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GTR Home > Laboratories > Laboratory for Molecular Diagnostics

Laboratory for Molecular Diagnostics

GTR Lab ID: 222598, Last updated:2023-10-05

Personnel

  • Director: Mato Nagel, MD, Medical Director
    Phone: +49 3576287922
    Fax: +49 3576287944
    Email: nagel@moldiag.de
  • Mandy Benke, Lab Director
    Phone: +49 3576215522
    Fax: +49 3576215524
    Email: labor@moldiag.de

Conditions and tests

  • 11p partial monosomy syndrome1 test
  • Abetalipoproteinaemia1 test
  • ABri amyloidosis1 test
  • Achondroplasia1 test
  • ACTH-independent macronodular adrenal hyperplasia 21 test
  • Adenine phosphoribosyltransferase deficiency1 test
  • Age-related macular degeneration1 test
  • Alport syndrome1 test
  • Alstrom syndrome1 test
  • Alzheimer disease 21 test
  • Alzheimer disease 41 test
  • Amyloidogenic transthyretin amyloidosis1 test
  • Analbuminemia1 test
  • Aniridia 11 test
  • Apolipoprotein c-III deficiency1 test
  • Apparent mineralocorticoid excess1 test
  • Argininosuccinate lyase deficiency1 test
  • Arterial calcification, generalized, of infancy, 21 test
  • Arthrogryposis, renal dysfunction, and cholestasis 11 test
  • Arthrogryposis, renal dysfunction, and cholestasis 21 test
  • Ateleiotic dwarfism2 tests
  • Atrial fibrillation, familial, 71 test
  • Atypical hemolytic-uremic syndrome1 test
  • Atypical hemolytic-uremic syndrome with B factor anomaly1 test
  • Atypical hemolytic-uremic syndrome with C3 anomaly1 test
  • Atypical hemolytic-uremic syndrome with I factor anomaly2 tests
  • Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly1 test
  • Atypical hemolytic-uremic syndrome with thrombomodulin anomaly1 test
  • Autoinflammatory syndrome, familial, Behcet-like1 test
  • Autosomal dominant Alport syndrome1 test
  • Autosomal dominant distal renal tubular acidosis1 test
  • Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome1 test
  • Autosomal dominant hypophosphatemic rickets1 test
  • Autosomal dominant isolated somatotropin deficiency1 test
  • Autosomal dominant nonsyndromic hearing loss 171 test
  • Autosomal dominant nonsyndromic hearing loss 61 test
  • Autosomal dominant optic atrophy classic form1 test
  • Autosomal dominant osteopetrosis 11 test
  • Autosomal dominant pseudohypoaldosteronism type 11 test
  • Autosomal recessive Alport syndrome1 test
  • Autosomal recessive distal renal tubular acidosis1 test
  • Autosomal recessive hypophosphatemic bone disease3 tests
  • Autosomal recessive nonsyndromic hearing loss 41 test
  • Autosomal recessive polycystic kidney disease2 tests
  • Autosomal recessive proximal renal tubular acidosis1 test
  • Autosomal recessive pseudohypoaldosteronism type 11 test
  • Bardet-Biedl syndrome1 test
  • Bardet-Biedl syndrome 11 test
  • Bardet-Biedl syndrome 101 test
  • Bardet-Biedl syndrome 111 test
  • Bardet-Biedl syndrome 121 test
  • Bardet-Biedl syndrome 131 test
  • Bardet-Biedl syndrome 141 test
  • Bardet-Biedl syndrome 151 test
  • Bardet-Biedl syndrome 161 test
  • Bardet-Biedl syndrome 171 test
  • Bardet-Biedl syndrome 181 test
  • Bardet-Biedl syndrome 191 test
  • Bardet-Biedl syndrome 21 test
  • Bardet-Biedl syndrome 31 test
  • Bardet-Biedl syndrome 41 test
  • Bardet-Biedl syndrome 51 test
  • Bardet-Biedl syndrome 61 test
  • Bardet-Biedl syndrome 71 test
  • Bardet-Biedl syndrome 81 test
  • Bardet-Biedl syndrome 91 test
  • Bartter disease type 11 test
  • Bartter disease type 21 test
