Gene Panel

Dante Genomics Gene Panels offer a profound understanding of your genetic makeup, providing detailed insights into your health and the potential risk factors for various conditions. These gene panels are expertly designed to cater to your specific interests and health objectives, ensuring a highly personalized genetic testing experience. Backed by cutting-edge technology, our reports decode the complexities of your DNA, empowering you with life-changing information.
Cardiovascular

Main syndromes and disorders covered

Read More
Haematology

Main syndromes and disorders covered

Read More
Oncology

Main syndromes and disorders covered

Read More
Nephrology

Main syndromes and disorders covered

Read More
Endocrinology

Main syndromes and disorders covered

Read More
Gastroenterology

Main syndromes and disorders covered

Read More
Fertility

Main syndromes and disorders covered

Read More
Pulmonology

Main syndromes and disorders covered

Read More
Immunology

Main syndromes and disorders covered

Read More
Metabolic disorders

Main syndromes and disorders covered

Read More
Malformations and skeletal-connective tissue disorders

Main syndromes and disorders covered

Read More
Othorinolaringoiatry

Main syndromes and disorders covered

Read More
Neurology

Main syndromes and disorders covered

Read More
Ophthalmology

Main syndromes and disorders covered

Read More
Dante Labs Italy (Head Office)

Dante Labs SRL Tecnopolo d’Abruzzo, SS17 67100 L’Aquila (AQ) Italy

  • information@dantelabs.com
Dante Labs Dubai

Digital Park, Dubai Silicon Oasis, Building B3 P.O. BOX 341281, Dubai United Arab Emirates

  • information@dantelabs.com
Dante Health Care (PVT) Ltd.

Ground Floor, Plot no. 44-W, Aalay Plaza, Fazal-e-Haq Road, Blue Area, Islamabad, Pakistan

  • info@dantelabs.pk
  • +92 (51) 877 4370
  • +92 (317) 877 4370
Facebook Linkedin Instagram Youtube

Copyright Dante Health Care PVT ltd 2023 All Rights Reserved

Syndromes & Disorders Covered

  • Arrhythmogenic right ventricular cardiomyopathy
  • Brugada syndrome
  • Catecholaminergic polymorphic ventricular tachycardia
  • Congenital heart defects
  • Dilated cardiomyopathy
  • Dolichoectasia
  • Hereditary arrhythmia syndromes
  • Hereditary hemorrhagic telangiectasia
  • Hypomagnesemia
  • Long QT syndrome
  • Short QT syndrome
  • Familial Timothy syndrome
  • Hypertriglyceridemia

Syndromes & Disorders Covered

  • Afibrinogenemia
  • Arthrogryposis-renal dysfunction-cholestasis syndrome
  • Coagulation factor disorders
  • Hemophilia
  • Hereditary angioedema
  • Hereditary hemorrhagic telangiectasia
  • Hermasky-Pudlak syndrome
  • Platelet related disorders
  • Shwachman-Diamond syndrome
  • Thrombocytopenia
  • Thrombophilia
  • Bleeding disorders
  • Bone marrow failure syndrome
  • Congenital dyserythropoietic anemia
  • Congenital sideroblastic anemia
  • Diamond-Blackfan anemia
  • Fanconi anemia
  • Hemolvtic anemias
  • Hemophagocytic lymphohistiocytosis
  • Hereditary spherocytosis
  • Megaloblastic anemia
  • Seckel syndrome
  • Sitosterolemia

Syndromes & Disorders Covered

  • Breast cancer
  • Beckwith-Wiedemann syndrome
  • Endometrial cancer
  • Familial adenomatous polyposis
  • Gastric cancer
  • Gastrointestinal stromal tumor
  • Hereditary Paraganglioma/ Pheochromocytoma
  • Melanoma
  • Ovarian cancer
  • Pancreatic cancer
  • Paragangliomas/Pheochromocytoma/
  • Gastrointestinal stromal
  • Prostate cancer
  • Renal cancer
  • Retinoblastoma
  • Rothmund-Thomson syndrome (Type 2)
  • Skin cancer
  • Thyroid cancer
  • Uterine cancer
  • Leukemia
  • Malignant brain tumors
  • Lymphomas
  • Bone cancer
  • Neuroblastoma
  • Wilms tumor
  • Wilms tumor
  • Rhabdomyosarcoma

