GTR Home > Laboratories > Synlab MVZ Humane Genetik München

Synlab MVZ Humane Genetik München

GTR Lab ID: 260566, Last updated:2015-04-28

Personnel

Conditions and tests

  • 21-hydroxylase deficiency1 test
  • Aarskog syndrome1 test
  • Achondroplasia1 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
  • Barakat syndrome1 test
  • Beckwith-Wiedemann syndrome1 test
  • beta Thalassemia1 test
  • Brugada syndrome 11 test
  • Bulbo-spinal atrophy X-linked1 test
  • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy1 test
  • Charcot-Marie-Tooth disease, type 2A1 test
  • Charcot-Marie-Tooth disease, type I1 test
  • Crigler-Najjar syndrome1 test
  • Dilated cardiomyopathy 1A1 test
  • Dominant hereditary optic atrophy1 test
  • Duchenne muscular dystrophy1 test
  • Ehlers-Danlos syndrome1 test
  • Fabry's disease1 test
  • Familial amyloid nephropathy with urticaria AND deafness1 test
  • Familial hypercholesterolemia1 test
  • Familial hypertrophic cardiomyopathy 11 test
  • Familial hypertrophic cardiomyopathy 21 test
  • Familial hypertrophic cardiomyopathy 41 test
  • Familial hypertrophic cardiomyopathy 71 test
  • Familial Mediterranean fever1 test
  • Familial multiple polyposis syndrome1 test
  • Familial renal glucosuria1 test
  • Fragile X syndrome1 test
  • Gilbert's 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's chorea1 test
  • Hyperimmunoglobulin D with periodic fever1 test
  • Hyperinsulinemic hypoglycemia familial 31 test
  • Hyperinsulinism-hyperammonemia syndrome1 test
  • Hypochondroplasia1 test
  • Islet cell hyperplasia1 test
  • Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
  • Kallmann syndrome 11 test
  • Kallmann syndrome 21 test
  • Leber's optic atrophy1 test
  • LEOPARD syndrome1 test
  • Leukodystrophy, adult-onset, autosomal dominant1 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
  • Lynch syndrome II1 test
  • Marfan's syndrome1 test
  • Maturity onset diabetes mellitus in young1 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Mitochondrial DNA-Associated Leigh Syndrome and NARP1 test
  • Multiple endocrine neoplasia, type 11 test
  • Multiple endocrine neoplasia, type 21 test
  • Myoclonus with epilepsy with ragged red fibers1 test
  • Myotonic dystrophy type 21 test
  • Neonatal diabetes mellitus1 test
  • Neurofibromatosis, type 11 test
  • Noonan syndrome 11 test
  • Noonan syndrome 41 test
  • Obesity1 test
  • Osteogenesis imperfecta type I1 test
  • Persistent hyperinsulinemic hypoglycemia of infancy1 test
  • Phenylketonuria1 test
  • Polycystic kidney disease, autosomal dominant1 test
  • Prader-Willi syndrome1 test
  • Progressive external ophthalmoplegia1 test
  • Rett's disorder1 test
  • Russell-Silver syndrome1 test
  • Short QT syndrome 11 test
  • Short QT syndrome 21 test
  • Short stature, idiopathic, autosomal1 test
  • Shprintzen syndrome1 test
  • Sotos syndrome 11 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
  • Von Hippel-Lindau syndrome1 test
  • Wilson's 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

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