U.S. flag

An official website of the United States government

GTR Home > Laboratories > GGA - Galil Genetic Analysis

GGA - Galil Genetic Analysis

GTR Lab ID: 320113, Last updated:2023-05-08
Annual Review past due read more

Personnel

Conditions and tests

  • 3 beta-Hydroxysteroid dehydrogenase deficiency1 test
  • Aarskog syndrome1 test
  • Abetalipoproteinaemia1 test
  • Achromatopsia 21 test
  • Acquired long QT syndrome1 test
  • Adrenoleukodystrophy1 test
  • Alpha-1-antitrypsin deficiency1 test
  • Alternating hemiplegia of childhood 11 test
  • Alzheimer disease 41 test
  • Andersen Tawil syndrome1 test
  • Androgen resistance syndrome1 test
  • Angelman syndrome1 test
  • Arrhythmogenic right ventricular cardiomyopathy4 tests
  • Arrhythmogenic right ventricular dysplasia 101 test
  • Arrhythmogenic right ventricular dysplasia 111 test
  • Arrhythmogenic right ventricular dysplasia 121 test
  • Arrhythmogenic right ventricular dysplasia 81 test
  • Arrhythmogenic right ventricular dysplasia 91 test
  • Asphyxiating thoracic dystrophy 21 test
  • Asphyxiating thoracic dystrophy 31 test
  • Ataxia-telangiectasia syndrome1 test
  • Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly1 test
  • Autism spectrum disorder1 test
  • Autosomal recessive limb-girdle muscular dystrophy type 2A1 test
  • Autosomal recessive limb-girdle muscular dystrophy type 2D1 test
  • Bardet-Biedl syndrome 11 test
  • Bardet-Biedl syndrome 121 test
  • Bardet-Biedl syndrome 21 test
  • Bardet-Biedl syndrome 31 test
  • Bardet-Biedl syndrome 41 test
  • Bardet-Biedl syndrome 51 test
  • Bardet-Biedl syndrome 71 test
  • Bartter disease type 11 test
  • Bartter disease type 21 test
  • Bartter disease type 31 test
  • Beckwith-Wiedemann syndrome1 test
  • Breast-ovarian cancer, familial, susceptibility to, 11 test
  • Breast-ovarian cancer, familial, susceptibility to, 21 test
  • Brugada syndrome 51 test
  • Cardiomyopathy1 test
  • Carney complex1 test
  • Catecholaminergic polymorphic ventricular tachycardia 11 test
  • Catecholaminergic polymorphic ventricular tachycardia 21 test
  • Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 11 test
  • Childhood apraxia of speech1 test
  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
  • Congenital long QT syndrome2 tests
  • Congenital microvillous atrophy1 test
  • Congenital myopathy with fiber type disproportion1 test
  • Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome1 test
  • Deficiency of steroid 11-beta-monooxygenase1 test
  • Developmental and epileptic encephalopathy, 11 test
  • Diabetes mellitus, transient neonatal, 21 test
  • Diaphyseal dysplasia1 test
  • Ehlers-Danlos syndrome1 test
  • Fabry disease, cardiac variant1 test
  • Familial adenomatous polyposis 11 test
  • Familial adenomatous polyposis 21 test
  • Familial hypercholesterolemia3 tests
  • Familial hypocalciuric hypercalcemia 11 test
  • Familial medullary thyroid carcinoma1 test
  • Familial thoracic aortic aneurysm and aortic dissection4 tests
  • Generalized juvenile polyposis/juvenile polyposis coli1 test
  • Glucocorticoid deficiency with achalasia1 test
  • Hereditary pheochromocytoma-paraganglioma4 tests
  • Hyper-IgE recurrent infection syndrome 1, autosomal dominant1 test
  • Hypertrophic cardiomyopathy 111 test
  • Infantile cortical hyperostosis1 test
  • Li-Fraumeni syndrome1 test
  • Li-Fraumeni syndrome 21 test
  • Loeys-Dietz syndrome1 test
  • Lynch syndrome4 tests
  • Malignant hyperthermia of anesthesia2 tests
  • Malignant hyperthermia, susceptibility to, 51 test
  • Metachromatic leukodystrophy1 test
  • Multiple endocrine neoplasia, type 11 test
  • Multiple endocrine neoplasia, type 21 test
  • Neurofibromatosis, type 21 test
  • Neuronopathy, distal hereditary motor, type 5A1 test
  • Noonan syndrome 71 test
  • Peutz-Jeghers syndrome1 test
  • Polyglandular autoimmune syndrome, type 11 test
  • Primary familial hypertrophic cardiomyopathy8 tests
  • Progressive familial intrahepatic cholestasis type 11 test
  • Progressive familial intrahepatic cholestasis type 21 test
  • PTEN hamartoma tumor syndrome with granular cell tumor1 test
  • Retinoblastoma1 test
  • Seizures, benign familial infantile, 31 test
  • Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis1 test
  • Somatotroph adenoma1 test
  • Sphingomyelin/cholesterol lipidosis1 test
  • Spongy degeneration of central nervous system1 test
  • Tangier disease1 test
  • Telangiectasia, hereditary hemorrhagic, type 21 test
  • TNF receptor-associated periodic fever syndrome (TRAPS)1 test
  • Tuberous sclerosis 11 test
  • Tuberous sclerosis 21 test
  • Von Hippel-Lindau syndrome1 test
  • Wilms tumor 11 test
  • X-linked severe combined immunodeficiency1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

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.