fragile X-associated tremor/ataxia syndrome1 test
  • Frontotemporal dementia1 test
  • Generalized epilepsy with febrile seizures plus, type 21 test
  • Gilbert syndrome1 test
  • Glomuvenous malformation1 test
  • Glucose-6-phosphate transport defect1 test
  • Glycogen storage disease due to glucose-6-phosphatase deficiency type IA1 test
  • Glycogen storage disease, type II1 test
  • Glycogen storage disease, type V1 test
  • Greig cephalopolysyndactyly syndrome1 test
  • Hb SS disease1 test
  • Hemochromatosis type 11 test
  • Hemochromatosis type 2A1 test
  • Hemochromatosis type 2B1 test
  • Hemochromatosis type 31 test
  • Hemochromatosis type 41 test
  • Hereditary antithrombin deficiency1 test
  • Hereditary diffuse gastric adenocarcinoma1 test
  • Hereditary fructosuria1 test
  • Hereditary hyperferritinemia with congenital cataracts1 test
  • Hereditary neutrophilia1 test
  • Hereditary pancreatitis1 test
  • Histiocytic medullary reticulosis1 test
  • Huntington disease1 test
  • Hyper-IgE recurrent infection syndrome 1, autosomal dominant1 test
  • Hypercholesterolemia, autosomal dominant, 31 test
  • Hypercholesterolemia, autosomal dominant, type B1 test
  • Hypercholesterolemia, familial, 11 test
  • Hyperimmunoglobulin D with periodic fever1 test
  • Hypertrophic cardiomyopathy 11 test
  • Hypertrophic cardiomyopathy 101 test
  • Hypertrophic cardiomyopathy 181 test
  • Hypertrophic cardiomyopathy 21 test
  • Hypertrophic cardiomyopathy 262 tests
  • Hypertrophic cardiomyopathy 41 test
  • Hypertrophic cardiomyopathy 71 test
  • Hypertrophic cardiomyopathy 81 test
  • Hypogonadotropic hypogonadism 1 with or without anosmia1 test
  • Hypogonadotropic hypogonadism 2 with or without anosmia2 tests
  • Hypogonadotropic hypogonadism 3 with or without anosmia1 test
  • Hypogonadotropic hypogonadism 4 with or without anosmia1 test
  • Hypohidrotic X-linked ectodermal dysplasia1 test
  • Inflammatory bowel disease 11 test
  • Jackson-Weiss syndrome1 test
  • Jervell and Lange-Nielsen syndrome 11 test
  • Jervell and Lange-Nielsen syndrome 21 test
  • Keutel syndrome1 test
  • Kindler syndrome1 test
  • Kugelberg-Welander disease1 test
  • L-ferritin deficiency1 test
  • Langer mesomelic dysplasia syndrome1 test
  • Legius syndrome1 test
  • Leri-Weill dyschondrosteosis1 test
  • Leydig cell agenesis1 test
  • Long QT syndrome 11 test
  • Long QT syndrome 21 test
  • Long QT syndrome 31 test
  • Long QT syndrome 51 test
  • Lynch syndrome 11 test
  • Lynch syndrome 41 test
  • Lynch syndrome 51 test
  • Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss1 test
  • Majeed syndrome1 test
  • Mannose-binding lectin deficiency1 test
  • Maturity-onset diabetes of the young type 11 test
  • Maturity-onset diabetes of the young type 111 test
  • Maturity-onset diabetes of the young type 141 test
  • Maturity-onset diabetes of the young type 21 test
  • Maturity-onset diabetes of the young type 31 test
  • Maturity-onset diabetes of the young type 41 test
  • Maturity-onset diabetes of the young type 61 test
  • Maturity-onset diabetes of the young type 71 test
  • Maturity-onset diabetes of the young type 91 test
  • Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 11 test
  • Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 21 test
  • Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 31 test
  • Mucopolysaccharidosis type 11 test
  • Muenke syndrome1 test
  • Multiple endocrine neoplasia type 41 test
  • Multiple endocrine neoplasia, type 11 test
  • Multiple endocrine neoplasia, type 2a1 test
  • Multiple endocrine neoplasia, type 2b1 test
  • Muscle AMP deaminase deficiency1 test
  • Myopathy, centronuclear, 51 test
  • Neonatal severe primary hyperparathyroidism1 test
  • Neuroferritinopathy1 test
  • Neurofibromatosis, type 11 test
  • Neurofibromatosis, type 21 test
  • Neurofibromatosis-Noonan syndrome1 test
  • Neuropathy, hereditary sensory, type 1F1 test
  • none1 test
  • Ovarian dysgenesis 11 test
  • Ovarian dysgenesis 21 test
  • Paramyotonia congenita of Von Eulenburg1 test
  • Paroxysmal extreme pain disorder1 test
  • Partial hypoxanthine-guanine phosphoribosyltransferase deficiency1 test
  • Pendred syndrome1 test
  • Peutz-Jeghers syndrome1 test
  • Pfeiffer syndrome1 test
  • Prader-Willi syndrome1 test
  • Premature ovarian failure 11 test
  • Primary familial polycythemia due to EPO receptor mutation1 test
  • Prolidase deficiency1 test
  • Proteasome-associated autoinflammatory syndrome 11 test
  • Pulmonary hypertension, primary, 11 test
  • Renal cysts and diabetes syndrome1 test
  • Rett syndrome1 test
  • Saethre-Chotzen syndrome1 test
  • Schinzel-Giedion syndrome1 test
  • Selective pituitary resistance to thyroid hormone1 test
  • SHOX-related short stature1 test
  • Slow acetylator due to N-acetyltransferase enzyme variant1 test
  • Sotos syndrome1 test
  • Spinal muscular atrophy, type II1 test
  • Spinal muscular atrophy, type IV1 test
  • Spinocerebellar ataxia type 61 test
  • Steinert myotonic dystrophy syndrome1 test
  • Telangiectasia, hereditary hemorrhagic, type 11 test
  • Telangiectasia, hereditary hemorrhagic, type 21 test
  • Thiopurine S-methyltransferase deficiency1 test
  • Thrombophilia due to protein C deficiency, autosomal dominant1 test
  • Thrombophilia due to protein C deficiency, autosomal recessive1 test
  • Thrombophilia due to protein S deficiency, autosomal dominant1 test
  • Thrombophilia due to protein S deficiency, autosomal recessive1 test
  • Thyroid hormone resistance, generalized, autosomal dominant1 test
  • Thyroid hormone resistance, generalized, autosomal recessive1 test
  • TNF receptor-associated periodic fever syndrome (TRAPS)1 test
  • Torsion dystonia 61 test
  • Very long chain acyl-CoA dehydrogenase deficiency1 test
  • Vitelliform macular dystrophy 21 test
  • Vitelliform macular dystrophy 41 test
  • Vitelliform macular dystrophy 51 test
  • Von Hippel-Lindau syndrome1 test
  • Warfarin response1 test
  • Weaver syndrome1 test
  • Werdnig-Hoffmann disease1 test
  • Wilson disease1 test
  • Wiskott-Aldrich syndrome1 test
  • X-linked agammaglobulinemia1 test
  • X-linked Opitz G/BBB syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Genetic counseling
  • Whole Exome Sequencing

List of certifications/licenses

Certifications

  • ISO15189, Number: D-ML-13062-01-00

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.