Syndromes & Disorders Covered

  • Alport syndrome
  • Bardet-Biedl syndrome
  • Barter syndrome
  • Combined pituitary hormone deficiency
  • Focal segmental glomerulosclerosis
  • Heterotaxy syndrome
  • Hypogonadotropic hypogonadism
  • Intrahepatic cholestasis
  • Joubert syndrome
  • Kallmann syndrome
  • Leber congenital amaurosis
  • Meckel syndrome
  • Nephronophthisis
  • Nephrotic syndrome
  • Neonatal mitochondrial hepatopathies
  • Polycystic kidney disease
  • Pseudohypoaldosteronism
  • Primary ciliary dyskinesia
  • Renal tubular acidosis
  • Renal tubular dysgenesis
  • Skeletal dysplasia
  • Skeletal ciliopathy

Syndromes & Disorders Covered

  • Bardet-Biedl syndrome
  • Congenital glycosylation disease
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Diabetes insipidus
  • Growth hormone deficiency
  • Familial hypercholesterolemia
  • Hypoglycemia
  • Maturity onset diabetes of the young
  • Neonatal diabetes
  • Obesity
  • Pancreatic cancer
  • Pancreatitis
  • Congenital adrenal hyperplasia

Syndromes & Disorders Covered

  • Intrahe patic cholestasis of pregnancy
  • Dubin-Johnson Syndrome
  • Inflammatory skin and bowel disease
  • Congenital bile acid synthesis defect
  • Hyperlipoproteinemia
  • Hypertriglyceridemia
  • Familial hypercholane mia
  • Hereditary chronic pancreatitis
  • Congenital short bowel syndrome
  • Sclerosing cholangitis, neonatal
  • Congenital chronic diarrhea with protein-losing enteropathy
  • Hirschsprung disease
  • Waardenburg-Shah syndrome
  • Congenital tufting enteropathy
  • Colorectal adenocarcinoma
  • Colon adenocarcinoma
  • Digestive System Carcinoma
  • Duodenal Adenocarcinoma
  • Esophageal adenocarcinoma

Syndromes & Disorders Covered

  • Complete androgen insensitivity syndrome
  • Hypogonadotropic hypogonadism
  • Monogenic causes of female infertility
  • Ovarian hyperstimulation syndrome
  • Premature ovarian failure
  • Turner syndrome
  • CFTR-associated infertility
  • Hypogonadotropic hypogonadism
  • Klinefelter syndrome
  • Monogenic causes of male infertility
  • Primary ciliary dyskinesia
  • Spermatogenic failure
  • Y chromosome microdeletions

Syndromes & Disorders Covered

  • Central hypoventilation syndrome
  • Comprehensive pulmonary disease
  • Surfactant metabolism dysfunction
  • Idiopathic pulmonary fibrosis
  • Neonatal acute respiratory distress syndrome
  • Hereditary pulmonary arterial hypertension
  • Pulmonary veno-occlusive disease
  • Primary ciliary dyskinesia
  • Cystic fibrosis
  • Idiopathic bronchiectasis
  • Hereditary pulmonary alveolar proteinosis

Syndromes & Disorders Covered

  • Bleeding disorders
  • Bone marrow failure syndrome
  • Congenital dyserythropoietic anemia
  • Congenital sideroblastic anemia
  • Diamond-Blackfan anemia
  • Fanconi anemia
  • Hemolvtic anemias
  • Hemophagocytic lymphohistiocytosis
  • Hereditary spheroctosis
  • Megaloblastic anemia
  • Seckel syndrome
  • Sito ste rolemia
  • Thrombocvtopenia
  • Anhidrotic ectodermal dysplasia with immunodeficiency
  • Autoinflammatory disorders
  • Common variable immunodeficiency
  • Complement deficiencies (atypical hemolytic uremic (syndrome)
  • Congenital defects of phagocyte (Neutropenia, Shwachman-Diamond Syndrome, functional defects)
  • Defects of intrinsic and innate immunity (predisposition (to viral, bacterial, fungal and parasitic infections)
  • Defects of Vitamin B12 and folate metabolism
  • Diseases of immune dysregulation (Hemophagocytic (lymphohistioctosis. EBV susceptibility)
  • DNA repair defects
  • Hyper IgE syndromes
  • Immunodeficiencies affecting cellular and humoral immunity (Severe combined immunodeficiencies; Combined immunodeficiencies)
  • Immuno-osseous dysplasias
  • Mendelian susceptibility to mycobacterial disease
  • Predominantly antibody deficiencies (hypogammaglobulinemia, other antibody deficiencies)
  • Syndromes with autoimmunity

Syndromes & Disorders Covered

  • Aicardi-Goutieres syndrome
  • Autoimmune lymphoproliferative syndrome
  • Ceroid lipofuscinosis
  • Ceroid lipofuscinosis
  • Familial hypercholesterolemia
  • Fatty acid oxidation disorder
  • Fatty liver disease
  • Glycogen storage disease
  • Hemophagocytic lymphoistiocytosis
  • Hereditary hemochromatosis
  • Hereditary hemochromatosis
  • Leigh Syndrome & Mitochondrial Encephalopathy
  • Leukodystrophy and peroxisome biogenesis disorders
  • Lipodystrophy syndromes
  • Lysosomal storage disease
  • Maple syrup urine disease
  • Methylmalonic acidemia
  • Mucopolysaccharidosis
  • Neurodegeneration with Brain Iron Accumulation
  • Non-ketotic hyperglycinemia
  • Organic acidemias
  • Porphyria
  • Refsum disease
  • Urea cycle disorder

