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Boli A-Z Abdominal Tuberculosis Abducens Palsy Abetalipoproteinemia Acalculous Cholecystitis Acanthosis Nigricans Acatalasemia Aceruloplasminemia Acetyl-Coa Acetyltransferase-2 Deficiency Achalasia Acid Sphingomyelinase Deficiency Acinar Cell Carcinoma Acquired Amegakaryocytic Thrombocytopenia Acquired Angioedema Acquired Generalized Lipodystrophy Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acrodermatitis Acromegaly Actinic Lichen Planus Actinomycosis Acute Adrenal Insufficiency Acute Cholangitis Acute Diarrhea Acute Disseminated Encephalomyelitis Acute Generalized Exanthematous Pustulosis Acute Graft Versus Host Disease Acute Insulin Response Acute Interstitial Pneumonia Acute Leukemia Acute Liver Failure Acute Lymphocytic Leukemia Acute Motor and Sensory Axonal Neuropathy Acute Motor Axonal Neuropathy Acute Myocardial Infarction Acute Myocarditis Acute Pancreatitis Acute Porphyria Acute Promyelocytic Leukemia Acute Pyelonephritis Acute Salpingitis Acute T Cell Leukemia Acute Thyroiditis Acute Transverse Myelitis Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of Adenocarcinoma Adenofibroma Adenoiditis Adenoma Adenomatoid Tumor Adenomyoma Adenosarcoma Adenosine Deaminase Deficiency Adenosquamous Carcinoma Adie Pupil Adiponectin, Serum Level of, Quantitative Trait Locus 1 Adiposis Dolorosa Adrenal Carcinoma Adrenal Cortical Adenoma Adrenal Neuroblastoma Adrenal Rest Tumor Adult-Onset Still's Disease Adult Respiratory Distress Syndrome Adult T-Cell Leukemia Afferent Loop Syndrome Afibrinogenemia Agammaglobulinemia Aggressive Systemic Mastocytosis Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Alagille Syndrome 1 Al Amyloidosis Aland Island Eye Disease Alcohol Abuse Alcohol Dependence Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alcoholic Pancreatitis Alexithymia Alkaptonuria Allantoicase Allergic Asthma Alopecia Alopecia, Androgenetic, 1 Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Totalis Alopecia Universalis Congenita 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 Alstrom Syndrome Alveolar Echinococcosis Alzheimer Disease 3 Amebiasis Amelanotic Melanoma Amelogenesis Imperfecta Hypomaturation Type Aminoaciduria Aminoacylase 1 Deficiency Amyloid Neuropathy Amyloidosis Amyloidosis, Hereditary, Transthyretin-Related Amyotrophic Neuralgia Analbuminemia Anaplastic Large Cell Lymphoma Anauxetic Dysplasia 1 Anca-Associated Vasculitis Ancylostomiasis Androgen Insensitivity Syndrome, Mild Aneurysm Angelman Syndrome Angel-Shaped Phalangoepiphyseal Dysplasia Angiodysplasia Angioedema Angioimmunoblastic T-Cell Lymphoma Angiolipoma Angiomatosis Angiomyolipoma Angiomyoma Angiosarcoma Aniridia 1 Ankylosis Annular Erythema Anorexia Nervosa 1 Anosmia Anoxia Anterior Cutaneous Nerve Entrapment Syndrome Anterior Uveitis Anthracosilicosis Anthracosis Antiphospholipid Syndrome Antipyrine Metabolism Antisynthetase Syndrome Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aortic Atherosclerosis Aortic Coarctation Aortic Disease Aortitis Aphasia Aphthous Stomatitis Aplasia of Lacrimal and Salivary Glands Aplastic Anemia Apolipoprotein C-Ii Deficiency Apolipoprotein C-Iii Deficiency Appendicitis Appendix Adenocarcinoma Argininemia Argininosuccinic Aciduria Arteries, Anomalies of Arteriolosclerosis Arteriosclerosis Arteriovenous Fistula Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 5 Arthrogryposis, Distal, Type 9 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Arthus Reaction Ascaridiasis Ascending Cholangitis Ascending Colon Cancer Aseptic Meningitis Aspergillosis Asphyxia Neonatorum Asphyxiating Thoracic Dystrophy Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Telangiectasia Atherosclerosis Susceptibility Atrial Fibrillation Atrophic Gastritis Attention Deficit-Hyperactivity Disorder Atypical Teratoid Rhabdoid Tumor Australia Antigen Autoimmune Disease Autoimmune Enteropathy Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Myocarditis Autoimmune Pancreatitis Autoimmune Polyendocrine Syndrome Autoimmune Polyendocrine Syndrome Type 1 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autoinflammation with Infantile Enterocolitis Autonomic Dysfunction Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Axenfeld-Rieger Syndrome Axonal Neuropathy Ayme-Gripp Syndrome Bacillary Angiomatosis Back Pain Banti's Syndrome Bardet-Biedl Syndrome Barrett Esophagus Bartonellosis Basidiobolomycosis