Asper Biogene – genetic testing company

with a set of efficient DNA tests

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      • Company profile
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    Asper Metabolic Disorders sample submission form

    Published 01/06/2018

    Asper Metabolic Disorders sample submission form

    Asper Ophthalmics Asper Reprogenetics Asper Oncogenetics Asper Cardiogenetics Asper NeurogeneticsAsper Otogenetics Asper HematologyAsper DysmorphologyAsper EndocrinologyAsper Metabolic DisordersAsper Wellness Asper Paternity

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      • Asper Ophthalmics submission form
      • Asper Reprogenetics submission form
      • Asper Oncogenetics submission form
      • Asper Cardiogenetics submission form
      • Asper Neurogenetics submission form
      • Asper Otogenetics submission form
      • Asper Hematology submission form
      • Asper Dysmorphology submission form
      • Asper Endocrinology submission form
      • Asper Metabolic Disorders submission
      • Asper Wellness submission form
      • Whole Exome Sequencing submission form
      • Whole Genome Sequencing submission form
    • About Us
      • Company profile
      • Management team
      • Contacts
      • Contacts
    • Adjusted gene panels for you
    • Asper Biogene Data Renewal Form
    • Asper Dysmorphology
      • Brain malformations NGS panel
        • List of diseases covered by Brain malformations NGS panel
      • Craniosynostosis NGS panel
        • List of diseases covered by Craniosynostosis NGS panel
      • Microcephaly NGS panel
        • List of diseases covered by Microcephaly NGS panel
      • Noonan Syndrome NGS panel
        • List of diseases covered by Noonan Syndrome NGS panel
      • Skeletal Ciliopathies NGS panel
        • List of diseases covered by Skeletal Ciliopathies NGS panel
      • Skeletal Dysplasia NGS panel
        • List of diseases covered by Skeletal Dysplasia NGS panel
      • Smith-Lemli-Opitz Syndrome
      • Whole Exome Sequencing
    • Asper Endocrinology
      • Androgen Insensitivity Syndrome
      • Combined Pituitary Hormone Deficiency
      • Familial Hypocalciuric Hypercalcemia
      • Hypothyroidism and Thyroid Hormone Resistance NGS panel
      • Maturity Onset Diabetes of the Young (MODY) NGS panel
      • Thyroid Dyshormonogenesis NGS panel
      • Whole Exome Sequencing
    • Asper Hematology
      • Alpha Thalassemia
      • Beta Thalassemia
      • Fanconi Anemia
      • Hereditary Sideroblastic Anemia NGS panel
        • List of diseases covered by Hereditary Sideroblastic Anemia NGS panel
      • Thrombocytopenia NGS panel
      • Whole Exome sequencing
    • Asper Metabolic Disorders
      • Citrullinemia, type 1
      • Fatty Acid Oxidation Disorder NGS panel
        • List of diseases covered by Fatty Acid Oxidation Disorder NGS panel
      • Glutaric Aciduria, type 1
      • Glutaric Aciduria, type 2
      • Glycogen Storage Disease NGS panel
        • List of diseases covered by Glycogen Storage Disease NGS panel
      • Hemochromatosis NGS panel
        • List of diseases covered by Hemochromatosis NGS panel
      • Lysosomal Storage Disease NGS panel
        • List of diseases covered by Lysosomal Storage Disease NGS panel
      • Metabolic Myopathy and Rhabdomyolysis
        • List of diseases covered by Metabolic Myopathy and Rhabdomyolysis NGS panel
      • Methylmalonic Aciduria and Homocystinuria NGS panel
        • List of diseases covered by Methylmalonic Aciduria and Homocystinuria NGS panel
      • Porphyria NGS panel
        • List of diseases covered by Porphyria NGS panel
      • Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency
      • Smith Lemli Opitz Syndrome
      • Urea Cycle Disorder NGS panel
        • List of diseases covered by Urea Cycle Disorder NGS panel
      • Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
      • Whole Exome Sequencing
      • Citrin Deficiency
    • Genetic tests
    • Ordering
      • Ordering information
      • Shipment of samples
      • Supportive services
      • Payment
      • Terms and conditions
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    • NGS service
      • Limitations of the exome sequencing
      • Whole Genome Sequencing
    • News
    • Scientific projects
    • Asper Cardiogenetics
      • Apolipoprotein C-II Deficiency
