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Health in Code S.L.

GTR Lab ID: 320229, Last updated:2016-04-27
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Personnel

Conditions and tests

  • 3-Methylglutaconic aciduria type 21 test
  • Acromicric dysplasia3 tests
  • Adams-Oliver syndrome 52 tests
  • Amyloidogenic transthyretin amyloidosis2 tests
  • Andersen Tawil syndrome1 test
  • Aortic aneurysm, familial thoracic 42 tests
  • Aortic aneurysm, familial thoracic 63 tests
  • Aortic aneurysm, familial thoracic 72 tests
  • Aortic aneurysm, familial thoracic 82 tests
  • Aortic valve disorder2 tests
  • Arrhythmogenic right ventricular cardiomyopathy5 tests
  • Arrhythmogenic right ventricular cardiomyopathy, type 102 tests
  • Arrhythmogenic right ventricular cardiomyopathy, type 112 tests
  • Arrhythmogenic right ventricular cardiomyopathy, type 122 tests
  • Arrhythmogenic right ventricular cardiomyopathy, type 53 tests
  • Arrhythmogenic right ventricular cardiomyopathy, type 82 tests
  • Arrhythmogenic right ventricular cardiomyopathy, type 92 tests
  • Arrhythmogenic right ventricular dysplasia, familial 11 test
  • Arrhythmogenic right ventricular dysplasia, familial, 131 test
  • Arrhythmogenic right ventricular dysplasia, familial, 22 tests
  • Arterial tortuosity syndrome2 tests
  • Atrial fibrillation1 test
  • Atrial fibrillation, familial, 11 test
  • Atrial fibrillation, familial, 102 tests
  • Atrial fibrillation, familial, 131 test
  • Atrial fibrillation, familial, 31 test
  • Atrial fibrillation, familial, 41 test
  • Atrial fibrillation, familial, 91 test
  • Atrial septal defect 51 test
  • Atrial septal defect 7 with or without atrioventricular conduction defects2 tests
  • Atrioventricular septal defect 21 test
  • Autosomal recessive cutis laxa type 1B1 test
  • Becker muscular dystrophy1 test
  • Benign scapuloperoneal muscular dystrophy with cardiomyopathy2 tests
  • Brugada syndrome2 tests
  • Brugada syndrome 13 tests
  • Brugada syndrome 51 test
  • Cardiac arrhythmia5 tests
  • Cardiac valvular dysplasia, X-linked2 tests
  • Cardiofaciocutaneous syndrome 12 tests
  • Cardiofaciocutaneous syndrome 23 tests
  • Cardiofaciocutaneous syndrome 32 tests
  • Cardiofaciocutaneous syndrome 42 tests
  • Cardiomyopathy1 test
  • Cardiomyopathy dilated with woolly hair and keratoderma2 tests
  • Cardiomyopathy, dilated, 1NN1 test
  • Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis2 tests
  • Carpal tunnel syndrome1 test
  • Catecholaminergic polymorphic ventricular tachycardia1 test
  • Charcot-Marie-Tooth disease type 2B12 tests
  • Chylomicron retention disease1 test
  • Conduction disorder of the heart2 tests
  • Congenital aneurysm of ascending aorta1 test
  • Congenital contractural arachnodactyly2 tests
  • Congenital generalized lipodystrophy type 11 test
  • Congenital generalized lipodystrophy type 21 test
  • Congenital heart disease2 tests
  • Congenital muscular dystrophy, LMNA-related2 tests
  • Conotruncal heart malformations2 tests
  • Costello syndrome4 tests
  • Creatine phosphokinase, elevated serum1 test
  • Cutis laxa, autosomal dominant 12 tests
  • Dilated cardiomyopathy 1A2 tests
  • Dilated cardiomyopathy 1BB2 tests
  • Dilated cardiomyopathy 1C2 tests
  • Dilated cardiomyopathy 1E2 tests
  • Dilated cardiomyopathy 1FF1 test
  • Dilated cardiomyopathy 1G1 test
  • Dilated cardiomyopathy 1I2 tests
  • Dilated cardiomyopathy 1P2 tests
  • Dilated cardiomyopathy 1R1 test
  • Dilated cardiomyopathy 1S1 test
  • Dilated cardiomyopathy 1Y1 test
  • Dilated cardiomyopathy 1Z1 test
  • Dilated cardiomyopathy 2A1 test
  • Dilated cardiomyopathy 3B1 test
  • Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome2 tests
  • Distal myopathy Markesbery-Griggs type1 test
  • Distal myopathy, Tateyama type1 test
  • Doyne honeycomb retinal dystrophy1 test
  • Duchenne muscular dystrophy1 test