  • Bartter disease type 31 test
  • Bartter disease type 4A1 test
  • Bartter disease type 4B1 test
  • Bernard-Soulier syndrome type C1 test
  • Bernard-Soulier syndrome, type A1 test
  • Bernard-Soulier syndrome, type B1 test
  • BLOOD GROUP--FROESE1 test
  • Brachydactyly-arterial hypertension syndrome1 test
  • Brain small vessel disease 1 with or without ocular anomalies2 tests
  • Branchiootic syndrome 31 test
  • Branchiootorenal syndrome 11 test
  • Branchiootorenal syndrome 21 test
  • Bronchiectasis with or without elevated sweat chloride 12 tests
  • Bronchiectasis with or without elevated sweat chloride 21 test
  • Bronchiectasis with or without elevated sweat chloride 31 test
  • Brunner syndrome1 test
  • C1Q deficiency1 test
  • Calcium oxalate nephrolithiasis1 test
  • Capillary infantile hemangioma1 test
  • Carnitine palmitoyl transferase II deficiency, severe infantile form1 test
  • Caroli disease1 test
  • Carotid intimal medial thickness 11 test
  • Cataract with late-onset corneal dystrophy1 test
  • Cerebral amyloid angiopathy, APP-related1 test
  • CFH-Related Dense Deposit Disease / Membranoproliferative Glomerulonephritis Type II1 test
  • Chondrodysplasia Blomstrand type1 test
  • Chronic infantile neurological, cutaneous and articular syndrome1 test
  • CIDEC-related familial partial lipodystrophy1 test
  • Citrin deficiency1 test
  • Citrullinemia type I1 test
  • Citrullinemia type II1 test
  • Coenzyme Q10 deficiency, primary, 11 test
  • Coenzyme Q10 deficiency, primary, 31 test
  • Colorectal cancer, hereditary nonpolyposis, type 21 test
  • Complement component 2 deficiency1 test
  • Complement component 3 deficiency1 test
  • Complement component 4a deficiency1 test
  • Complement component 5 deficiency1 test
  • Complement component 9 deficiency1 test
  • Congenital adrenal hypoplasia, X-linked1 test
  • Congenital afibrinogenemia1 test
  • Congenital anomalies of kidney and urinary tract 11 test
  • Congenital central hypoventilation1 test
  • Congenital generalized lipodystrophy type 11 test
  • Congenital generalized lipodystrophy type 21 test
  • Congenital glucose-galactose malabsorption1 test
  • Congenital isolated adrenocorticotropic hormone deficiency1 test
  • Congenital lactase deficiency1 test
  • Congenital muscular dystrophy1 test
  • Corticosterone 18-monooxygenase deficiency1 test
  • Cystinuria1 test
  • Dalmatian hypouricemia1 test
  • Deafness-encephaloneuropathy-obesity-valvulopathy syndrome1 test
  • Deficiency of ferroxidase1 test
  • Deficiency of steroid 11-beta-monooxygenase1 test
  • Deficiency of steroid 17-alpha-monooxygenase1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Dent disease1 test
  • Dent disease type 11 test
  • Dent disease type 21 test
  • Diabetes insipidus, nephrogenic, autosomal1 test
  • Diabetes insipidus, nephrogenic, X-linked1 test
  • Diabetes insipidus, neurohypophyseal, X-linked1 test
  • Diabetes mellitus, ketosis-prone1 test
  • Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension1 test
  • Diabetes mellitus, transient neonatal, 11 test
  • Diabetes mellitus, transient neonatal, 21 test
  • Diabetes mellitus, transient neonatal, 31 test
  • Disorder of cardiovascular system2 tests
  • Donnai-Barrow syndrome1 test
  • Drash syndrome1 test
  • EAST syndrome1 test
  • EGFR-related lung cancer1 test
  • Ehlers-Danlos syndrome, periodontal type 11 test
  • Ehlers-Danlos syndrome, periodontal type 21 test
  • Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 71 test
  • Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome1 test
  • Epidermolysis bullosa simplex 7, with nephropathy and deafness1 test
  • Episodic ataxia type 11 test
  • Essential fructosuria1 test
  • Exercise-induced hyperinsulinism1 test
  • Fabry disease1 test
  • Factor VII Marburg I Variant Thrombophilia1 test
  • Factor XII deficiency disease1 test
  • Factor XIII, A subunit, deficiency of1 test
  • Factor XIII, b subunit, deficiency of1 test
  • Familial apolipoprotein C-II deficiency1 test
  • Familial chylomicronemia syndrome1 test
  • Familial cold autoinflammatory syndrome 41 test
  • Familial hyperaldosteronism type III1 test
  • Familial hypocalciuric hypercalcemia1 test
  • Familial hypocalciuric hypercalcemia 11 test
  • Familial hypocalciuric hypercalcemia 21 test
  • Familial hypocalciuric hypercalcemia 31 test
  • Familial hypokalemia-hypomagnesemia2 tests
  • Familial hypoparathyroidism2 tests
  • Familial idiopathic steroid-resistant nephrotic syndrome1 test
  • Familial juvenile hyperuricemic nephropathy type 13 tests
  • Familial juvenile hyperuricemic nephropathy type 21 test
  • Familial Mediterranean fever, autosomal dominant1 test
  • Familial partial lipodystrophy, Dunnigan type1 test
  • Familial renal glucosuria1 test
  • Familial steroid-resistant nephrotic syndrome with sensorineural deafness2 tests
  • Familial type 5 hyperlipoproteinemia1 test
  • Familial visceral amyloidosis, Ostertag type1 test
  • Familial X-linked hypophosphatemic vitamin D refractory rickets1 test
  • Fanconi renotubular syndrome 31 test
  • Fanconi-Bickel syndrome1 test
  • Finnish congenital nephrotic syndrome1 test
  • Fish-eye disease1 test
  • Focal segmental glomerulosclerosis 11 test
  • Focal segmental glomerulosclerosis 21 test
  • Focal segmental glomerulosclerosis 31 test
  • Focal segmental glomerulosclerosis 4, susceptibility to1 test
  • Focal segmental glomerulosclerosis 51 test
  • Focal segmental glomerulosclerosis 61 test
  • Foveal hypoplasia 11 test
  • Frasier syndrome1 test
  • Fructose uptake deficiency, SLC2A5 related1 test
  • Fumarase deficiency1 test
  • Gilbert syndrome1 test
  • Glanzmann thrombasthenia1 test
  • Glaucoma 1, open angle, A1 test
  • Glaucoma 1, open angle, F1 test
  • Glaucoma 1, open angle, G1 test
  • Glaucoma 1, open angle, O1 test
  • Glaucoma 3, primary congenital, D1 test
  • Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset1 test
  • Glomerulopathy with fibronectin deposits 21 test
  • Glucocorticoid resistance1 test
  • Glucocorticoid-remediable aldosteronism1 test
  • GNE myopathy2 tests
  • Graves disease1 test
  • Growth delay due to insulin-like growth factor I resistance1 test
  • Growth delay due to insulin-like growth factor type 1 deficiency1 test
  • Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant1 test
  • Hemochromatosis type 11 test
  • Hemochromatosis type 2A1 test
  • Hemochromatosis type 2B1 test
  • Hemochromatosis type 31 test
  • Hemochromatosis type 41 test
  • Hemochromatosis type 51 test
  • Hemolytic uremic syndrome, atypical, susceptibility to, 12 tests
  • Hemorrhage, intracerebral, susceptibility to1 test
  • Hepatic methionine adenosyltransferase deficiency1 test
  • Hereditary angioedema type 11 test
  • Hereditary antithrombin deficiency1 test
  • Hereditary cerebral amyloid angiopathy, Icelandic type1 test
  • Hereditary disease2 tests
  • Hereditary fructosuria1 test
  • Hereditary leiomyomatosis and renal cell cancer1 test
