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Nume Body Mass Index Quantitative Trait Locus 11
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Obesity due to excess calories; Obesity, unspecified; Other obesity
Clasificare anatomică Malacards Boli endocrine

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Aarskog-Scott Syndrome Abdominal Obesity-Metabolic Syndrome 1 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Acanthosis Nigricans Aceruloplasminemia Achalasia Achondroplasia Acinar Cell Carcinoma Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acrocallosal Syndrome Acromegaly Acth-Secreting Pituitary Adenoma Actinomycosis Acute Adrenal Insufficiency Acute Cor Pulmonale Acute Graft Versus Host Disease Acute Insulin Response Acute Leukemia Acute Mountain Sickness Acute Myocardial Infarction Acute Pancreatitis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Adenocarcinoma Adenoma Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adrenal Adenoma Adrenal Cortex Disease Adrenal Gland Disease Adrenal Gland Hyperfunction Adrenal Gland Pheochromocytoma Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete Adrenocortical Carcinoma, Hereditary Adult Lymphoma Adult-Onset Still's Disease Adult Respiratory Distress Syndrome Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Aland Island Eye Disease Alcohol Abuse Alcohol Dependence Alcoholic Hepatitis Alcoholic Pancreatitis Alexithymia Allergic Asthma Allergic Encephalomyelitis Allergic Hypersensitivity Disease Allergic Rhinitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alstrom Syndrome Alzheimer Disease 3 Amaurosis Fugax Amenorrhea Amyloidosis Anal Fistula Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Anencephaly Aneurysm Angelman Syndrome Angel-Shaped Phalangoepiphyseal Dysplasia Angina Pectoris Angiosarcoma Aniridia 1 Anisomastia Anorexia Nervosa 1 Anovulation Antiphospholipid Syndrome Aortic Aneurysm Aortic Atherosclerosis Aortic Coarctation Aplastic Anemia Apnea, Obstructive Sleep Apolipoprotein C-Iii Deficiency Apparent Mineralocorticoid Excess Appendicitis Arcus Corneae Arteries, Anomalies of Arteriosclerosis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Aspergillosis Aspiration Pneumonia Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atherosclerosis Susceptibility Atrial Fibrillation Atrichia with Papular Lesions Attention Deficit-Hyperactivity Disorder Atypical Depressive Disorder Aural Atresia, Congenital Autism Autism Spectrum Disorder Autoimmune Encephalitis Autoimmune Hepatitis Autoimmune Neuropathy Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autonomic Dysfunction Autonomic Neuropathy Ayazi Syndrome Ayme-Gripp Syndrome Azoospermia Back Pain Bardet-Biedl Syndrome Bardet-Biedl Syndrome 1 Bardet-Biedl Syndrome 10 Bardet-Biedl Syndrome 12 Bardet-Biedl Syndrome 2 Bardet-Biedl Syndrome 3 Bardet-Biedl Syndrome 6 Bardet-Biedl Syndrome 8 Barrett Esophagus B-Cell Lymphomas Beckwith-Wiedemann Syndrome Beriberi Biemond Syndrome Biemond Syndrome Ii Biliary Tract Disease Bipolar Disorder Bipolar I Disorder Bladder Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group, Junior System Blount's Disease Body Mass Index Quantitative Trait Locus 1 Body Mass Index Quantitative Trait Locus 10 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 Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borderline Personality Disorder Borna Disease Bornholm Eye Disease Brachydactyly Brain Cancer Breast Cancer Breast Disease Breast Reconstruction Bulimia Nervosa 1 Bulimia Nervosa 2 Buruli Ulcer Calcification of Joints and Arteries Calcinosis Calciphylaxis Camurati-Engelmann Disease Cannabis Dependence Capillary Hemangioma Cardiac Arrest Cardiac Conduction