  • Dystransthyretinemic euthyroidal hyperthyroxinemia1 test
  • Early repolarization associated with ventricular fibrillation1 test
  • Ectopia lentis et pupillae2 tests
  • Ectopia lentis, isolated autosomal recessive2 tests
  • Ectopia lentis, isolated, autosomal dominant3 tests
  • Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form2 tests
  • Ehlers-Danlos syndrome, classic type2 tests
  • Ehlers-Danlos syndrome, hydroxylysine-deficient2 tests
  • Ehlers-Danlos syndrome, procollagen proteinase deficient2 tests
  • Ehlers-Danlos syndrome, type 32 tests
  • Ehlers-Danlos syndrome, type 42 tests
  • Emery-Dreifuss muscular dystrophy 7, autosomal dominant2 tests
  • Epidermal nevus1 test
  • Epidermal nevus syndrome4 tests
  • Epidermolysis bullosa, lethal acantholytic2 tests
  • Fabry disease2 tests
  • Familial hypercholesterolemia5 tests
  • Familial hypertriglyceridemia1 test
  • Familial hypertrophic cardiomyopathy 14 tests
  • Familial hypertrophic cardiomyopathy 101 test
  • Familial hypertrophic cardiomyopathy 111 test
  • Familial hypertrophic cardiomyopathy 131 test
  • Familial hypertrophic cardiomyopathy 182 tests
  • Familial hypertrophic cardiomyopathy 21 test
  • Familial hypertrophic cardiomyopathy 31 test
  • Familial hypertrophic cardiomyopathy 41 test
  • Familial hypertrophic cardiomyopathy 61 test
  • Familial hypertrophic cardiomyopathy 71 test
  • Familial hypertrophic cardiomyopathy 81 test
  • Familial hypertrophic cardiomyopathy 91 test
  • Familial hypobetalipoproteinemia1 test
  • Familial partial lipodystrophy1 test
  • Familial partial lipodystrophy 23 tests
  • Familial partial lipodystrophy 31 test
  • Familial partial lipodystrophy 41 test
  • Familial partial lipodystrophy 51 test
  • Familial restrictive cardiomyopathy4 tests
  • Familial restrictive cardiomyopathy 11 test
  • Familial restrictive cardiomyopathy 31 test
  • FG syndrome1 test
  • FG syndrome 22 tests
  • Fish-eye disease1 test
  • Frontometaphyseal dysplasia2 tests
  • Geleophysic dysplasia 23 tests
  • Generalized epilepsy with febrile seizures plus, type 11 test
  • Geroderma osteodysplastica1 test
  • Giant pigmented hairy nevus1 test
  • Gingival fibromatosis 12 tests
  • Glycogen storage disease of heart, lethal congenital1 test
  • Glycogen storage disease, type II3 tests
  • Heart-hand syndrome, Slovenian type2 tests
  • Hereditary myopathy with early respiratory failure1 test
  • Homocystinuria due to CBS deficiency2 tests
  • Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type1 test
  • Hutchinson-Gilford syndrome2 tests
  • Hypoplastic left heart syndrome 22 tests
  • Hypothyroidism, congenital, nongoitrous, 52 tests
  • Insulin-resistant diabetes mellitus1 test
  • Intestinal pseudoobstruction neuronal chronic idiopathic X-linked2 tests
  • Jervell and Lange-Nielsen syndrome 11 test
  • Jervell and Lange-Nielsen syndrome 21 test
  • Juvenile myelomonocytic leukemia2 tests
  • Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome2 tests
  • Keratosis palmoplantaris striata II2 tests
  • Left ventricular noncompaction5 tests
  • Left ventricular noncompaction 11 test
  • Left ventricular noncompaction 101 test
  • Left ventricular noncompaction 61 test
  • Legius syndrome1 test
  • LEOPARD syndrome 14 tests
  • LEOPARD syndrome 21 test
  • LEOPARD syndrome 32 tests
  • Lethal tight skin contracture syndrome3 tests
  • Limb-girdle muscular dystrophy, type 1B2 tests
  • Limb-girdle muscular dystrophy, type 1C1 test
  • Limb-girdle muscular dystrophy, type 2J1 test
  • Lipodystrophy, congenital generalized, type 31 test
  • Lipodystrophy, congenital generalized, type 41 test
  • Loeys-Dietz syndrome1 test
  • Loeys-Dietz syndrome 13 tests
  • Loeys-Dietz syndrome 23 tests
  • Loeys-Dietz syndrome 32 tests
  • Loeys-Dietz syndrome 42 tests
  • Loeys-Dietz syndrome 53 tests
  • Long QT syndrome8 tests
  • Long QT syndrome 11 test
  • Long QT syndrome 101 test