  • Hereditary pancreatitis1 test
  • Hereditary spherocytosis type 41 test
  • Homocystinuria due to methylene tetrahydrofolate reductase deficiency2 tests
  • Hyper-IgM syndrome type 11 test
  • Hyper-IgM syndrome type 21 test
  • Hyper-IgM syndrome type 31 test
  • Hyper-IgM syndrome type 51 test
  • Hyperaldosteronism, familial, type IV1 test
  • Hyperalphalipoproteinemia 11 test
  • Hypercalcemia1 test
  • Hypercalcemia, infantile, 21 test
  • Hypercholesterolemia, autosomal dominant, 31 test
  • Hypercholesterolemia, autosomal dominant, type B1 test
  • Hypercholesterolemia, familial, 11 test
  • Hypercholesterolemia, familial, 41 test
  • Hyperglycinuria1 test
  • Hyperinsulinemic hypoglycemia, familial, 11 test
  • Hyperinsulinemic hypoglycemia, familial, 21 test
  • Hyperinsulinemic hypoglycemia, familial, 41 test
  • Hyperinsulinism due to glucokinase deficiency1 test
  • Hyperinsulinism-hyperammonemia syndrome1 test
  • Hyperlipidemia due to hepatic triglyceride lipase deficiency1 test
  • Hyperlipidemia, familial combined, LPL related1 test
  • Hyperlipoproteinemia, type I1 test
  • Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome1 test
  • Hyperoxaluria1 test
  • Hyperparathyroidism 11 test
  • Hypertriglyceridemia 11 test
  • Hyperuricemic nephropathy, familial juvenile type 41 test
  • Hypoalphalipoproteinemia, primary, 21 test
  • Hypoinsulinemic hypoglycemia and body hemihypertrophy1 test
  • Hypokalemic periodic paralysis, type 11 test
  • Hypoparathyroidism, deafness, renal disease syndrome1 test
  • Hypoparathyroidism, familial isolated, 21 test
  • Hypoparathyroidism-retardation-dysmorphism syndrome1 test
  • Hypophosphatemic nephrolithiasis/osteoporosis 21 test
  • Hypophosphatemic rickets with hyperparathyroidism2 tests
  • Hypophosphatemic rickets, autosomal recessive, 11 test
  • Hypophosphatemic rickets, autosomal recessive, 21 test
  • Hypouricemia, renal, 21 test
  • Idiopathic basal ganglia calcification 11 test
  • Immunoglobulin-mediated membranoproliferative glomerulonephritis1 test
  • Infantile hypophosphatasia1 test
  • Infantile nephronophthisis1 test
  • Infantile-onset periodic fever-panniculitis-dermatosis syndrome1 test
  • Inflammatory bowel disease 11 test
  • Inherited susceptibility to asthma1 test
  • Insulin-resistant diabetes mellitus AND acanthosis nigricans1 test
  • Intellectual disability, autosomal dominant 341 test
  • Intellectual disability, autosomal dominant 481 test
  • Intestinal hypomagnesemia 11 test
  • Irido-corneo-trabecular dysgenesis1 test
  • Isolated growth hormone deficiency type IB1 test
  • Isolated growth hormone deficiency, type 41 test
  • Joubert syndrome 51 test
  • Joubert syndrome with renal defect1 test
  • Juvenile amyotrophic lateral sclerosis with dementia1 test
  • Juvenile nephropathic cystinosis1 test
  • Karyomegalic interstitial nephritis1 test
  • L-ferritin deficiency1 test
  • LAMB2-related infantile-onset nephrotic syndrome1 test
  • Laron-type isolated somatotropin defect1 test
  • Lazy leukocyte syndrome1 test
  • Leber congenital amaurosis 101 test
  • Leprechaunism syndrome1 test
  • Leri-Weill dyschondrosteosis1 test
  • Lesch-Nyhan syndrome1 test
  • Lethal osteosclerotic bone dysplasia1 test
  • Leucine-induced hypoglycemia1 test
  • Liddle syndrome1 test
  • Liddle syndrome 11 test
  • LIPE-related familial partial lipodystrophy1 test
  • Lipoprotein glomerulopathy1 test
  • LIPOPROTEIN(a) QUANTITATIVE TRAIT LOCUS1 test
  • Lowe syndrome1 test
