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

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

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

Breast Giant Fibroadenoma

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

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

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

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

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

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

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

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

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

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

Ebola Hemorrhagic Fever,Diffuse Idiopathic Skeletal Hyperostosis,Distal Hereditary Motor Neuronopathy Type 7,Perry Syndrome,Fanconi Anemia, Complementation Group A,Neuronopathy, Distal Hereditary Motor, Type Viib,Joubert Syndrome 1

Immunodeficiency 14,Non-Syndromic X-Linked Intellectual Disability