Bullous Skin Disease,Colorectal Cancer,Gastric Cancer,Skin Disease,Nephrotic Syndrome, Type 3,Lissencephaly,Wolf-Hirschhorn Syndrome,Leigh Syndrome

Breast Giant Fibroadenoma

Disease Of Mental Health,Leukoencephalopathy With Vanishing White Matter,Non-Syndromic X-Linked Intellectual Disability,Deafness, Autosomal Recessive 104,Syndromic X-Linked Intellectual Disability

Type 1 Diabetes Mellitus 20,Epilepsy, Rolandic, With Paroxysmal Exercise-Induced Dystonia And Writer'S Cramp,Migraine With Or Without Aura 1,Malignant Migrating Partial Seizures Of Infancy,Ohtahara Syndrome,Seizure Disorder,Childhood Absence Epilepsy,Epilepsy,Erythromelalgia,Splenic Sequestration,Episodic Ataxia,Hereditary Episodic Ataxia,Focal Epilepsy,Developmental And Epileptic Encephalopathy 14,Movement Disease,Epilepsy With Generalized Tonic-Clonic Seizures,Familial Febrile Seizures,Central Nervous System Origin Vertigo,Landau-Kleffner Syndrome,Reflex Epilepsy,Low-Grade Astrocytoma,Scn2a Related Disorders,Hemoglobin D Disease,Hemoglobin E Disease,Hemoglobin C Disease,Hemoglobinopathy,Scrapie,Familial Periodic Paralysis,Trigeminal Nerve Disease,Paroxysmal Extreme Pain Disorder,Paramyotonia Congenita Of Von Eulenburg,Febrile Seizures, Familial, 5,Early Myoclonic Encephalopathy,Non-Specific Syndromic Intellectual Disability,Febrile Seizures, Familial, 2,Congenital Hemolytic Anemia,Genetic Epilepsy With Febrile Seizures Plus,Hypokalemic Periodic Paralysis, Type 1,Hyperkalemic Periodic Paralysis,Encephalopathy,Febrile Seizures,Benign Neonatal Seizures,Migraine, Familial Hemiplegic, 3,Alacrima, Achalasia, And Mental Retardation Syndrome,Partial Motor Epilepsy,Benign Epilepsy With Centrotemporal Spikes,Benign Familial Neonatal Epilepsy,West Syndrome,Disease Of Mental Health,Febrile Seizures, Familial, 1,Chronic Wasting Disease,Developmental And Epileptic Encephalopathy 11,Alpha-Thalassemia,Hemoglobin H Disease,Brugada Syndrome,Lennox-Gastaut Syndrome,Coffin-Siris Syndrome 1,Neonatal Period Electroclinical Syndrome,Infancy Electroclinical Syndrome,Childhood Electroclinical Syndrome,Adolescence-Adult Electroclinical Syndrome,Early Onset Absence Epilepsy,Early Infantile Epileptic Encephalopathy,Kuru,Developmental And Epileptic Encephalopathy 13,Coffin-Siris Syndrome 4,Pervasive Developmental Disorder,Autism Spectrum Disorder,Dravet Syndrome,Benign Familial Infantile Epilepsy,Generalized Epilepsy With Febrile Seizures Plus,Episodic Ataxia, Type 9,Seizures, Benign Familial Infantile, 3,Photosensitive Epilepsy,Autosomal Dominant Non-Syndromic Intellectual Disability,Epilepsy, Myoclonic Juvenile,Autism,Autosomal Dominant Nocturnal Frontal Lobe Epilepsy,Epilepsy, Idiopathic Generalized