Defect Carnitine Deficiency, Systemic Primary Carnitine Palmitoyltransferase I Deficiency Carotid Artery Disease Carotid Intimal Medial Thickness 2 Carpal Tunnel Syndrome Cataract Cataract 5, Multiple Types Cauda Equina Syndrome Celiac Disease 1 Cellulitis Central Cord Syndrome Central Precocious Puberty Central Sleep Apnea Cerebral Artery Occlusion Cerebral Palsy Cerebritis Cerebrovascular Disease Ceroid Lipofuscinosis, Neuronal, 5 Cervical Cancer Cervical Intraepithelial Neoplasia Cervicitis Chagas Disease Chanarin-Dorfman Syndrome Charcot-Marie-Tooth Neuropathy Type 2a Chikungunya Childhood Leukemia Childhood Myocerebrohepatopathy Spectrum Cholangiocarcinoma Cholangitis Choledocholithiasis Cholelithiasis Cholestasis Chops Syndrome Chorioamnionitis Choroideremia Choroiditis Chromosome 1p36 Deletion Syndrome Chronic Fatigue Syndrome Chronic Laryngitis Chronic Pain Chronic Venous Insufficiency Ciliopathy Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Clear Cell Renal Cell Carcinoma Clopidogrel Resistance Cocaine Abuse Coffin-Lowry Syndrome Cohen-Gibson Syndrome Cohen Syndrome Colitis Colon Adenocarcinoma Colon Adenoma Colorectal Adenocarcinoma Colorectal Adenoma Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Conduct Disorder Congenital Bile Acid Synthesis Defect Congenital Disorder of Glycosylation, Type Iic Congenital Hypothyroidism Congenital Leptin Deficiency Congenitally Corrected Transposition of the Great Arteries Congestive Heart Failure Conjunctivitis Conn's Syndrome Constipation Corneal Dystrophy, Fleck Coronary Artery Aneurysm Coronary Artery Anomaly Coronary Heart Disease 1 Coronary Stenosis Corticosteroid-Binding Globulin Deficiency Cortisone Reductase Deficiency Cranial Nerve Malignant Neoplasm Craniopharyngioma Craniosynostosis with Fibular Aplasia Critical Illness Polyneuropathy Crouzon Syndrome Cystadenoma Cystic Fibrosis Cystic Kidney Disease Dacryoadenitis Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Degenerative Disc Disease Dementia Dental Caries Denys-Drash Syndrome Depersonalization Disorder Dermatitis Developmental Coordination Disorder Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus, Noninsulin-Dependent Diabetic Autonomic Neuropathy Diabetic Cataract Diabetic Foot Ulcers Diabetic Neuropathy Diabetic Polyneuropathy Diarrhea Diastolic Heart Failure Diastrophic Dysplasia Diffuse Idiopathic Skeletal Hyperostosis Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Diverticulitis Dock2 Deficiency Donnai-Barrow Syndrome Donohue Syndrome Double Discordia Down Syndrome Drug Dependence Ductal Carcinoma in Situ Dumping Syndrome Duodenal Ulcer Duodenitis Duodenogastric Reflux Dwarfism Dysbaric Osteonecrosis Dyspepsia Dysphagia Eating Disorder Eclampsia Ectopic Pregnancy Elephantiasis Empty Sella Syndrome Encephalocele Encephalopathy Endocrine Organ Benign Neoplasm Endocrine Pancreas Disease Endometrial Adenocarcinoma Endometrial Cancer Endotheliitis End Stage Renal Failure Entropion Epilepsy Epithelial Recurrent Erosion Dystrophy Esophageal Atresia Esophageal Cancer Estrogen-Receptor Negative Breast Cancer Estrogen-Receptor Positive Breast Cancer Euthyroid Sick Syndrome Exocrine Pancreatic Insufficiency Exophthalmos Familial Colorectal Cancer Familial Hyperlipidemia Familial Lcat Deficiency Familial Lipoprotein Lipase Deficiency Familial Partial Lipodystrophy Fanconi Anemia, Complementation Group E Fasciitis Fasting Hypoglycemia Fatty Liver Disease Fecal Incontinence Fetal Macrosomia Fibrocalculous Pancreatopathy Focal Segmental Glomerulosclerosis Fragile X Syndrome Friedreich Ataxia 1 Functional Gastric Disease Functioning Pituitary Adenoma Fundus Albipunctatus Galactorrhea Gallbladder Cancer Gallbladder Disease