  • Long QT syndrome 21 test
  • Long QT syndrome 32 tests
  • Long QT syndrome 51 test
  • Long QT syndrome 61 test
  • Long QT syndrome 91 test
  • Macular degeneration, early-onset2 tests
  • Mandibuloacral dysostosis2 tests
  • Mandibuloacral dysplasia with type B lipodystrophy1 test
  • Marfan syndrome3 tests
  • MASS syndrome3 tests
  • Maturity-onset diabetes of the young, type 21 test
  • Melnick-Needles syndrome2 tests
  • Mental retardation, X-linked, syndromic, Raymond type1 test
  • Metachondromatosis2 tests
  • Moyamoya disease 53 tests
  • Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects1 test
  • Multisystemic smooth muscle dysfunction syndrome3 tests
  • Muscular dystrophy, limb-girdle, type 2r2 tests
  • Myhre syndrome2 tests
  • Myofibrillar myopathy 12 tests
  • Myofibrillar myopathy, filamin C-related1 test
  • Myofibrillar myopathy, ZASP-related2 tests
  • Myopathy2 tests
  • Myopathy, distal, 11 test
  • Myopathy, distal, 41 test
  • Myopathy, early-onset, with fatal cardiomyopathy1 test
  • Myosin storage myopathy1 test
  • Naxos disease2 tests
  • Neurocutaneous melanosis1 test
  • Noonan syndrome 14 tests
  • Noonan syndrome 33 tests
  • Noonan syndrome 42 tests
  • Noonan syndrome 51 test
  • Noonan syndrome 61 test
  • Noonan syndrome 72 tests
  • Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia1 test
  • Noonan-like syndrome with loose anagen hair1 test
  • Ohdo syndrome, X-linked1 test
  • Osler hemorrhagic telangiectasia syndrome2 tests
  • Osteogenesis imperfecta type I2 tests
  • Osteogenesis imperfecta type III2 tests
  • Osteogenesis imperfecta with normal sclerae, dominant form2 tests
  • Osteogenesis imperfecta, recessive perinatal lethal2 tests
  • Oto-palato-digital syndrome, type I2 tests
  • Oto-palato-digital syndrome, type II2 tests
  • Paroxysmal familial ventricular fibrillation 12 tests
  • Periventricular nodular heterotopia 12 tests
  • Primary dilated cardiomyopathy17 tests
  • Primary familial hypertrophic cardiomyopathy8 tests
  • Primary pulmonary hypertension4 tests
  • Progressive familial heart block type 1A2 tests
  • Pulmonary veno-occlusive disease1 test
  • Rasopathy1 test
  • Rippling muscle disease1 test
  • Scapuloperoneal myopathy, MYH7-related1 test
  • Scapuloperoneal syndrome, neurogenic, Kaeser type2 tests
  • short QT syndrome2 tests
  • Short QT syndrome 11 test
  • Short QT syndrome 21 test
  • Short QT syndrome 31 test
  • Shprintzen-Goldberg syndrome2 tests
  • Sick sinus syndrome 1, autosomal recessive2 tests
  • Skin fragility woolly hair syndrome2 tests
  • Stiff skin syndrome1 test
  • Sudden cardiac death3 tests
  • SUDDEN INFANT DEATH SYNDROME2 tests
  • Supravalvar aortic stenosis2 tests
  • Tangier disease1 test
  • Terminal osseous dysplasia2 tests
  • Tetralogy of Fallot2 tests
  • Timothy syndrome1 test
  • Ventricular septal defect 32 tests
  • Ventricular tachycardia, catecholaminergic polymorphic, 13 tests
  • Ventricular tachycardia, catecholaminergic polymorphic, 22 tests
  • Weill-Marchesani syndrome 23 tests
  • Wolff-Parkinson-White pattern1 test
  • Wrinkly skin syndrome1 test
  • X-linked mental retardation with marfanoid habitus syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Confirmation of research findings
  • Data Storage and Backup
  • Mutation Confirmation
  • Result interpretation
  • Targeted exome sequencing of inherited cardiomyopathies

List of certifications/licenses

Certifications

  • EMQN, Number: DNA-Seq Full, Expiration date: 2017-01-05
  • EMQN, Number: NextGen DNA Sequencing, Expiration date: 2017-01-26
  • UNE-EN ISO 14001, Number: ES064285-1, Expiration date: 2018-05-13
  • UNE-EN ISO 9001, Number: ES0645001, Expiration date: 2018-05-13

Licenses

  • State License, Number: C-15-002226, Expiration date: 2020-01-14

Participation in external programs

Standardization programs

  • Other

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