  • Lymphangiomyomatosis1 test
  • Lymphatic malformation 41 test
  • Lysinuric protein intolerance1 test
  • Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss5 tests
  • Maturity onset diabetes mellitus in young1 test
  • Maturity-onset diabetes of the young type 11 test
  • Maturity-onset diabetes of the young type 101 test
  • Maturity-onset diabetes of the young type 111 test
  • Maturity-onset diabetes of the young type 131 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 81 test
  • Maturity-onset diabetes of the young type 92 tests
  • McCune-Albright syndrome1 test
  • McKusick-Kaufman syndrome1 test
  • Meckel syndrome, type 11 test
  • Meckel syndrome, type 61 test
  • Meretoja syndrome1 test
  • Mesangiocapillary glomerulonephritis1 test
  • Mesangiocapillary glomerulonephritis, type II1 test
  • Mevalonic aciduria1 test
  • Microphthalmia with brain and digit anomalies1 test
  • Microvascular complications of diabetes, susceptibility to, 11 test
  • MTHFR THERMOLABILE POLYMORPHISM1 test
  • Multiple endocrine neoplasia, type 11 test
  • Nail-patella syndrome1 test
  • Neonatal alloimmune thrombocytopenia1 test
  • Neonatal diabetes mellitus1 test
  • Nephroblastoma1 test
  • Nephrolithiasis diarrhea syndrome1 test
  • Nephronophthisis 11 test
  • Nephronophthisis 31 test
  • Nephronophthisis 41 test
  • Nephropathic cystinosis1 test
  • Nephrotic syndrome, type 101 test
  • Nephrotic syndrome, type 21 test
  • Nephrotic syndrome, type 31 test
  • Nephrotic syndrome, type 41 test
  • Nephrotic syndrome, type 61 test
  • Nephrotic syndrome, type 81 test
  • Nephrotic syndrome, type 91 test
  • Neurohypophyseal diabetes insipidus1 test
  • Neuropathy, hereditary sensory and autonomic, type 2A1 test
  • Non-acquired combined pituitary hormone deficiency with spine abnormalities1 test
  • Nonpersistence of intestinal lactase1 test
  • Ocular cystinosis1 test
  • Ornithine aminotransferase deficiency1 test
  • Ornithine carbamoyltransferase deficiency1 test
  • Osteoglophonic dysplasia1 test
  • Osteopathia striata with cranial sclerosis1 test
  • Osteopetrosis with renal tubular acidosis1 test
  • Paroxysmal nocturnal hemoglobinuria 12 tests
  • Partial hypoxanthine-guanine phosphoribosyltransferase deficiency2 tests
  • Permanent neonatal diabetes mellitus1 test
  • Pheochromocytoma2 tests
  • Pierson syndrome1 test
  • Pituitary hormone deficiency, combined, 11 test
  • Pituitary hormone deficiency, combined, 21 test
  • PLIN1-related familial partial lipodystrophy1 test
  • Polycystic kidney disease 21 test
  • Polycystic kidney disease 3 with or without polycystic liver disease1 test
  • Polycystic kidney disease 51 test
  • Polycystic kidney disease 6 with or without polycystic liver disease1 test
  • Polycystic kidney disease, adult type1 test
  • Polyglandular autoimmune syndrome, type 11 test
  • Porencephaly 21 test
  • PPARG-related familial partial lipodystrophy1 test
  • Primary hyperoxaluria, type I1 test
  • Primary hyperoxaluria, type II1 test
  • Primary hypomagnesemia2 tests
  • Primary open angle glaucoma1 test
  • Progressive myositis ossificans1 test
  • Progressive osseous heteroplasia1 test
  • Properdin deficiency, X-linked1 test
  • Pseudo von Willebrand disease1 test
  • Pseudohypoaldosteronism type 2B1 test
  • Pseudohypoaldosteronism type 2C1 test
  • Pseudohypoaldosteronism type 2D1 test
  • Pseudohypoaldosteronism type 2E1 test
  • Pseudohypoparathyroidism1 test
  • Pseudohypoparathyroidism type 1B1 test
