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Nume Heart Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice
Clasificari ICD10 Congenital malformation of heart, unspecified; Heart disease, unspecified; Heart failure, unspecified
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Congenital Heart Defects, Multiple Types, 2; Congenital Heart Defects, Multiple Types, 3; Congenital Heart Defects, Multiple Types, 4

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 46,xy Sex Reversal 3 47,xyy 48,xxyy Syndrome 49,xxxxy Syndrome Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Absence of the Pulmonary Artery Acanthosis Nigricans Acquired Amegakaryocytic Thrombocytopenia Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acquired Metabolic Disease Acquired Methemoglobinemia Acquired Thrombocytopenia Acquired Von Willebrand Syndrome Acrocallosal Syndrome Acromegaly Acute Mountain Sickness Acute Myocardial Infarction Acute Pyelonephritis Adams-Oliver Syndrome Adenocarcinoma Adenoid Hypertrophy Adenoiditis Adermatoglyphia Adrenocortical Carcinoma, Hereditary Adult Respiratory Distress Syndrome Afibrinogenemia, Congenital Aging Alagille Syndrome 1 Aland Island Eye Disease Alcohol Abuse Alcoholic Cardiomyopathy Alexithymia Al-Gazali-Bakalinova Syndrome Allergic Asthma Alopecia Alopecia, Androgenetic, 1 Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-1-Antitrypsin Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Capillary Dysplasia Alzheimer Disease 3 Amyloidosis Anal Atresia, Hypospadias, and Penoscrotal Inversion Analbuminemia Anauxetic Dysplasia 1 Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Angioedema Angiomatosis Aniridia 1 Anomalous Left Coronary Artery from the Pulmonary Artery Anorectal Anomalies Anorexia Nervosa 1 Anoxia Anterolateral Myocardial Infarction Antiphospholipid Syndrome Antipyrine Metabolism Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aortic Aneurysm, Familial Abdominal, 1 Aortic Coarctation Aortic Disease Aortic Valve Disease 2 Aortic Valve Insufficiency Aortopulmonary Window Apert Syndrome Aphthous Stomatitis Aplasia Cutis Congenita Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Apparent Mineralocorticoid Excess Arcus Corneae Argyria Arrhythmogenic Right Ventricular Cardiomyopathy Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Arterial Tortuosity Syndrome Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriosclerosis Obliterans Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Aspirin Resistance Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atherosclerosis Susceptibility Atrial Fibrillation Atrial Heart Septal Defect Atrial Septal Defect 4 Atrial Standstill Atrial Standstill 1 Atrioventricular Block Atrioventricular Septal Defect Attention Deficit-Hyperactivity Disorder Aural Atresia, Congenital Autoimmune Disease Autoimmune Myocarditis Autoinflammation with Infantile Enterocolitis Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Axenfeld-Rieger Syndrome Ayme-Gripp Syndrome Bacterial Meningitis Bardet-Biedl Syndrome 2 Bardet-Biedl Syndrome 6 Benign Adult Familial Myoclonic Epilepsy Benign Essential Hypertension Beriberi Bestrophinopathy, Autosomal Recessive Beukes Hip Dysplasia Biliary Atresia Bladder Disease Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blue Toe Syndrome Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bornholm Eye Disease Brachydactyly Brain Injury Branchial Cleft Anomalies Breast Cancer Brittle Bone Disorder Bronchiolitis Bronchogenic Cyst Bronchopneumonia Bronchopulmonary Dysplasia Brugada Syndrome Budd-Chiari Syndrome Buerger Disease Bullous Impetigo Burns Buruli Ulcer Candida Glabrata Carcinoid Syndrome Carcinoid Tumors, Intestinal Cardiac Arrest Cardiac Arrhythmia Cardiac Arrhythmia, Ankyrin-B-Related Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiac Sarcoidosis Cardiofaciocutaneous Syndrome 1 Cardiogenic Shock Cardiomyopathy, Dilated, 1e Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Infantile