      • Arrhythmia
        • List of diseases covered by Arrhythmia NGS panel
      • Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy NGS panel
        • List of diseases covered by Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy NGS panel
      • Brugada Syndrome NGS panel
        • List of diseases covered by Brugada Syndrome NGS panel
      • Catecholaminergic Polymorphic Ventricular Tachycardia
        • List of diseases covered by Catecholaminergic Polymorphic Ventricular Tachycardia NGS panel
      • Dilated Cardiomyopathy NGS panel
      • Familial Hypercholesterolemia NGS panel
      • Familial Lipoprotein Lipase Deficiency
      • Familial Thoracic Aortic Aneurysm and Dissection and Related Syndromes NGS panel
      • Hyperlipoproteinemia, type 3
      • Hyperlipoproteinemia, type 5
      • Hypertriglyceridemia NGS panel
      • Hypertrophic Cardiomyopathy NGS panel
      • Lecithin Cholesterol Acyltransferase Deficiency
      • Long QT Syndrome NGS panel
      • Noonan Syndrome NGS panel
      • Pulmonary Arterial Hypertension NGS panel
      • Requirements for Noonan syndrome Prenatal testing
      • Short QT Syndrome NGS panel
      • Statin-Induced Myopathy
      • Tangier Disease
      • Thrombophilia
      • Whole Exome Sequencing
    • Asper Neurogenetics
      • Amyotrophic Lateral Sclerosis NGS panel
        • List of diseases covered by Amyotrophic Lateral Sclerosis NGS panel
      • Autism Spectrum Disorders NGS panel
        • List of diseases covered by Autism Spectrum Disorders NGS panel
      • Charcot-Marie-Tooth Disease
        • List of diseases covered by Charcot-Marie-Tooth Disease NGS panel
      • Congenital Myopathy and Distal Myopathy NGS panel
        • List of diseases covered by Congenital Myopathy and Distal Myopathy NGS panel
      • Cornelia de Lange Syndrome NGS panel
        • List of diseases covered by Cornelia de Lange Syndrome NGS panel
      • Craniosynostosis NGS panel
        • List of diseases covered by Craniosynostosis NGS panel
      • Dystonia NGS panel
        • List of diseases covered by Dystonia NGS panel
      • Epilepsy NGS panel
        • List of diseases covered by Epilepsy NGS panel
      • Fragile X Syndrome
      • Frontotemporal Dementia NGS panel
        • List of diseases covered by Frontotemporal Dementia NGS panel
      • Hereditary Spastic Paraplegia NGS panel
        • List of diseases covered by Hereditary Spastic Paraplegia NGS panel
      • Joubert Syndrome NGS panel
        • List of diseases covered by Joubert Syndrome NGS panel
      • Leukodystrophy and Leukoencephalopathy NGS panel
        • List of diseases covered by Leukodystrophy and Leukoencephalopathy NGS panel
      • Limb-Girdle Muscular Dystrophy NGS panel
        • List of diseases covered by Limb-Girdle Muscular Dystrophy NGS panel
      • Menkes Disease
      • Microcephaly NGS panel
        • List of diseases covered by Microcephaly NGS panel
      • Mitochondrial Diseases
        • List of diseases covered by nuclear genes NGS panel
      • Neurodegeneration with Brain Iron Accumulation NGS panel
        • List of diseases covered by Neurodegeneration with Brain Iron Accumulation NGS panel
      • Parkinson Disease NGS panel
        • List of diseases covered by Parkinson Disease NGS panel
      • Requirements for Prenatal testing
      • Smith-Lemli-Opitz Syndrome
      • Spinocerebellar Ataxia
        • List of diseases covered by Spinocerebellar Ataxia NGS panel
      • Tuberous Sclerosis NGS panel
      • Whole Exome Sequencing
      • Wilson Disease
    • Asper Oncogenetics
      • BRAF gene mutation analysis
        • BRAF gene targeted mutation analysis
      • Breast and Ovarian Cancer
        • List of diseases covered by Breast and Ovarian Cancer NGS panel
      • Cancer Predisposition
        • List of diseases covered by Cancer Predisposition NGS panel
      • Familial Adenomatous Polyposis
      • Fanconi Anemia
        • List of diseases covered by Fanconi Anemia NGS panel
      • Lynch Syndrome/Hereditary Non-Polyposis Colon Cancer – HNPCC
      • Melanoma NGS panel
      • Microsatellite instability testing
        • Microsatellite instability read more
      • MUTYH-associated polyposis genetic testing
      • Nijmegen Breakage Syndrome
      • Polyposis Syndromes
        • List of diseases covered by Polyposis Syndromes NGS panel
      • Thyroid Cancer NGS panel