Gas Gangrene Gastric Adenocarcinoma Gastric Cancer Gastric Cardia Adenocarcinoma Gastric Dilatation Gastritis Gastroduodenitis Gastroesophageal Reflux Gastrointestinal System Disease Gastroparesis Genitopatellar Syndrome Gestational Diabetes Gigantism Gingivitis Glioma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glucagonoma Glucocorticoid Resistance, Generalized Glucose Intolerance Glucose Metabolism Disease Glycogen Storage Disease Goiter Gonadal Disease Gout Graft-Versus-Host Disease Granulomatous Hepatitis Growth Hormone Deficiency Growth Hormone Deficiency, Isolated Partial Growth Hormone Insensitivity, Partial Gynecomastia Halothane Hepatitis Headache Helicobacter Pylori Infection Helix Syndrome Hemangioma Hemophilia Hemophilia a Hemorrhagic Proctocolitis Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Adenoma Hepatocellular Carcinoma Hereditary Wilms' Tumor Hernia, Hiatus Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Histiocytosis Holoprosencephaly Homocysteinemia Homozygous Familial Hypercholesterolemia Horseshoe Kidney Human Immunodeficiency Virus Type 1 Hyaline Fibromatosis Syndrome Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hyperalphalipoproteinemia 1 Hyperandrogenism Hyperandrogenism Due to Cortisone Reductase Deficiency Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Familial Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 2 Hyperinsulinism Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hyperlipoproteinemia, Type V Hyperostosis Hyperparathyroidism Hyperpituitarism Hyperproinsulinemia Hyperprolactinemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Heart Disease Hyperthyroidism Hypertrichosis Hypertriglyceridemia, Familial Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Scars Hyperuricemia Hypoadrenalism Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypoglycemia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypolipoproteinemia Hypophosphatemic Bone Disease Hypopituitarism Hypospadias Hypothalamic Disease Hypotonia Hypoxia Ichthyosis Idiopathic Central Precocious Puberty Idiopathic Edema Idiopathic Recurrent Pericarditis Ige Responsiveness, Atopic Ileitis Immune-Complex Glomerulonephritis Immunodeficiency 40 Immunodeficiency, Common Variable, 10 Immunodeficiency with Hyper-Igm, Type 3 Immunoglobulin E Concentration, Serum Infant Gynecomastia Infertility Inflammatory Bowel Disease Influenza Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Insulinoma Intermittent Claudication Interstitial Lung Disease Intestinal Disease Intracranial Hypertension Intrahepatic Cholestasis Intussusception Irritable Bowel Syndrome Ischemia Ischemic Heart Disease Islet Cell Tumor Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Ib Isolated Growth Hormone Deficiency, Type Ii Janus Kinase-3 Deficiency Jejunoileitis Kawasaki Disease Keloids Keratoconjunctivitis Keratoconus Kidney Cancer Krukenberg Carcinoma Kwashiorkor Lactic Acidosis Langerhans Cell Histiocytosis Laron Syndrome Laryngeal Cleft Laryngitis Laugier-Hunziker Syndrome Learning Disability Lecithin:cholesterol Acyltransferase Deficiency Leopard Syndrome Leptin Receptor Deficiency Leptin, Serum Level of, Quantitative Trait Locus 1 Leukemia Leukodystrophy, Hypomyelinating, 3 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lichen Sclerosus Limb-Girdle Muscular Dystrophy Limb Ischemia Linitis Plastica Lipid Metabolism Disorder Lipid Storage Disease Lipodystrophy Lipodystrophy, Partial, Acquired Lipomatosis Lipomatosis, Multiple Symmetric Lipoprotein Glomerulopathy Lissencephaly 1 Liver Cirrhosis Liver Disease Logopenic Progressive Aphasia Long Qt Syndrome Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphadenitis Lymphedema Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphocytic Choriomeningitis Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphopenia Lymphosarcoma Lysosomal Acid Lipase Deficiency Malaria Male Infertility Malignant Hypertension Malignant Hyperthermia Marasmus Marfan Syndrome Maturity-Onset Diabetes of the Young Maturity-Onset Diabetes of the Young, Type 2 Mckusick-Kaufman Syndrome Mechanical Entropion Mediastinal Lipomatosis Mediastinitis Megaesophagus Megaloblastic Anemia Melanoma Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome Meralgia Paresthetica Metabolic Acidosis Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microtia Microvascular Complications of Diabetes 1 Microvascular Complications of Diabetes 5 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia Migraine with Aura Migraine with or Without Aura 1 Mitochondrial Disorders Mitochondrial Import-Stimulating Factor Mixed Cell Adenoma Mohr-Tranebjaerg Syndrome Momo Syndrome Monocytic Leukemia Monogenic Diabetes Mononeuropathy of the Median Nerve, Mild Mood Disorder Morbid Obesity Mucinous Adenocarcinoma Mucolipidosis Ii Alpha/beta Multinodular Goiter Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Personality Disorder Multiple Sclerosis Multiple Symmetrical Lipomatosis Mumps Mungan Syndrome Muscle Hypertrophy Muscular Dystrophy Myasthenia Gravis Myelodysplastic Syndrome Myeloid Leukemia Myelomeningocele Myocardial Infarction Myopathy Myxedema Narcolepsy Necrobiosis Lipoidica Nelson Syndrome Neonatal Meningitis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrosclerosis Nephrotic Syndrome Neural Crest Tumor Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurogenic Hypertension Neurogenic Thoracic Outlet Syndrome Neuromuscular Disease Neuronitis Neuropathy Neutropenia Neutrophil Actin Dysfunction Neutrophilia, Hereditary Niemann-Pick Disease Niemann-Pick Disease, Type B Night Blindness Nodular Nonsuppurative Panniculitis Nonalcoholic Steatohepatitis Nutritional Deficiency Disease Obesity, Hyperphagia, and Developmental Delay Obesity-Hypoventilation Syndrome Obstructive Hydrocephalus Occipital Horn Syndrome Omenn Syndrome Open-Angle Glaucoma Opioid Abuse Opitz Gbbb Syndrome, Type I Optic Nerve Hypoplasia, Bilateral Orofacial Cleft Osgood-Schlatter's Disease Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrosis Osteomalacia Osteopetrosis Osteoporotic Fracture Otitis Media Ouabain Resistance Ovarian Cancer Ovarian Cyst Ovarian Disease Overhydrated Hereditary Stomatocytosis Overnutrition Pachyonychia Congenita 1 Palmoplantar Carcinoma, Multiple Self-Healing Pancreas Disease Pancreatic Agenesis Pancreatic Cancer Pancreatic Cholera Pancreatitis Pancreatitis, Hereditary Pandas Papilledema Papillon-Lefevre Syndrome Papular Mucinosis Paraplegia Parathyroid Adenoma Patent Foramen Ovale Pathological Gambling Pediatric Hypertension Pediatric Multiple Sclerosis Pelvic Inflammatory Disease Penile Cancer Penis Agenesis Peptic Ulcer Disease Perinephritis Periodontal Disease Periodontitis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral Vascular Disease Peritonitis Perlman Syndrome Persistent Fetal Circulation Syndrome Personality Disorder Pertussis Pfeiffer Syndrome Phaeochromocytoma Pharyngitis Phelan-Mcdermid Syndrome Phenylketonuria Pheochromocytoma Pick Disease of Brain Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma Pituitary Adenoma 1, Multiple Types Pituitary Adenoma, Prolactin-Secreting Pituitary Carcinoma Pituitary-Dependent Cushing's Disease Pituitary Gland Disease Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Placental Abruption Placental Insufficiency Plantar Fasciitis Plasminogen Activator Inhibitor-1 Deficiency Plasmodium Falciparum Malaria Pneumatosis