  • Pyogenic arthritis-pyoderma gangrenosum-acne syndrome1 test
  • Rabson-Mendenhall syndrome1 test
  • Recurrent Neisseria infections due to factor D deficiency1 test
  • Renal cell carcinoma1 test
  • Renal coloboma syndrome1 test
  • Renal cysts and diabetes syndrome2 tests
  • Renal hypodysplasia/aplasia 11 test
  • Renal hypodysplasia/aplasia 21 test
  • Renal hypodysplasia/aplasia 31 test
  • Renal hypomagnesemia 21 test
  • Renal hypomagnesemia 41 test
  • Renal hypomagnesemia 5 with ocular involvement1 test
  • Renal hypomagnesemia 61 test
  • Renal hypoplasia1 test
  • Renal hypoplasia, isolated1 test
  • Renal tubular acidosis with progressive nerve deafness1 test
  • Renal tubular dysgenesis1 test
  • Renal-hepatic-pancreatic dysplasia1 test
  • Renal-hepatic-pancreatic dysplasia 21 test
  • Retinitis pigmentosa 511 test
  • Salla disease2 tests
  • Sarcotubular myopathy2 tests
  • Schimke immuno-osseous dysplasia1 test
  • Senior-Loken syndrome 51 test
  • Senior-Loken syndrome 61 test
  • Sensorineural deafness with mild renal dysfunction1 test
  • Septo-optic dysplasia sequence1 test
  • Short stature due to growth hormone qualitative anomaly1 test
  • Short stature due to partial GHR deficiency1 test
  • Short stature due to primary acid-labile subunit deficiency1 test
  • Short stature-pituitary and cerebellar defects-small sella turcica syndrome1 test
  • Sialic acid storage disease, severe infantile type1 test
  • Sialuria1 test
  • Sitosterolemia1 test
  • Sneddon syndrome1 test
  • Southeast Asian ovalocytosis1 test
  • Tangier disease1 test
  • Thrombomodulin-related bleeding disorder1 test
  • Thrombophilia due to activated protein C resistance1 test
  • Thrombophilia due to protein C deficiency, autosomal dominant1 test
  • Thrombophilia due to protein S deficiency, autosomal dominant1 test
  • Thrombotic thrombocytopenic purpura1 test
  • Thyroid hormone resistance, generalized, autosomal dominant1 test
  • Thyroid hormone resistance, generalized, autosomal recessive1 test
  • Tuberous sclerosis 11 test
  • Tuberous sclerosis 21 test
  • Tumoral calcinosis, hyperphosphatemic, familial, 11 test
  • Type 2 diabetes mellitus1 test
  • Type I complement component 8 deficiency1 test
  • Type II complement component 8 deficiency1 test
  • Vitamin D hydroxylation-deficient rickets, type 1B1 test
  • Vitamin D-dependent rickets, type 11 test
  • Vitamin D-dependent rickets, type 21 test
  • Vitamin K-dependent clotting factors, combined deficiency of, type 11 test
  • Vitamin K-dependent clotting factors, combined deficiency of, type 21 test
  • Warfarin response1 test
  • Williams syndrome1 test
  • Wilms tumor 12 tests
  • Wolfram syndrome1 test
  • Wolfram syndrome 11 test
  • Wolfram syndrome 21 test
  • Wolfram-like syndrome1 test
  • WT1-Related Disorders1 test
  • X-linked agammaglobulinemia2 tests
  • X-linked agammaglobulinemia with growth hormone deficiency1 test
  • X-linked Alport syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Confirmation of research findings
  • Custom Deletion/Duplication Testing
  • Prenatal testing
  • Custom Sequence Analysis
  • Carrier testing
  • Data Storage and Backup
  • Mutation Confirmation
  • Result interpretation

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 99D1063776, Expiration date: 2020-03-19
  • CAP, Number: LAP Number:7186621, Expiration date: 2019-11-15
  • ISO15189, Number: D-ML-13133-01-00, Expiration date: 2028-07-03

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.