Hypertrophic Carotid Artery Disease Carotid Intimal Medial Thickness 2 Carotid Stenosis Cataract Catecholaminergic Polymorphic Ventricular Tachycardia Cavernous Lymphangioma Centralopathic Epilepsy Central Retinal Vein Occlusion Central Serous Chorioretinopathy Central Sleep Apnea Cerebral Atherosclerosis Cerebral Hemorrhage Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cervicitis Chagas Disease Charge Syndrome Char Syndrome Chlamydia Chlorpropamide-Alcohol Flushing Choanal Atresia, Posterior Cholangitis Cholelithiasis Chondrodysplasia Punctata Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromosomal Triplication Chromosome 15q11.2 Deletion Syndrome Chromosome 15q Deletion Chromosome 16p13.3 Duplication Syndrome Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb Chromosome 22q11.2 Duplication Syndrome Chromosome 2p Duplication Chromosome 3p Deletion Chromosome 5q Duplication Chromosome 6q Deletion Chromosome 8p23.1 Deletion Chromosome 8p Duplication Chromosome 8q Duplication Chromosome 9p Deletion Syndrome Chronic Angina Chronic Kidney Failure Chronic Pulmonary Heart Disease Chronic Thromboembolic Pulmonary Hypertension Chronic Venous Insufficiency Churg-Strauss Syndrome Ciliopathy Cleft Lip Cleft Lip/palate Clopidogrel Resistance Collecting Duct Carcinoma Colobomatous Microphthalmia Colorblindness, Partial, Protan Series Colorectal Cancer Colpocephaly Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Congenital Heart Defects, Dysmorphic Facial Features, and Intellectual Developmental Disorder Congenital Hepatic Fibrosis Congenital Hypothyroidism Congenital Lymphedema Congenital Rubella Congenital Subglottic Stenosis Congenital Tracheal Stenosis Congenital Varicella Syndrome Congestive Heart Failure Conjunctivitis Connective Tissue Disease Conotruncal Heart Malformations Constipation Constrictive Pericarditis Cor Biloculare Cornelia De Lange Syndrome Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Restenosis Coronary Stenosis Coronary Thrombosis Corpus Callosum, Agenesis of, with Abnormal Genitalia Cortical Blindness Cor Triatriatum Cor Triatriatum Dexter Craniorachischisis Craniosynostosis Creutzfeldt-Jakob Disease Cri-Du-Chat Syndrome Crimean-Congo Hemorrhagic Fever Critical Congenital Heart Disease Crouzon Syndrome with Acanthosis Nigricans Cutaneous Lupus Erythematosus Cutis Laxa, Autosomal Recessive, Type Iiia Cyanosis, Transient Neonatal Cystitis Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dandy-Walker Complex Dandy-Walker Syndrome Darier-White Disease Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Defective Apolipoprotein B-100 Dementia Dengue Hemorrhagic Fever Denys-Drash Syndrome Dermatitis Dermatitis Herpetiformis Dermatomyositis Dextrocardia Dextrocardia with Situs Inversus Dextro-Looped Transposition of the Great Arteries Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Angiopathy Diaphragmatic Eventration Diaphragmatic Hernia, Congenital Diastolic Heart Failure Diastrophic Dysplasia Diencephalic Syndrome Diffuse Lymphatic Malformation Digeorge Syndrome Dilated Cardiomyopathy Discrete Subaortic Stenosis Double Discordia Double-Orifice Mitral Valve Double Outlet Left Ventricle Down Syndrome Duane Retraction Syndrome Duane Retraction Syndrome 1 Duodenal Atresia Duodenitis Dysautonomia Dysostosis Ebstein Anomaly Eclampsia Ectrodactyly Cardiopathy Dysmorphism Eisenmenger Syndrome Ellis-Van Creveld Syndrome Emphysema, Congenital Lobar Encephalocele Encephalomyopathy Endocardial Fibroelastosis Endocarditis Endocardium Disease Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Enhanced S-Cone Syndrome Enterocolitis Epilepsy Erythromelalgia Esophageal Atresia Esophageal Atresia/tracheoesophageal Fistula Esterase C Euthyroid Sick Syndrome Exfoliation Syndrome Extra-Adrenal Pheochromocytoma Extrinsic Cardiomyopathy Fabry Disease Facial Hemiatrophy Facial Paralysis Factor Viii Deficiency Factor X Deficiency Familial Bicuspid Aortic Valve Familial Deafness Familial Hyperlipidemia Familial