Immunodeficiency 14,Non-Syndromic X-Linked Intellectual Disability

Prune Belly Syndrome,Cerebellar Hypoplasia,Ventricular Septal Defect,Bone Disease,Mitral Valve Disease,Heart Disease,Physical Disorder,Intestinal Pseudo-Obstruction,Seizure Disorder,Epilepsy,Myofibrillar Myopathy,Melanoma,Connective Tissue Disease,Exophthalmos,Dyslexia,Myalgic Encephalomyelitis/Chronic Fatigue Syndrome,X-Linked Chronic Idiopathic Intestinal Pseudo-Obstruction,Hyperostosis,Constipation,Oto-Palatal-Digital Syndrome,Nodular Neuronal Heterotopia,Congenital Nervous System Abnormality,X-Linked Keloid Scarring-Reduced Joint Mobility-Increased Optic Cup-To-Disc Ratio Syndrome,Otopalatodigital Syndrome Spectrum Disorder,Frontometaphyseal Dysplasia,High-Grade Astrocytoma,Intestinal Obstruction,Flna-Related Periventricular Nodular Heterotopia,Migraine With Aura,Infantile Digital Fibromatosis,Aortic Valve Disease 1,Syphilitic Encephalitis,X-Linked Ehlers-Danlos Syndrome,Spondylocarpotarsal Synostosis Syndrome,Lung Disease,Skeletal Dysplasias,Blood Group, I System,Boomerang Dysplasia,Congenital Short Bowel Syndrome,Ehlers-Danlos Syndrome,X-Linked Otopalatodigital Spectrum Disorders,Tricuspid Valve Prolapse,Short Bowel Syndrome,Aortic Valve Insufficiency,Ebstein Anomaly,Anteroseptal Myocardial Infarction,Microcephaly,Aneurysm,Hydrocephalus,Tracheal Disease,Tracheal Stenosis,Myopathy, Myofibrillar, 5,Alacrima, Achalasia, And Mental Retardation Syndrome,Hydronephrosis,Cleft Palate, Isolated,Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked,Periventricular Nodular Heterotopia 1,West Syndrome,Disease Of Mental Health,Terminal Osseous Dysplasia,Lubs X-Linked Mental Retardation Syndrome,Bernard-Soulier Syndrome,Fg Syndrome 2,Aortic Aneurysm,Hypothalamic Neoplasm,Thrombocytopenia,Diencephalic Neoplasm,Orthostatic Intolerance,Periventricular Nodular Heterotopia,Loeys-Dietz Syndrome,Odontochondrodysplasia,Bleeding Disorder, Platelet-Type, 19,Atelosteogenesis,Intestinal Pseudoobstruction With Patent Ductus Arteriosus And Natal Teeth,Abruzzo-Erickson Syndrome,Miller-Dieker Lissencephaly Syndrome,Fibroma,Aicardi Syndrome,Otopalatodigital Syndrome, Type Ii,Aortic Aneurysm, Familial Thoracic 1,Aortic Aneurysm, Familial Thoracic 2,Opitz-Kaveggia Syndrome,Focal Dermal Hypoplasia,Frontometaphyseal Dysplasia 1,Patent Ductus Arteriosus 1,Keloid Formation,Melnick-Needles Syndrome,Larsen Syndrome,Scoliosis,Otopalatodigital Syndrome, Type I,Omphalocele,Arterial Tortuosity Syndrome,Marfan Syndrome,Cardiac Valvular Dysplasia, X-Linked,Band Heterotopia

Aortic Valve Disease 1,Prostate Cancer,Bardet-Biedl Syndrome 7,Prostate Cancer, Hereditary, 12

Cannabis Dependence,Cholestasis, Intrahepatic, Of Pregnancy 3,Barrett'S Adenocarcinoma,Trachea Leiomyoma,Conjunctival Intraepithelial Neoplasm,Hyperoxaluria, Primary, Type Iii,Acute Promyelocytic Leukemia,Rectum Adenoma,Form Agnosia

Neurofibromatosis, Type Ii,Occipital Lobe Neoplasm,Peripheral Nerve Schwannoma,Hereditary Spherocytosis,Osteoporosis,Developmental And Epileptic Encephalopathy 5,West Syndrome,Beckwith-Wiedemann Syndrome,Spinocerebellar Ataxia 5

Isolated Unilateral Hemispheric Cerebellar Hypoplasia,Pachygyria,Sarcomatosis,Pilomyxoid Astrocytoma,Breast Cancer,Lissencephaly,Lissencephaly 9 With Complex Brainstem Malformation,Neuropathy, Hereditary Sensory And Autonomic, Type Vi

Myopathy,Congenital Nemaline Myopathy,Hypertrophic Cardiomyopathy,Breast Adenoid Cystic Carcinoma,Autosomal Dominant Macrothrombocytopenia,Dilated Cardiomyopathy,Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency,Focal Segmental Glomerulosclerosis,Bleeding Disorder, Platelet-Type, 15,Thrombocytopenia-Absent Radius Syndrome,Congenital Myasthenic Syndrome,Thrombocytopenia,Arrhythmogenic Right Ventricular Cardiomyopathy,Nonaka Myopathy,Myh-9 Related Disease

