U.S. flag

An official website of the United States government

GTR Home > Laboratories > Synlab MVZ Humane Genetik München

Synlab MVZ Humane Genetik München

GTR Lab ID: 260566, Last updated:2023-05-22
Annual Review past due read more


Conditions and tests

  • 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
  • Angiokeratoma corporis diffusum1 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
  • 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


  • 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.