Hypertension Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form Familial Isolated Dilated Cardiomyopathy Familial Long Qt Syndrome Familial Short Qt Syndrome Fanconi Anemia, Complementation Group E Fatty Liver Disease Fetal Hydantoin Syndrome Fibromuscular Dysplasia Fournier Gangrene Frontonasal Dysplasia Phocomelic Upper Limbs Galactose Epimerase Deficiency Gallbladder Disease Gastric Ulcer Gastritis Gastroschisis Gaucher Disease, Type I Generalized Anxiety Disorder Generalized Atherosclerosis Genitopatellar Syndrome Gestational Diabetes Gilbert Syndrome Gingival Fibromatosis Gitelman Syndrome Glomerulonephritis Glucose Intolerance Glucose Metabolism Disease Glucose Transporter Type 1 Deficiency Syndrome Goiter Goldberg-Shprintzen Syndrome Gout Griscelli Syndrome Growth Hormone Deficiency Gynecomastia Hallermann-Streiff Syndrome Headache Head Injury Heart Block, Congenital Heart Cancer Heart Conduction Disease Heart Defects, Congenital, and Other Congenital Anomalies Heart Septal Defect Helicobacter Pylori Infection Hemangioma Hemifacial Microsomia Hemihyperplasia, Isolated Hemoglobinopathy Hemoglobinuria Hemopericardium Hemophilia Hemophilia a Hemophilia B Hemorrhage, Intracerebral Hemorrhagic Disease Hemorrhagic Fever Hemorrhoid Hemosiderosis Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatopulmonary Syndrome Hepatorenal Syndrome Hereditary Spherocytosis Heterotaxy Heterotaxy, Visceral, 1, X-Linked His Bundle Tachycardia Holoprosencephaly Holt-Oram Syndrome Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homozygous Familial Hypercholesterolemia Hyaline Fibromatosis Syndrome Hydrocephalus Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperalphalipoproteinemia 1 Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyperglycemia Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hyperostosis Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertensive Retinopathy Hyperthyroidism Hypertriglyceridemia, Familial Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hyperuricemia Hypoaldosteronism Hypoalphalipoproteinemia, Primary Hypocomplementemic Urticarial Vasculitis Hypogonadism Hypokalemia Hypomelanotic Disorder Hypoplastic Left Heart Syndrome Hypoplastic Left Heart Syndrome 1 Hyporeninemic Hypoaldosteronism Hypothyroidism, Congenital, Nongoitrous, 4 Hypoxia Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis Prematurity Syndrome Idiopathic Edema Idiopathic Hemiconvulsion-Hemiplegia Syndrome Igg4-Related Disease Immune System Disease Immunoglobulin E Concentration, Serum Infant Gynecomastia Infective Endocarditis Inferior Vena Cava Interruption Inflammatory Bowel Disease Influenza Inguinal Hernia Inherited Blood Coagulation Disease Insulin-Like Growth Factor I Interatrial Communication Intermittent Claudication Interstitial Cystitis Interstitial Emphysema Interstitial Lung Disease Interstitial Nephritis Intestinal Disease Intestinal Impaction Intestinal Perforation Intracranial Hypertension Intracranial Thrombosis Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Intrinsic Cardiomyopathy Ischemia Ischemic Heart Disease Ischemic Optic Neuropathy Isolated Congenitally Uncorrected Transposition of the Great Arteries Jervell and Lange-Nielsen Syndrome 1 Johanson-Blizzard Syndrome Kallmann Syndrome Kasznica Carlson Coppedge Syndrome Kawasaki Disease Kbg Syndrome Keshan Disease Klippel-Feil Syndrome Korean Hemorrhagic Fever Kwashiorkor Kyphoscoliotic Heart Disease Lacrimoauriculodentodigital Syndrome Lactic Acidosis Lambert Syndrome Late-Onset Focal Dermal Elastosis Leech Infestation Left Ventricular Noncompaction Lemierre's Syndrome Leopard Syndrome Leptospirosis Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukomalacia Levocardia Limb Ischemia Lipid Metabolism Disorder Lipomatosis, Multiple Liposarcoma Lissencephaly Lissencephaly 1 Liver Cirrhosis Liver Disease Loeys-Dietz Syndrome Logopenic Progressive Aphasia Long Qt Syndrome Long Qt Syndrome 1 Long Qt Syndrome 12 Long Qt Syndrome 13 Long