Subareolar Duct Papillomatosis,Infantile Digital Fibromatosis,Aortic Valve Disease 1,Nipple Benign Neoplasm,Aortic Aneurysm, Familial Thoracic 1,Marfan Syndrome

Bone Disease,Bone Development Disease,Cardiospondylocarpofacial Syndrome,Myofibrillar Myopathy,Synostosis,Subacute Lymphocytic Thyroiditis,Lethal Chondrodysplasia,Graves' Disease,Atelosteogenesis, Type I,Atelosteogenesis, Type Iii,Otopalatodigital Syndrome Spectrum Disorder,Frontometaphyseal Dysplasia,Idiopathic Bronchiectasis,Flnb Disorders,Spondylocarpotarsal Synostosis Syndrome,Boomerang Dysplasia,Congenital Knee Dislocation,Breast Cancer,Familial Hypercholesterolemia,Myopathy, Myofibrillar, 5,Gonadal Dysgenesis,Cleft Palate, Isolated,Seminal Vesicle Adenocarcinoma,Ear Malformation,Scheuermann Disease,Periventricular Nodular Heterotopia,Odontochondrodysplasia,Atelosteogenesis,Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations,Otopalatodigital Syndrome, Type Ii,Ischiocoxopodopatellar Syndrome With Or Without Pulmonary Arterial Hypertension,Melnick-Needles Syndrome,Larsen Syndrome,Scoliosis,Otopalatodigital Syndrome, Type I

Muscular Disease,X-Linked Recessive Disease,Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Cytoplasmic Body Myopathy,Amyotrophic Lateral Sclerosis 1,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d,Dystrophinopathies,Focal Segmental Glomerulosclerosis,Epidermolysis Bullosa Simplex With Muscular Dystrophy,Congenital Myasthenic Syndrome,Muscular Dystrophy, Becker Type,Walker-Warburg Syndrome,X-Linked Monogenic Disease,Cardiomyopathy, Dilated, 3b,Muscular Dystrophy, Duchenne Type,Muscular Dystrophy, Congenital Merosin-Deficient, 1a,Ullrich Congenital Muscular Dystrophy 1,Left Ventricular Noncompaction

Episodic Ataxia, Type 6,Cerebral Palsy,Episodic Ataxia,Spinocerebellar Ataxia 20,Mitochondrial Dna Depletion Syndrome 7,Episodic Ataxia, Type 2,Cerebellar Ataxia Type 9,Machado-Joseph Disease,Cerebellar Disease,Spastic Paraplegia 41, Autosomal Dominant,Spinocerebellar Ataxia 30,Spinocerebellar Ataxia, Autosomal Recessive 14,Boutonneuse Fever,Developmental And Epileptic Encephalopathy 5,Autosomal Dominant Cerebellar Ataxia,Spotted Fever,Brill-Zinsser Disease,West Syndrome,Disease Of Mental Health,Spinocerebellar Ataxia 23,Dentatorubral-Pallidoluysian Atrophy,Aceruloplasminemia,Spinocerebellar Ataxia, Autosomal Recessive 8,Israeli Tick Typhus,Far Eastern Spotted Fever,Rocky Mountain Spotted Fever,Beckwith-Wiedemann Syndrome,Spinocerebellar Ataxia 13,Cerebral Palsy, Ataxic, Autosomal Recessive,Epidemic Typhus,Endemic Typhus,Early Infantile Epileptic Encephalopathy,Spinocerebellar Ataxia 15,Familial Cold Autoinflammatory Syndrome 3,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spinocerebellar Ataxia 18,Microcephaly With Or Without Chorioretinopathy, Lymphedema, Or Mental Retardation,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Spinocerebellar Ataxia 5

Timothy Syndrome,Heart Disease,Intestinal Pseudo-Obstruction,Ovarian Endometrial Cancer,Brugada Syndrome 1,Cardiomyopathy, Dilated, 1e,Syncope,Pulmonary Valve Stenosis,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Erythromelalgia,Neuromuscular Junction Disease,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Palmoplantar Keratoderma And Congenital Alopecia 1,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Myocardial Infarction,Brugada Syndrome 5,Familial Long Qt Syndrome,Sick Sinus Syndrome 1,Paroxysmal Ventricular Fibrillation,Atrial Standstill,Developmental And Epileptic Encephalopathy 14,Familial Isolated Arrhythmogenic Right Ventricular Dysplasia,Familial Sick Sinus Syndrome,Neuroblastoma,Progressive Familial Heart Block,Long Qt Syndrome 12,Idiopathic Ventricular Fibrillation, Non Brugada Type,Isolated Elevated Serum Creatine Phosphokinase Levels,Atrial Standstill 1,Cardiovascular System Disease,Dilated Cardiomyopathy,Laminopathy,Sudden Infant Death Syndrome,Jervell And Lange-Nielsen Syndrome 1,Brugada Syndrome 6,Right Bundle Branch Block,Long Qt Syndrome,Malignant Hyperthermia,Left Bundle Branch Hemiblock,Heart Conduction Disease,Familial Periodic Paralysis,Progressive Familial Heart Block, Type Ia,Paroxysmal Extreme Pain Disorder,Paramyotonia Congenita Of Von Eulenburg,Ebstein Anomaly,Sick Sinus Syndrome,Lateral Myocardial Infarction,Andersen Cardiodysrhythmic Periodic Paralysis,Cardiac Arrhythmia,Cardiac Conduction Defect,Hypokalemic Periodic Paralysis, Type 1,Hyperkalemic Periodic Paralysis,Congestive Heart Failure,Long Qt Syndrome 13,Myasthenic Syndrome, Congenital, 5,Noonan Syndrome With Multiple Lentigines,Migraine, Familial Hemiplegic, 3,Disease Of Mental Health,Ventricular Fibrillation, Paroxysmal Familial, 1,Long Qt Syndrome 3,Long Qt Syndrome 2,Long Qt Syndrome 6,Long Qt Syndrome 5,Noonan Syndrome 7,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Congenital Myasthenic Syndrome,Left Ventricular Noncompaction 1,Keshan Disease,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Atrial Fibrillation, Familial, 10,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Supravalvular Aortic Stenosis,Brugada Syndrome 2,Long Qt Syndrome 9,Long Qt Syndrome 10,Brugada Syndrome 4,Tetralogy Of Fallot,Long Qt Syndrome 14,Distal Arthrogryposis,Familial Atrial Fibrillation,Early Infantile Epileptic Encephalopathy,Autosomal Genetic Disease,Short Qt Syndrome,Atrioventricular Block,First-Degree Atrioventricular Block,Second-Degree Atrioventricular Block,Third-Degree Atrioventricular Block,Sinoatrial Node Disease,Long Qt Syndrome 1,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Dravet Syndrome,Lipoprotein Quantitative Trait Locus,Generalized Epilepsy With Febrile Seizures Plus,Familial Hemiplegic Migraine,Atrial Fibrillation,Cardiac Arrest,Fetal Akinesia Deformation Sequence 1,Left Ventricular Noncompaction,Catecholaminergic Polymorphic Ventricular Tachycardia,Hereditary Lymphedema Ic,Epilepsy, Idiopathic Generalized,Cardiomyopathy, Dilated, 1b,Cardiac Arrhythmia, Ankyrin-B-Related

Esophagus Adenocarcinoma,Barrett'S Adenocarcinoma,Sialolithiasis,Maxillary Sinus Cancer,Neural Tube Defects,Paranasal Sinus Cancer

Epilepsy,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Autosomal Dominant Epilepsy With Auditory Features,Cerebral Amyloid Angiopathy, Itm2b-Related, 1,Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2,Alzheimer Disease 8,Epilepsy, Familial Temporal Lobe, 1

Muscular Dystrophy,Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency,Bruxism,Actn3 Deficiency,Congenital Myasthenic Syndrome,Glycogen Storage Disease V,Arrhythmogenic Right Ventricular Cardiomyopathy,Scoliosis

Primary Cutaneous T-Cell Lymphoma,Spinal Muscular Atrophy,Muscular Atrophy,Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency,Sezary'S Disease,Osteogenesis Imperfecta, Type Iv,Osteoporosis,Brittle Bone Disorder,Odontochondrodysplasia,Bone Mineral Density Quantitative Trait Locus 18,Osteogenesis Imperfecta, Type Xix,Childhood Spinal Muscular Atrophy,Spinal Muscular Atrophy, Type I,Spinal Muscular Atrophy, Type Iii,Spinal Muscular Atrophy, Type Ii,Mycosis Fungoides,Osteoporosis, Juvenile

Neuroblastoma,Sucrase-Isomaltase Deficiency, Congenital,Hirschsprung Disease 1,Attention Deficit-Hyperactivity Disorder,Neuroblastoma 1

