Timothy Syndrome,Heart Disease,Brugada Syndrome 1,Syncope,Neuromuscular Junction Disease,Neuromuscular Disease,Gastroparesis,Hypertrophic Cardiomyopathy,Rasopathy,Hypokalemia,Familial Long Qt Syndrome,Developmental And Epileptic Encephalopathy 14,Progressive Familial Heart Block,Long Qt Syndrome 12,Dilated Cardiomyopathy,Sudden Infant Death Syndrome,Jervell And Lange-Nielsen Syndrome 1,Right Bundle Branch Block,Long Qt Syndrome,Malignant Hyperthermia,Heart Conduction Disease,Familial Short Qt Syndrome,Andersen Cardiodysrhythmic Periodic Paralysis,Cardiac Arrhythmia,Acute Diffuse Nephritis,Fainting,Long Qt Syndrome 13,Short Qt Syndrome 1,Myasthenic Syndrome, Congenital, 5,Noonan Syndrome With Multiple Lentigines,Disease Of Mental Health,Long Qt Syndrome 3,Long Qt Syndrome 2,Long Qt Syndrome 6,Long Qt Syndrome 5,Body Mass Index Quantitative Trait Locus 11,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Congenital Myasthenic Syndrome,Schizophrenia,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Hypotrichosis 1,Arrhythmogenic Right Ventricular Dysplasia, Familial, 12,Supravalvular Aortic Stenosis,Chromosome 2q35 Duplication Syndrome,Long Qt Syndrome 9,Brugada Syndrome 4,Tetralogy Of Fallot,Long Qt Syndrome 14,Familial Atrial Fibrillation,Early Infantile Epileptic Encephalopathy,Short Qt Syndrome,Atrioventricular Block,First-Degree Atrioventricular Block,Third-Degree Atrioventricular Block,Sinoatrial Node Disease,Long Qt Syndrome 1,Cardiomyopathy, Familial Hypertrophic, 1,Intrinsic Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Cardiac Arrest,Properdin Deficiency, X-Linked,Left Ventricular Noncompaction,Catecholaminergic Polymorphic Ventricular Tachycardia,Cardiac Arrhythmia, Ankyrin-B-Related

Ciliary Dyskinesia, Primary, 18,Primary Ciliary Dyskinesia,Prkar1b-Related Neurodegenerative Dementia With Intermediate Filaments,Spinal Cord Astrocytoma,Carney Complex Variant,Familial Atrial Fibrillation,Ciliary Dyskinesia, Primary, 1,Primary Pigmented Nodular Adrenocortical Disease

Carney Complex Variant,Melanotic Neurilemmoma,Kallmann Syndrome,Primary Pigmented Nodular Adrenocortical Disease

Acromesomelic Dysplasia,Hyperphenylalaninemia,Cystic Fibrosis,Chromosome 4q21 Deletion Syndrome,Secretory Diarrhea,Odontochondrodysplasia

Pseudopseudohypoparathyroidism,Growth Hormone Secreting Pituitary Adenoma,Pseudohypoparathyroidism,Acrodysostosis 1 With Or Without Hormone Resistance,Heart Cancer,Cowden Syndrome,Sex Cord-Gonadal Stromal Tumor,Adrenal Adenoma,Adenoma,Dysostosis,Pseudohypoparathyroidism, Type Ia,Conn'S Syndrome,Adrenal Gland Disease,Acth-Secreting Pituitary Adenoma,Basophil Adenoma,Amelogenesis Imperfecta,Carney Complex, Type 1,Breast Ductal Adenoma,Parathyroid Adenoma,Acth-Independent Macronodular Adrenal Hyperplasia,Hyperpituitarism,Acromegaly,Idiopathic Hypercalciuria,Carney Complex Variant,Thyroid Tumor,Pituitary Gland Disease,Hypoplastic Amelogenesis Imperfecta,Acth-Independent Cushing Syndrome,Functioning Pituitary Adenoma,Autoimmune Hypoparathyroidism,Osseous Heteroplasia, Progressive,Osteoporosis,Hypothyroidism, Congenital, Nongoitrous, 1,Hyperparathyroidism,Hormone Producing Pituitary Cancer,Acrodysostosis With Multiple Hormone Resistance,Multiple Endocrine Neoplasia,Amelogenesis Imperfecta Hypoplastic Type, Ig,Lipomatosis,Neurilemmoma,Neurilemmomatosis,Melanotic Neurilemmoma,Mccune-Albright Syndrome,Peutz-Jeghers Syndrome,Hypoparathyroidism,Primary Hyperparathyroidism,Acrodysostosis,Sertoli Cell Tumor,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Pigmented Nodular Adrenocortical Disease, Primary, 1,Adrenal Cortical Carcinoma,Breast Adenoma,Usher Syndrome, Type Iv,Pituitary Adenoma,Multiple Endocrine Neoplasia, Type Iv,Adrenal Carcinoma,Rapp-Hodgkin Syndrome,Adrenal Cortex Disease,Thyroid Gland Follicular Carcinoma,Beckwith-Wiedemann Syndrome,Multiple Endocrine Neoplasia, Type I,Usher Syndrome,Odontochondrodysplasia,Brachydactyly,Acute Promyelocytic Leukemia,Paraganglioma And Gastric Stromal Sarcoma,Adrenal Cortical Adenoma,Meningioma, Familial,Breast Benign Neoplasm,Endocrine Organ Benign Neoplasm,Thoracic Benign Neoplasm,Lentigines,Primary Pigmented Nodular Adrenocortical Disease,Amelogenesis Imperfecta, Type Ig,Li-Fraumeni Syndrome,Thyroid Carcinoma, Familial Medullary,Myxoma, Intracardiac,Pituitary Adenoma, Prolactin-Secreting

Heart Disease,Atrial Heart Septal Defect,Hypertrophic Cardiomyopathy,Renal Tuberculosis,Familial Sick Sinus Syndrome,Progressive Familial Heart Block,Isolated Elevated Serum Creatine Phosphokinase Levels,Sick Sinus Syndrome 2,Dilated Cardiomyopathy,Brugada Syndrome 8,Right Bundle Branch Block,Long Qt Syndrome,Heart Conduction Disease,Ebstein Anomaly,Sick Sinus Syndrome,Myasthenic Syndrome, Congenital, 5,Long Qt Syndrome 2,Congenital Myasthenic Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Long Qt Syndrome 9,Familial Atrial Fibrillation,Atrioventricular Block,Second-Degree Atrioventricular Block,Third-Degree Atrioventricular Block,Sinoatrial Node Disease,Long Qt Syndrome 1,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Cardiac Arrest,Left Ventricular Noncompaction,Catecholaminergic Polymorphic Ventricular Tachycardia

Myopathy,Impotence,Connective Tissue Disease,Diabetes Mellitus,Aortic Dissection,Alzheimer Disease,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Cystic Fibrosis,Aortic Disease,Aortic Valve Disease 1,Heritable Thoracic Aortic Disease,Hemolytic Anemia,Non-Proliferative Fibrocystic Change Of The Breast,Aneurysm,Aortic Aneurysm, Familial Thoracic 8,Disease Of Mental Health,Pulmonary Hypertension,Body Mass Index Quantitative Trait Locus 11,Aortic Aneurysm,Loeys-Dietz Syndrome,Immune Deficiency Disease,Myelodysplastic Syndrome,Attention Deficit-Hyperactivity Disorder,Aortic Aneurysm, Familial Thoracic 1,Hypertension, Essential,Sexual Disorder

Schizoid Personality Disorder