        • List of diseases covered by Thyroid Cancer NGS panel
      • Whole Exome Sequencing
      • Whole Exome Sequencing
    • Asper Ophthalmics
      • Achromatopsia NGS panel
        • List of diseases covered by Achromatopsia NGS panel
      • Age-Related Macular Degeneration – AMD
        • List of diseases covered by AMD NGS panel
      • Aniridia
      • Anophthalmia/Microphthalmia/Coloboma/Anterior Segment Dysgenesis NGS panel
        • List of diseases covered by Anophthalmia/Microphthalmia/Coloboma/Anterior Segment Dysgenesis
      • Cataract NGS panel
        • List of diseases covered by Cataract NGS panel
      • Choroideremia
      • Eye Diseases NGS panel of 277 genes
        • List of diseases covered by the NGS panel of 277 genes
      • Glaucoma
        • List of diseases covered by Glaucoma NGS panel
      • Norrie Disease
      • Oculocutaneous Albinism, Ocular Albinism, Hermansky-Pudlak Syndrome, Chediak-Higashi Syndrome
        • List of diseases covered by Oculocutaneous Albinism, Ocular Albinism, Hermansky-Pudlak Syndrome, Chediak-Higashi Syndrome NGS panel
      • Papillorenal Syndrome
      • Requirements for Prenatal testing
      • Retinoblastoma
      • Vitreoretinopathy NGS panel
        • List of diseases covered by Vitreoretinopathy NGS panel
      • Whole Exome Sequencing
      • X-Linked Retinoschisis
      • Optic Atrophy
      • Autosomal Dominant Retinitis Pigmentosa
        • List of diseases covered by Autosomal Dominant Retinitis Pigmentosa NGS panel
      • Autosomal Recessive Retinitis Pigmentosa
        • List of diseases covered by Autosomal Recessive Retinitis Pigmentosa NGS panel
      • Bardet Biedl Syndrome, McKusick-Kaufman Syndrome, Borjeson-Forssman-Lehmann Syndrome, Alström Syndrome, Albright Hereditary Osteodystrophy
        • List of diseases covered by Bardet-Biedl Syndrome, McKusick-Kaufman Syndrome, Borjeson-Forssman-Lehmann Syndrome, Alström Syndrome, Albright Hereditary Osteodystrophy NGS panel
      • Cone-Rod Dystrophy
        • List of diseases covered by Cone-Rod Dystrophy NGS panel
      • Congenital Stationary Night Blindness
        • List of diseases covered by Congenital Stationary Night Blindness NGS panel
      • Corneal Dystrophy
        • List of diseases covered by Corneal Dystrophy NGS panel
      • Leber Congenital Amaurosis
        • List of diseases covered by Leber Congenital Amaurosis NGS panel
      • Leber Hereditary Optic Neuropathy
      • Stargardt Disease
      • Usher Syndrome
        • List of diseases covered by Usher Syndrome NGS panel
      • Vitelliform Macular Dystrophy
      • X-Linked Retinitis Pigmentosa
    • Asper Otogenetics
      • Alport Syndrome NGS panel
      • Aminoglycoside-Induced Deafness
      • Branchiootorenal Syndrome NGS panel
      • Jervell and Lange-Nielson Syndrome
      • Pendred Syndrome
      • Proovimaterjal sünnieelseks testimiseks
      • Requirements for Prenatal testing
      • Sensorineural Hearing loss NGS panel
      • Stickler Syndrome NGS panel
      • Treacher Collins Syndrome NGS panel
      • Usher Syndrome NGS panel
      • Waardenburg Syndrome NGS panel
      • Whole Exome Sequencing
      • Zellweger Spectrum Disorders NGS panel
    • Asper Reprogenetics
      • Ashkenazi Jewish diseases
        • List of diseases covered by Ashkenazi Jewish diseases NGS panel
      • Cystic Fibrosis
        • Cystic Fibrosis read more
      • Folate-Dependent Neural Tube Defects
      • Fragile X Syndrome
      • Male Factor Infertility
        • Male Factor Infertility read more
      • Maternal Cell Contamination
      • Requirements for Prenatal testing
      • Requirements for SLOS Prenatal testing
      • Whole Exome Sequencing
      • Carrier Testing NGS panel
    • Asper Wellness
      • Age-Related Macular Degeneration
      • Alzheimer Disease, Recovery from Traumatic Brain Injury, Coronary Heart Disease
      • Athletic performance
        • Athletic performance test – read more
      • Celiac Disease
        • Celiac Disease read more
      • Lactose Intolerance
        • Lactose Intolerance read more
      • Nutri inCode
      • Thrombophilia

    CLIA #99D2046227
    ISO 15189:2012 #M014
    ISO 9001:2015 #EST04518A
    The Health Board license #L01469

    Asper Biogene
    Vaksali 17a, 50410 Tartu, ESTONIA
    Tel +372 7307 295
    Fax +372 7307 298
    E-mail info[at]asperbio.com