Migraine With Or Without Aura 1,Dental Anomalies And Short Stature,Nystagmus 2, Congenital, Autosomal Dominant,Migraine With Aura,Acute Interstitial Pneumonia,Wolfram Syndrome,Bipolar Disorder,Disease Of Mental Health,Schizophrenia,Migraine, Familial Hemiplegic, 1,Familial Hemiplegic Migraine,Acrofacial Dysostosis,Acrofacial Dysostosis 1, Nager Type

Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,X-Linked Cerebellar Ataxia,Deafness, Autosomal Dominant 58,Crouzon Syndrome With Acanthosis Nigricans,Spinocerebellar Ataxia, X-Linked 3,Spinocerebellar Ataxia, X-Linked 4,Spinocerebellar Ataxia, X-Linked 1

Ataxia, Sensory, 1, Autosomal Dominant,Cone-Rod Dystrophy 10

Alzheimer Disease 15,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Ventricular Tachycardia, Catecholaminergic Polymorphic, 2,Syndromic Intellectual Disability

Factor Xiii Deficiency,Hemorrhagic Disease,Prothrombin Deficiency,Hemarthrosis,Brachydactyly, Type D,Factor V And Factor Viii, Combined Deficiency Of, 1,Factor V Deficiency,Factor V And Factor Viii, Combined Deficiency Of, 2,Thrombocytopenia,Venezuelan Hemorrhagic Fever,Factor Viii Deficiency,Good Syndrome

Pityriasis Versicolor,Alzheimer Disease,Breast Cancer,Epidermodysplasia Verruciformis 1,Skin Carcinoma,Schneiderian Carcinoma,Epidermodysplasia Verruciformis 3

Hypertension, Diastolic,Bacterial Pneumonia,Episodic Ataxia, Type 4,Attention Deficit-Hyperactivity Disorder

Tinea Nigra,Drug Psychosis,Drug-Induced Mental Disorder,Blastomycosis,Substance-Induced Psychosis,Spinal Cord Lymphoma,Mucolipidosis Iii Gamma

Liver Disease,Bile Duct Disease,Citrullinemia, Classic,Amino Acid Metabolic Disorder,Urea Cycle Disorder,Fatty Liver Disease,Biliary Tract Disease,Brain Edema,Developmental And Epileptic Encephalopathy 39,Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss, Autosomal Recessive,Bilirubin Metabolic Disorder,Hepatic Encephalopathy,Cholestasis,Obstructive Jaundice,Citrullinemia, Type Ii, Adult-Onset,Galactosemia I,Asperger Syndrome,Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome,Hypermethioninemia,Citrullinemia, Type Ii, Neonatal-Onset,3-Methylcrotonyl-Coa Carboxylase Deficiency,Autosomal Recessive Disease,Mitochondrial Dna Depletion Syndrome 3,Bile Acid Synthesis Defect, Congenital, 1,Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To,Argininemia,Argininosuccinic Aciduria,Carnitine Deficiency, Systemic Primary

Alzheimer Disease,Familial Adult Myoclonic Epilepsy,Diamond-Blackfan Anemia 10,Diamond-Blackfan Anemia 20,Niemann-Pick Disease, Type C2,Ceroid Lipofuscinosis, Neuronal, 3

Chronic Tic Disorder,Alzheimer Disease 15

Macs Syndrome,Hepatocellular Carcinoma

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

Bone Disease,Fibrous Dysplasia,Dentinogenesis Imperfecta,Aortic Valve Disease 2,Calcinosis,Melorheostosis,Chondrosarcoma,Myositis Ossificans,Tongue Carcinoma,Fibrosarcomatous Osteosarcoma,Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor,Quebec Platelet Disorder,Paget'S Disease Of Bone,Osteogenesis Imperfecta, Type Iv,Osseous Heteroplasia, Progressive,Osteoporosis,Aplastic Anemia,Ovarian Cancer,Breast Cancer,Open-Angle Glaucoma,Papillary Cystadenocarcinoma,Cystadenocarcinoma,Hepatocellular Carcinoma,Clear Cell Chondrosarcoma,Lateral Cystocele,Mccune-Albright Syndrome,Extraosseous Osteosarcoma,Bone Osteosarcoma,Conventional Central Osteosarcoma,Root Resorption,Cone-Rod Dystrophy 2,Prostate Cancer,Brittle Bone Disorder,Pulmonary Fibrosis, Idiopathic,Thrombocytopenia,Pericoronitis,Odontochondrodysplasia,Gray Platelet Syndrome,Vitreoretinopathy, Neovascular Inflammatory,Osteogenesis Imperfecta, Type Xvii,Meningioma, Familial,Osteofibrous Dysplasia,Osteoblastoma,Lung Cancer,Osteogenic Sarcoma,Osteoporosis, Juvenile,Pancreatic Cancer,Pseudoxanthoma Elasticum,Pycnodysostosis

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

Fibrosclerosis Of Breast,Lymphoproliferative Syndrome, X-Linked, 1

Alzheimer Disease,Branchiootorenal Syndrome 2

Retinitis Pigmentosa,Polyposis Syndrome, Hereditary Mixed, 1,Xeroderma Pigmentosum Group E,Hereditary Mixed Polyposis Syndrome,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group G,Xeroderma Pigmentosum, Complementation Group B,Ck Syndrome,Trichothiodystrophy 3, Photosensitive,Uv-Sensitive Syndrome,Bardet-Biedl Syndrome 1,Joubert Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia