Synlab MVZ Humane Genetik München

Personnel

Director: Claudia Nevinny-Stickel-Hinzpeter, Lab Director
Phone: +49 895486290
Fax: +49 89548629243
Email: claudia.nevinny@synlab.com
Claudia Bayerl, Laboratory Contact
Phone: +49 895486290
Fax: +49 89548629243
Email: claudia.bayerl@synlab.com
Birgit Becker, Laboratory Contact
Phone: +49 895486290
Email: Birgit.Becker@synlab.com
Sonja Bingemann, Laboratory Contact
Phone: +49 895486290
Email: sonja.bingemann@synlab.com
Stefanie Bug, Laboratory Contact
Phone: +49 895486290
Paivi Forsblom, Laboratory Contact
Phone: +49 5486290
Email: paeivi.forsblom@synlab.com

Conditions and tests

96 conditions/phenotypes with 75 tests
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Aarskog syndrome1 test
Achondroplasia1 test
Adult-onset autosomal dominant demyelinating leukodystrophy1 test
alpha Thalassemia1 test
Alpha-1-antitrypsin deficiency1 test
Alport syndrome1 test
Anemia, nonspherocytic hemolytic, due to G6PD deficiency1 test
Angelman syndrome1 test
Arrhythmogenic right ventricular cardiomyopathy1 test
Autosomal dominant optic atrophy classic form1 test
Autosomal dominant polycystic kidney disease1 test
Beckwith-Wiedemann syndrome1 test
beta Thalassemia1 test
Brugada syndrome 11 test
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
Charcot-Marie-Tooth disease, type 2A1 test
Charcot-Marie-Tooth disease, type I1 test
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
Colorectal cancer, hereditary nonpolyposis, type 21 test
Crigler-Najjar syndrome1 test
Dilated cardiomyopathy 1A1 test
Duchenne muscular dystrophy1 test
Ehlers-Danlos syndrome1 test
Fabry disease1 test
Familial amyloid nephropathy with urticaria AND deafness1 test
Familial Mediterranean fever1 test
Familial multiple polyposis syndrome1 test
Familial renal glucosuria1 test
Fragile X syndrome1 test
Gilbert syndrome1 test
Hemochromatosis type 11 test
Hemochromatosis type 2A1 test
Hemochromatosis type 2B1 test
Hemochromatosis type 31 test
Hemochromatosis type 41 test
Hereditary factor IX deficiency disease1 test
Hereditary factor VIII deficiency disease1 test
Hereditary liability to pressure palsies1 test
Hereditary pancreatitis1 test
Huntington disease1 test
Hypercholesterolemia, familial, 11 test
Hyperimmunoglobulin D with periodic fever1 test
Hyperinsulinemic hypoglycemia, familial, 11 test
Hyperinsulinemic hypoglycemia, familial, 21 test
Hyperinsulinism due to glucokinase deficiency1 test
Hyperinsulinism-hyperammonemia syndrome1 test
Hypertrophic cardiomyopathy 11 test
Hypertrophic cardiomyopathy 21 test
Hypertrophic cardiomyopathy 41 test
Hypertrophic cardiomyopathy 71 test
Hypochondroplasia1 test
Hypogonadotropic hypogonadism 1 with or without anosmia1 test
Hypogonadotropic hypogonadism 2 with or without anosmia1 test
Hypoparathyroidism, deafness, renal disease syndrome1 test
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
Kennedy disease1 test
Leber optic atrophy1 test
Li-Fraumeni syndrome1 test
Loeys-Dietz syndrome 11 test
Long QT syndrome 11 test
Long QT syndrome 21 test
Long QT syndrome 31 test
Long QT syndrome 51 test
Long QT syndrome 61 test
Marfan syndrome1 test
Maturity onset diabetes mellitus in young1 test
Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
MERRF syndrome1 test
Mitochondrial DNA-Associated Leigh Syndrome and NARP1 test
Multiple endocrine neoplasia, type 11 test
Multiple endocrine neoplasia, type 21 test
Myotonic dystrophy type 21 test
Neonatal diabetes mellitus1 test
Neurofibromatosis, type 11 test
Noonan syndrome 11 test
Noonan syndrome 41 test
Noonan syndrome with multiple lentigines1 test
Obesity1 test
Osteogenesis imperfecta type I1 test
Phenylketonuria1 test
Prader-Willi syndrome1 test
Progressive external ophthalmoplegia1 test
Rett syndrome1 test
Short QT syndrome type 11 test
Short QT syndrome type 21 test
Short stature due to partial GHR deficiency1 test
Silver-Russell syndrome 11 test
Sotos syndrome1 test
Spinal muscular atrophy1 test
Statin causing adverse effect in therapeutic use1 test
Steinert myotonic dystrophy syndrome1 test
Thanatophoric dysplasia type 11 test
TNF receptor-associated periodic fever syndrome (TRAPS)1 test
Velocardiofacial syndrome1 test
Von Hippel-Lindau syndrome1 test
Wilson disease1 test

List of services

This lab has no services.

List of certifications/licenses

Certifications

DAkkS, Number: D-ML-13225-02-00, Expiration date: 2017-11-01

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.