Intestinal Pseudo-Obstruction,Atrophy Of Prostate,Aggressive Systemic Mastocytosis,Viral Gastritis,Benign Perivascular Tumor,Malignant Mesenchymoma,Cerebral Cavernous Malformations,Digeorge Syndrome,Glomuvenous Malformations,Aortic Aneurysm, Familial Thoracic 1,Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome,Lipoprotein Quantitative Trait Locus

Anterior Foramen Magnum Meningioma,Foramen Magnum Meningioma,Ovarian Cancer,Osteopetrosis,Prostatitis,Prostate Cancer,Glaucoma, Normal Tension

Muscular Disease,Brody Myopathy,Bone Structure Disease,Heart Disease,X-Linked Recessive Disease,Hemophagocytic Lymphohistiocytosis, Familial, 1,Congenital Fiber-Type Disproportion,Myoglobinuria,Retinitis Pigmentosa,Myopathy,Gas Gangrene,Myofibrillar Myopathy,Atrial Heart Septal Defect,Emery-Dreifuss Muscular Dystrophy,Muscle Tissue Disease,Exophthalmos,Neuromuscular Disease,Bethlem Myopathy 1,Hypertrophic Cardiomyopathy,Facioscapulohumeral Muscular Dystrophy 1,Symptomatic Form Of Muscular Dystrophy Of Duchenne And Becker In Female Carriers,Familial Isolated Dilated Cardiomyopathy,Progressive Muscular Dystrophy,Autosomal Dominant Distal Myopathy,Cytoplasmic Body Myopathy,Myositis,Interatrial Communication,Myotonic Dystrophy 1,Myopathy, Myofibrillar, 1,Extracardiac Rhabdomyoma,Spinal Muscular Atrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f,Retinal Ischemia,Tibial Muscular Dystrophy,Hypertrophic Pyloric Stenosis,Congenital Muscular Dystrophy-Dystroglycanopathy Type A,Isolated Elevated Serum Creatine Phosphokinase Levels,Reducing Body Myopathy,Interstitial Myocarditis,Myocarditis,Atrial Standstill 1,Cataract,Immunodeficiency 26,Dilated Cardiomyopathy,Dystrophinopathies,Glycogen Storage Disease,Fundus Dystrophy,Nr0b1-Related Adrenal Hypoplasia Congenita,Long Qt Syndrome,Malignant Hyperthermia,Muscular Dystrophy, Congenital, Lmna-Related,Cobblestone Lissencephaly,Localized Lipodystrophy,Waardenburg Syndrome, Type 4b,Eye Disease,Myopathy, Myofibrillar, 3,Colorectal Cancer,Peripheral Nervous System Disease,Pectus Excavatum,Cardiomyopathy, Familial Hypertrophic, 4,Endocardial Fibroelastosis,Myopathy, Myofibrillar, 5,Rhabdomyosarcoma,Rigid Spine Muscular Dystrophy 1,Respiratory Failure,Centronuclear Myopathy,Disease Of Mental Health,Adrenal Hypoplasia, Congenital,Creatine Phosphokinase, Elevated Serum,Glycogen Storage Disease Ii,Muscular Dystrophy, Becker Type,Oculomedin,Aland Island Eye Disease,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency,Schizophrenia,Restrictive Cardiomyopathy,Chromosome Xp21 Deletion Syndrome,Beckwith-Wiedemann Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Mcleod Syndrome,Lissencephaly,Walker-Warburg Syndrome,Muscle Hypertrophy,Nonaka Myopathy,Muscular Dystrophy-Dystroglycanopathy,X-Linked Monogenic Disease,Non-Syndromic X-Linked Intellectual Disability,Cardiomyopathy, Dilated, 3b,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome,Intrinsic Cardiomyopathy,Autism Spectrum Disorder,Glycerol Kinase Deficiency,Keratosis Follicularis Spinulosa Decalvans, X-Linked,Microcolon,Scoliosis,Ptosis,Muscular Dystrophy, Duchenne Type,Muscular Dystrophy, Congenital Merosin-Deficient, 1a,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2,Muscular Dystrophy-Dystroglycanopathy , Type A, 4,Ullrich Congenital Muscular Dystrophy 1,Retinoschisis 1, X-Linked, Juvenile,Left Ventricular Noncompaction,Autism,Batten-Turner Congenital Myopathy,Miyoshi Muscular Dystrophy,Multiple Pterygium Syndrome, Escobar Variant