Asper Ophthalmics

Achromatopsia
Age-Related Macular Degeneration – AMD
Aniridia
Anophthalmia/Microphthalmia/Coloboma/Anterior Segment Dysgenesis
Autosomal Dominant Optic Atrophy – ADOA
Autosomal Dominant Retinitis Pigmentosa – ADRP
Autosomal Recessive Retinitis Pigmentosa – ARRP
Bardet Biedl Syndrome, McKusick-Kaufman Syndrome, Borjeson-Forssman-Lehmann Syndrome, Alström Syndrome, Albright Hereditary Osteodystrophy
Cataract
Choroideremia
Cone-Rod Dystrophy
Congenital Stationary Night Blindness – CSNB
Corneal Dystrophy
Glaucoma
Leber Congenital Amaurosis – LCA
Leber Hereditary Optic Neuropathy – LHON
Norrie Disease
Oculocutaneous Albinism, Ocular Albinism, Hermansky-Pudlak Syndrome, Chediak-Higashi Syndrome
Papillorenal Syndrome
Retinoblastoma
Stargardt Disease
Usher Syndrome
Vitelliform Macular Dystrophy – VMD
X-Linked Retinitis Pigmentosa – XLRP (RPGR ORF15 included)
X-Linked Retinoschisis
Eye Diseases NGS panel of 277 genes
Exome Sequencing

Asper Reprogenetics

Ashkenazi Jewish Diseases
Carriership Testing
Cystic Fibrosis – CF
Folate-Dependent Neural Tube Defects
Fragile X Syndrome
Male Factor Infertility
Maternal Cell Contamination
Exome Sequencing

Asper Oncogenetics

Breast and Ovarian Cancer
Cancer Predisposition
Familial Adenomatous Polyposis – FAP
Fanconi Anemia
Lynch Syndrome/Hereditary Non-Polyposis Colon Cancer – HNPCC
Melanoma
Microsatellite instability – MSI
MUTYH-associated polyposis – MAP
Nijmegen Breakage Syndrome
Polyposis Syndromes
Thyroid Cancer
Exome Sequencing

Asper Cardiogenetics

Apolipoprotein C-II Deficiency
Arrhythmia
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Brugada Syndrome
Catecholaminergic Polymorphic Ventricular Tachycardia
Dilated Cardiomyopathy
Familial Hypercholesterolemia
Familial Lipoprotein Lipase Deficiency
Familial Thoracic Aortic Aneurysms and Dissections and Related Syndromes
Hyperlipoproteinemia, type 3
Hyperlipoproteinemia, type 5
Hypertriglyceridemia
Hypertrophic Cardiomyopathy
Lecithin Cholesterol Acyltransferase Deficiency
Long QT Syndrome
Noonan Syndrome
Pulmonary Arterial Hypertension
Short QT Syndrome
Statin-Induced Myopathy
Tangier Disease
Venous Thrombosis
Whole Exome Sequencing

Asper Neurogenetics

Amyotrophic Lateral Sclerosis
Autism Spectrum Disorders
Charcot-Marie-Tooth Disease
Cornelia de Lange Syndrome
Craniosynostosis
Dystonia
Fragile X Syndrome
Frontotemporal Dementia
Epilepsy
Hereditary Spastic Paraplegia
Joubert Syndrome
Menkes Disease
Microcephaly
Mitochondrial Diseases
Neurodegeneration with Brain Iron Accumulation
Parkinson Disease
Smith-Lemli-Opitz Syndrome
Spinocerebellar Ataxia
Wilson Disease

Exome Sequencing

Asper Otogenetics

Alport Syndrome
Aminoglycoside-Induced Deafness
Branchiootorenal Syndrome
Jervell and Lange-Nielson Syndrome
Pendred Syndrome
Sensorineural Hearing Loss
Stickler Syndrome
Treacher Collins Syndrome
Usher Syndrome
Waardenburg Syndrome
Zellweger Spectrum Disorders
Exome Sequencing

Asper Hematology

Alpha Thalassemia
Beta Thalassemia
Fanconi Anemia
Thrombocytopenia
Exome Sequencing

Asper Dysmorphology

Brain malformations
Craniosynostosis
Microcephaly
Noonan Syndrome
Skeletal Ciliopathies
Skeletal Dysplasia
Smith-Lemli-Opitz Syndrome
Exome Sequencing

Asper Endocrinology

Androgen Insensitivity Syndrome
Combined Pituitary Hormone Deficiency
Familial Hypocalciuric Hypercalcemia
Hypothyroidism and Thyroid Hormone Resistance
Maturity Onset Diabetes of the Young (MODY)
Thyroid Dyshormonogenesis
Exome Sequencing

Asper Wellness

Age-Related Macular Degeneration
Alzheimer Disease, Recovery from Traumatic Brain Injury, Coronary Heart Disease
Athletic Performance
Celiac Disease
Lactose Intolerance
Nutri inCode
Venous Thrombosis
Exome Sequencing

Asper Paternity

Paternity Testing
Maternity Testing
Siblingship Testing
Grandparentage Testing
Cousin Testing