Qt Syndrome 2 Long Qt Syndrome 3 Long Qt Syndrome 5 Long Qt Syndrome 6 Lung Agenesis Lung Cancer Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphangioma Lymphangiomatosis Lymphedema Lymphoma Lymphopenia Malaria Malignant Essential Hypertension Malignant Hypertension Malignant Otitis Externa Malignant Secondary Hypertension Malignant Spiradenoma Marantic Endocarditis Marden-Walker Syndrome Marfan Syndrome Mast Cell Activation Syndrome Mature Teratoma Mcdonough Syndrome Mckusick-Kaufman Syndrome Meckel Syndrome, Type 1 Mediastinitis Megaesophagus Menkes Disease Mental Depression Mesenteric Vascular Occlusion Methemoglobinemia Microcephalic Osteodysplastic Primordial Dwarfism, Type I Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microphthalmia Microtia Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Midline Cervical Cleft Migraine with Aura Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Mitochondrial Encephalomyopathy Mitral Valve Disease Mitral Valve Insufficiency Mitral Valve Stenosis Miyoshi Muscular Dystrophy 1 Moderate and Severe Traumatic Brain Injury Moebius Syndrome Mohr-Tranebjaerg Syndrome Mood Disorder Morbid Obesity Mosaic Trisomy 9 Moyamoya Disease 1 Mucolipidosis Ii Alpha/beta Mucopolysaccharidoses Mucopolysaccharidosis, Type Vii Mucositis Multiple Sclerosis Multisystemic Smooth Muscle Dysfunction Syndrome Mungan Syndrome Muscle Hypertrophy Muscular Atrophy Mutism Mycobacterium Chelonae Mycoplasmal Pneumonia Myelitis Myelodysplastic Syndrome Myocardial Infarction Myocardial Stunning Myocarditis Myopathy Myopia Myosin Storage Myopathy Myositis Myotonia Myotonia Atrophica Myxedema Neonatal Diabetes Mellitus Nephrosclerosis Netherton Syndrome Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neutrophil Actin Dysfunction Non-a-E Hepatitis Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Nutritional Deficiency Disease Obstructive Jaundice Occipital Encephalocele Ochronosis Oculodentodigital Dysplasia Oliver Syndrome Omenn Syndrome Omphalocele Open-Angle Glaucoma Opitz Gbbb Syndrome, Type I Orofacial Cleft Orofaciodigital Syndrome I Orofaciodigital Syndrome Viii Orotic Aciduria Orthostatic Intolerance Orthostatic Proteinuria Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteoporosis-Pseudoglioma Syndrome Ovarian Cancer Overnutrition Paine Syndrome Pallister-Killian Mosaic Syndrome Pallister-Killian Syndrome Pancreatic Agenesis Pancreatitis Panic Disorder Papilledema Papillon-Lefevre Syndrome Parametritis Paraplegia Paroxysmal Cold Hemoglobinuria Patau Syndrome Patent Ductus Arteriosus 1 Patent Ductus Venosus Patent Foramen Ovale Pathological Gambling Pectus Excavatum Pentalogy of Cantrell Peptic Ulcer Disease Pericardial Effusion Pericardial Mesothelioma Pericarditis Perinephritis Periodontal Disease Periodontitis Periostitis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral Vascular Disease Peripheral Vertigo Peritonitis Periventricular Leukomalacia Persistent Fifth Aortic Arch Peutz-Jeghers Syndrome Pharyngitis Phelan-Mcdermid Syndrome Phenylketonuria Pheochromocytoma Pierre Robin Syndrome Plagiocephaly Plastic Bronchitis Pneumonia Polycystic Kidney Disease Polycystic Ovary Syndrome Polycythemia Polydactyly Polydactyly, Postaxial, Type A1 Polydactyly, Postaxial, with Progressive Myopia Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polyneuropathy Polyvalvular Heart Disease Syndrome Portal Hypertension Portal Vein Thrombosis Posterior Urethral Valves Postherpetic Neuralgia Post-Traumatic Stress Disorder Postural Hypotension Potocki-Lupski Syndrome Precocious Puberty Prediabetes Syndrome Pre-Eclampsia Primary Ciliary Dyskinesia Primary Lateral Sclerosis, Adult, 1 Progressive Familial Heart Block Progressive Familial Heart Block, Type Ib Propionic Acidemia Prostate Cancer Prostatitis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Prothrombin Deficiency Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak Pseudovaginal Perineoscrotal Hypospadias Pseudoxanthoma Elasticum