Syndromes & Disorders Covered

  • Abnormal mineralization
  • High bone density disorders
  • Osteogenesis imperfecta
  • Osteopetrosis
  • Low bone density disorders
  • Bardet-Biedl syndrome
  • Bardet-Biedl syndrome
  • Cardiofaciocutaneous syndrome
  • Cerebral cavernous malformations
  • Ciliopathies
  • Cleft lip and palate
  • Coffin-Siris syndrome
  • Cornelia de Lange syndrome
  • Ciliopathic skeletal dysplasias
  • Craniosynostosis and craniofacial disorders
  • Heterotaxy syndrome
  • Hirschsprung disease
  • Holoprosencephaly
  • Klippel-Feil syndrome
  • Lissencephaly and brain malformation
  • Meckel syndrome
  • Metaphyseal dysplasia
  • Micro syndrome
  • Microphthalmia/anophthalmia/coloboma spectrum
  • Multiple epiphyseal dysplasia
  • Neurofibromatosis
  • Noonan-RASopathies syndromes
  • Seckel syndrome
  • Skeletal dvsplasia extended
  • Stickler syndrome
  • Tuberous sclerosis
  • Waardenburg syndrome

Syndromes & Disorders Covered

  • Alport syndrome
  • Coffin-Lowry snydrome
  • Deafness autosomal recessive and dominant
  • Non-syndromic hearing loss
  • Pendred syndrome
  • Perrault syndrome
  • Pfeiffer syndrome
  • Sensorineural hearing loss
  • Stickler syndrome
  • Syndromic hearing loss
  • Usher syndrome
  • Waardenburg syndrome
  • Wolfram syndrome

Syndromes & Disorders Covered

  • Ataxia (1151 Genes)
  • Amyotrophic Lateral Sclerosis (636 Genes)
  • Arthrogryposis Multiplex Congenita (151 Genes)
  • Autism (662 Genes)
  • Dementia (526 Genes)
  • Dystonia (559 Genes)
  • Epileptic Encephalopathy (301 Genes)
  • Familial Hemiplegic Migraine (S Genes)
  • Frontotemporal Dementia (50 Genes)
  • Joubert syndrome (363 Genes)
  • Leigh Syndrome (254 Genes)
  • Leukodystrophy (156 Genes)
  • Meckel Gruber Syndrome (194 Genes)
  • Muscular Dystrophy (462 Genes)
  • Parkinson (436 Genes)
  • Spastic Paraplegia (248 Genes)
  • Tuberous sclerosis (103 Gene)

Syndromes & Disorders Covered

  • Achromatopsia (ACHM) Panel
  • Albinism Oculocutaneous Albinism (OCA) Panel
  • Alport Syndrome Panel
  • Microphthalmia/Anophthalmia/ Coloboma Panel
  • Axenfeld-Rieger Syndrome Panel
  • Comprehensive Cataracts Panel
  • Comprehensive Ocular Disorders Panel
  • Corneal Dystrophies Panel
  • Flecked retina
  • Glaucoma Panel
  • Hermansky-Pudlak Syndrome (HPS) Panel
  • Stickler Syndrome Panel
  • Strabismus Syndrome or Congenital Fibrosis of Extraocular Muscles (Ocular Motility Disorder) Panel
  • Usher Syndrome Panel
  • Comprehensive Vitreoretinopathy Panel
  • Warburg Micro Syndrome Panel
  • Hypopigmentation Panel
  • Leber Congenital Amaurosis Panel
  • Leber Congenital Amaurosis Panel
  • Stargardt Disease (STGD) and Macular Dystrophies Panel
  • Early-Onset High Myopia Panel
  • Congenital Stationary Night Blindness Panel
  • Chronic Progressive External Ophthalmoplegia (СРЕО/РЕО) Panel
  • Optic Atrophy Panel
  • Autosomal Dominant Retinitis Pigmentosa (RP) Panel
  • Autosomal Recessive Retinitis Pigmentosa (RP) Panel
  • Autosomal Recessive Retinitis Pigmentosa (RP) Panel
  • Septo-optic Dysplasia Spectrum Panel
  • Xeroderma Pigmentosum (XP) Panel
  • Wolfram Syndrome Panel
Facebook Linkedin Youtube