SLN Cardiogenetics
Apolipoprotein C-II Deficiency
Arrhythmia
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Brugada Syndrome
Catecholaminergic Polymorphic Ventricular Tachycardia
Dilated Cardiomyopathy
Ehlers-Danlos Syndrome
Familial Hypercholesterolemia
Familial Lipoprotein Lipase Deficiency
Familial Thoracic Aortic Aneurysms and Dissections and Related Syndromes UPDATED
Hereditary Hemorrhagic Telangiectasia
Hyperlipoproteinemia, type 3
Hyperlipoproteinemia, type 5
Hypertriglyceridemia
Hypertrophic Cardiomyopathy
Lecithin Cholesterol Acyltransferase Deficiency
Long QT Syndrome
Noonan Spectrum Disorders/Rasopathies
Pulmonary Arterial Hypertension
Short QT Syndrome
Statin-Induced Myopathy
Tangier Disease
Thrombophilia
Whole Exome Sequencing
SLN Dermatology
Cutis Laxa
Ehlers-Danlos Syndrome
Epidermolysis Bullosa
Hermansky-Pudlak Syndrome
Hypotrichosis
Ichthyosis
Melanoma
Neurofibromatosis
Oculocutaneous Albinism
Palmoplantar Keratoderma
Tuberous sclerosis
Waardenburg Syndrome
Whole Exome Sequencing
SLN Dysmorphology
Brain malformations UPDATED
Craniosynostosis
Frazer Syndrome
Microcephaly
Noonan Spectrum Disorders/Rasopathies
Osteogenesis Imperfecta
Skeletal Ciliopathies
Skeletal Dysplasia
Smith-Lemli-Opitz Syndrome
Whole Exome Sequencing
SLN Endocrinology
Androgen Insensitivity Syndrome
Combined Pituitary Hormone Deficiency
Congenital Adrenal Hyperplasia NEW
Familial Hypocalciuric Hypercalcemia
Hypothyroidism and Thyroid Hormone Resistance
Kallmann Syndrome
Maturity Onset Diabetes of the Young (MODY)
Thyroid Dyshormonogenesis
Whole Exome Sequencing
SLN Hematology
Alpha Thalassemia
Beta Thalassemia
Coagulation Disorders
Fanconi Anemia
Hereditary Sideroblastic Anemia
Thrombocytopenia
Whole Exome Sequencing
SLN Metabolic Disorders
Citrin Deficiency
Citrullinemia, type 1
Congenital Disorders of Glycolysation
Fatty Acid Oxidation Disorder
Glutaric Aciduria, type 1
Glutaric Aciduria, type 2
Glycogen Storage Disease
Hemochromatosis
Lysosomal Storage Disease
Metabolic Myopathy and Rhabdomyolysis
Methylmalonic Aciduria and Homocystinuria
Mucopolysaccharidosis NEW
Porphyria
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency
Smith Lemli Opitz Syndrome
Urea Cycle Disorder
Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
Whole Exome Sequencing
SLN Nephrology
Bardet Biedl Syndrome
Bartter Syndrome
Branchiootorenal Syndrome
Ciliopathy
Hemolytic Uremic Syndrome
Hypomagnesemia NEW
Nephronophthisis
Nephrotic Syndrome
Polycystic Kidney Disease
Primary Ciliary Dyskinesia
Senior-Loken Syndrome
Whole Exome Sequencing
SLN Neurogenetics
Amyotrophic Lateral Sclerosis
Autism Spectrum Disorders UPDATED
Brunner Syndrome
Charcot-Marie-Tooth Disease UPDATED
Congenital Myasthenic Syndrome
Congenital Myopathy and Distal Myopathy
Cornelia de Lange Syndrome
Craniosynostosis
Dystonia UPDATED
Familial Hemiplegic Migraine NEW
Fragile X Syndrome
Frontotemporal Dementia
Epilepsy UPDATED
Hereditary Spastic Paraplegia
Joubert Syndrome
Leukodystrophy and Leukoencephalopathy
Limb-Girdle Muscular Dystrophy
Malignant Hyperthermia NEW
Menkes Disease
Microcephaly
Mitochondrial Diseases UPDATED
Neurodegeneration with Brain Iron Accumulation
Parkinson’s Disease
Paroxysmal Dyskinesia NEW
Smith-Lemli-Opitz Syndrome
Spinocerebellar Ataxia UPDATED
Tuberous Sclerosis
Wilson Disease
Whole Exome Sequencing
SLN Oncogenetics
Breast and Ovarian Cancer
Cancer Predisposition
Familial Adenomatous Polyposis
Fanconi Anemia
Lynch Syndrome/Hereditary Non-Polyposis Colon Cancer
Melanoma
Microsatellite instability
MUTYH-associated polyposis
Nijmegen Breakage Syndrome
Polyposis Syndromes
Prostate Cancer
Thyroid Cancer
Von Hippel-Lindau Disease
Whole Exome Sequencing
SLN Ophthalmics
Achromatopsia
Age-Related Macular Degeneration
Aniridia
Anophthalmia/Microphthalmia/Coloboma/Anterior Segment Dysgenesis
Autosomal Dominant Retinitis Pigmentosa
Autosomal Recessive Retinitis Pigmentosa
Bardet Biedl Syndrome, McKusick-Kaufman Syndrome, Borjeson-Forssman-Lehmann Syndrome, Alström Syndrome, Albright Hereditary Osteodystrophy
Cataract
Choroideremia
Cone-Rod Dystrophy
Congenital Fibrosis of Extraocular Muscles NEW
Congenital Stationary Night Blindness
Corneal Dystrophy
Ectopia Lentis
Eye Diseases NGS panel of 288 genes UPDATED
Glaucoma
Leber Congenital Amaurosis
Leber Hereditary Optic Neuropathy
Norrie Disease
Oculocutaneous Albinism, Ocular Albinism, Hermansky-Pudlak Syndrome, Chediak-Higashi Syndrome
Optic Atrophy
Papillorenal Syndrome
Retinoblastoma
Senior-Loken Syndrome
Stargardt Disease
Usher Syndrome
Vitelliform Macular Dystrophy
Vitreoretinopathy
X-Linked Retinitis Pigmentosa (RPGR ORF15 included)
X-Linked Retinoschisis
Whole Exome Sequencing
SLN 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
Whole Exome Sequencing
SLN Reprogenetics
Ashkenazi Jewish Diseases
Carriership Testing
Cystic Fibrosis
Female Infertility UPDATED
Folate-Dependent Neural Tube Defects
Fragile X Syndrome
Male Factor Infertility UPDATED
Maternal Cell Contamination
Primary Ciliary Dyskinesia
Whole Exome Sequencing