Cystoides Intestinalis Pneumonia Polycystic Ovary Syndrome Polycythemia Polydactyly Polydactyly, Postaxial, with Progressive Myopia Polyneuropathy Polysubstance Abuse Portal Hypertension Portal Vein Thrombosis Posterior Cerebral Artery Infarction Postgastrectomy Syndrome Postpartum Depression Post-Thrombotic Syndrome Post-Traumatic Stress Disorder Potocki-Lupski Syndrome Pouchitis Prader-Willi Syndrome Precocious Puberty Prediabetes Syndrome Pre-Eclampsia Premature Ejaculation Primary Hyperparathyroidism Primary Lateral Sclerosis, Adult, 1 Primitive Portal Vein Thrombosis Proopiomelanocortin Deficiency Prostate Cancer Prostate Disease Prostatitis Prosthetic Joint Infection Protein-Energy Malnutrition Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Pseudohypoparathyroidism, Type Ic Pseudopseudohypoparathyroidism Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulpitis Purpura Pycnodysostosis Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome Rapp-Hodgkin Syndrome Recurrent Acute Pancreatitis Refsum Disease, Classic Renal Infectious Disease Renal Osteodystrophy Resting Heart Rate, Variation in Restless Legs Syndrome Restrictive Cardiomyopathy Retinal Degeneration Retinal Dystrophy and Obesity Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome Retinitis Retinitis Pigmentosa Retinoschisis 1, X-Linked, Juvenile Reye Syndrome Rheumatic Disease Rheumatoid Arthritis Rhinitis Rohhad Salt and Pepper Developmental Regression Syndrome Sarcoidosis 2 Schizoaffective Disorder Schizophrenia Schnyder Corneal Dystrophy Schwartz-Jampel Syndrome, Type 1 Scleredema Sclerosing Cholangitis Secondary Adrenal Insufficiency Senile Cataract Sensorineural Hearing Loss Severe Combined Immunodeficiency Severe Pre-Eclampsia Sheehan Syndrome Short Bowel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sialadenitis Sick Building Syndrome Sickle Cell Anemia Sickle Cell Disease Siderosis Sinusitis Situs Inversus Sjogren-Larsson Syndrome Skeletal Dysplasias Skin Disease Sleep Apnea Sleep Disorder Slipped Capital Femoral Epiphysis Smith-Magenis Syndrome Social Phobia Spastic Cerebral Palsy Spasticity Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spinal Cord Injury Spinal Meningioma Spinal Stenosis Spondyloarthropathy Spondylolisthesis Spondyloocular Syndrome Squamous Cell Carcinoma Status Asthmaticus Steatorrhea Subacute Cerebellar Degeneration Substance Abuse Succinic Semialdehyde Dehydrogenase Deficiency Sudden Sensorineural Hearing Loss Superior Mesenteric Artery Syndrome Sveinsson Chorioretinal Atrophy Syncope Syndromic X-Linked Intellectual Disability 7 Synovitis Syringocystadenoma Papilliferum Systemic Lupus Erythematosus Systolic Heart Failure Takayasu Arteritis Tangier Disease Taqi Polymorphism T Cell Deficiency Tendinopathy Tendinosis Teratoma Testicular Microlithiasis Tetralogy of Fallot Thoracic Outlet Syndrome Three M Syndrome 1 Thrombocytopenia Thrombophilia Thrombophlebitis Thrombosis Thyroid Cancer Thyroiditis Tongue Cancer Tonsillitis Tracheal Stenosis Transposition of the Great Arteries Transsexualism Transsexuality Tremor Trochlear Dysplasia Turner Syndrome Uniparental Disomy of Chromosome 2 Uremia Uremic Pruritus Vaginitis Van Der Woude Syndrome 1 Varicocele Vascular Dementia Vascular Disease Vasculitis Venous Insufficiency Ventricular Fibrillation, Paroxysmal Familial, 1 Vertebrobasilar Insufficiency Viral Hepatitis Visceral Steatosis Vitamin B12 Deficiency Voyeurism Vulva Cancer Werner Syndrome Wernicke Encephalopathy Williams-Beuren Syndrome Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Wolffian Tumor Wolf-Hirschhorn Syndrome Woodhouse-Sakati Syndrome Xanthomatosis Yemenite Deaf-Blind Hypopigmentation Syndrome Zollinger-Ellison Syndrome