Pseudoxanthoma Elasticum-Like Papillary Dermal Elastolysis Psoriasis Psoriasis 13 Psoriatic Arthritis Psychotic Disorder Pulmonary Alveolar Microlithiasis Pulmonary Alveolar Proteinosis Pulmonary Aspergilloma Pulmonary Atresia with Intact Ventricular Septum Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Emphysema Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonary Interstitial Glycogenosis Pulmonary Valve Disease Pulmonary Valve Stenosis Pulmonary Vein Stenosis Pulmonic Stenosis Purpura Pyelonephritis Pyloric Stenosis Pyoderma Qualitative Platelet Defect Radial Hemimelia Ramer Ladda Syndrome Raynaud Disease Reactive Arthritis Renal Artery Disease Renal Artery Obstruction Renal Dysplasia Renal Glucosuria Renal Hypertension Renal Tubular Acidosis Renal Tubular Dysgenesis Renovascular Hypertension Respiratory Syncytial Virus Infectious Disease Resting Heart Rate, Variation in Restless Legs Syndrome Restrictive Cardiomyopathy Retinal Artery Occlusion Retroperitoneal Fibrosis Rheumatic Disease Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatic Heart Disease Rheumatoid Arthritis Rhizomelic Chondrodysplasia Punctata Right Aortic Arch Right Bundle Branch Block Ring Chromosome 11 Ring Chromosome 13 Ring Chromosome 4 Ring Chromosome 7 Robinow Syndrome Rubella Rubeosis Iridis Saal Bulas Syndrome Sagittal Sinus Thrombosis Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Satb2-Associated Syndrome Scalp-Ear-Nipple Syndrome Scarlet Fever Schizophrenia Sclerocornea Scoliosis Secondary Hypertrophic Osteoarthropathy Secondary Pulmonary Hemosiderosis Seminoma Shone Complex Short Qt Syndrome Short Stature, Developmental Delay, and Congenital Heart Defects Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sickle Cell Anemia Sickle Cell Disease Sick Sinus Syndrome Silver-Russell Syndrome Single Ventricular Heart Sinoatrial Node Disease Situs Inversus Skeletal Dysplasias Sleep Apnea Sleep Disorder Smith-Lemli-Opitz Syndrome Smith-Magenis Syndrome Sotos Syndrome 1 Spasticity Spinal Cord Infarction Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spiradenoma Split Foot Split Hand Split Hand-Foot Malformation Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondylocostal Dysostosis 1, Autosomal Recessive Spondylocostal Dysostosis 3, Autosomal Recessive Spondylocostal Dysostosis 5 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Status Epilepticus Sternal Cleft Stomatitis Stroke, Ischemic Subacute Bacterial Endocarditis Subclavian Artery Aneurysm Subendocardial Myocardial Infarction Sudden Arrhythmia Death Syndrome Sudden Sensorineural Hearing Loss Supravalvular Aortic Stenosis Sveinsson Chorioretinal Atrophy Syncope Syndactyly, Type Iii Syndrome of Inappropriate Antidiuretic Hormone Systemic Lupus Erythematosus Systemic Scleroderma Systolic Heart Failure Takayasu Arteritis Tangier Disease T Cell Deficiency Teratocarcinoma Teratoma Tetralogy of Fallot Thalassemia Thoracoabdominal Syndrome Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thymic Dysplasia Thyroid Crisis Thyroiditis Tick Paralysis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tonsillitis Tooth Agenesis Torticollis Toxic Myocarditis Tracheal Stenosis Tracheobronchomalacia Tracheoesophageal Fistula Transient Global Amnesia Transposition of the Great Arteries Tricuspid Atresia Tricuspid Valve Disease Tricuspid Valve Insufficiency Tricuspid Valve Stenosis Tropical Endomyocardial Fibrosis Turner Syndrome Twin-to-Twin Transfusion Syndrome Univentricular Heart Uremia Urinary System Disease Vacterl Association Vaginal Atresia Vaginitis Van Der Woude Syndrome 1 Varicose Veins Vascular Dementia Vascular Disease Vasculitis Vasculogenic Impotence Vein Disease Velocardiofacial Syndrome Venous Insufficiency Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy Visceral Heterotaxy Vitamin E, Familial Isolated Deficiency of Von Willebrand Disease, Type 1 Wolff-Parkinson-White Syndrome Xanthomatosis X-Linked Opitz G/bbb Syndrome Xp22.3 Microdeletion Syndrome