B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beckwith-Wiedemann Syndrome Bernard-Soulier Syndrome Bestrophinopathy, Autosomal Recessive Beta-Thalassemia Bilateral Massive Adrenal Hemorrhage Bile Duct Carcinoma Bile Duct Cysts Biliary Atresia Biliary Hypoplasia Biliary Papillomatosis Biliary Tract Disease Biliary Tract Neoplasm Black Hairy Tongue Blackwater Fever Bladder Adenocarcinoma Bladder Cancer Bladder Disease Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Bohring-Opitz Syndrome Bone Fracture Bone Marrow Failure Syndrome 1 Bone Marrow Necrosis Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borderline Leprosy Bornholm Eye Disease Boutonneuse Fever Brain Cancer Brain Edema Brain Ischemia Brain Small Vessel Disease with or Without Ocular Anomalies Branchiootic Syndrome 1 Branch Retinal Artery Occlusion Breast Cancer Brody Myopathy Bronchiolitis Bronchiolitis Obliterans Bronchogenic Cyst Bronchopneumonia Brucellosis Budd-Chiari Syndrome Bullous Lichen Planus Bullous Pemphigoid Burkitt Lymphoma Burning Mouth Syndrome Burns Bursitis Buruli Ulcer Calcinosis Candidiasis Capillariasis Capillary Hemangioma Capillary Leak Syndrome Capillary Malformation-Arteriovenous Malformation Carbonic Anhydrase Va Deficiency Carcinoid Syndrome Carcinoid Tumors, Intestinal Cardiac Arrest Cardiac Conduction Defect Cardiac Tamponade Cardiogenic Shock Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cardiomyopathy, Familial Hypertrophic, 1 Carney Triad Carnitine Palmitoyltransferase I Deficiency Caroli Disease Carotid Artery Disease Carotid Artery Occlusion Carpal Tunnel Syndrome Cartilage Disease Catamenial Pneumothorax Cataract Cataract 2, Multiple Types Cataract 40 Cataract Congenital Dominant Non Nuclear Cataract, Total Congenital Catastrophic Antiphospholipid Syndrome Cat Eye Syndrome Cat-Scratch Disease Cavernous Hemangioma Cavernous Lymphangioma Cavernous Malformation Celiac Disease 1 Cellulitis Central Nervous System Disease Central Nervous System Lymphoma Central Nervous System Vasculitis Central Pontine Myelinolysis Central Retinal Vein Occlusion Cerebellar Degeneration-Related Autoantigen 3 Cerebellar Hypoplasia Cerebral Aneurysms Cerebral Atrophy Cerebral Degeneration Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebrotendinous Xanthomatosis Cerebrovascular Disease Cervical Cancer Cervicitis Chagas Disease Chanarin-Dorfman Syndrome Chediak-Higashi Syndrome Chickenpox Chilaiditi Syndrome Childhood Hepatocellular Carcinoma Childhood Leukemia Childhood Medulloblastoma Chlamydia Cholangiocarcinoma Cholangiolocellular Carcinoma Cholangitis Cholecystitis Cholecystolithiasis Choledocholithiasis Cholelithiasis Cholestasis Cholestasis-Lymphedema Syndrome Cholesterol Ester Storage Disease Choline Deficiency Disease Chondroblastic Osteosarcoma Chondrodysplasia Punctata Syndrome Chondrosarcoma, Extraskeletal Myxoid Chops Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioamnionitis Chorioangioma Choriocarcinoma Chorioretinitis Choroiditis Chromophobe Renal Cell Carcinoma Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome Xp21 Deletion Syndrome Chronic Active Epstein-Barr Virus Infection Chronic Cholangitis Chronic Enteropathy Associated with Slco2a1 Gene Chronic Fatigue Syndrome Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Intestinal Vascular Insufficiency Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids Chronic Mucocutaneous Candidiasis Chronic Pyelonephritis Churg-Strauss Syndrome Ciguatera Fish Poisoning Ciliopathy Citrullinemia, Type Ii, Adult-Onset Citrullinemia, Type Ii, Neonatal-Onset Clear Cell Renal Cell Carcinoma Cleft Larynx, Posterior Clonorchiasis Clopidogrel Resistance Clostridium Perfringens Infection Clostridium Septicum Infection Coach Syndrome Cocaine Intoxication Coccidioidomycosis Coccidiosis Cocoon Syndrome Cohen-Gibson Syndrome Cold Agglutinin Disease Cold Urticaria Colitis Collagen Disease Collagenous Colitis Collagen Type Iii Glomerulopathy Collecting Duct Carcinoma Coloboma, Ocular, Autosomal Recessive Colon Adenocarcinoma Colonic Disease Colon Leiomyosarcoma Colorado Tick Fever Colorblindness, Partial, Protan Series Colorectal Adenocarcinoma Colorectal Adenoma Colorectal Cancer Common Mesentery Common Variable Immunodeficiency Communicating Hydrocephalus Compartment Syndrome Complement Component 4a Deficiency Complement Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Congenital Bronchobiliary Fistula Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Ib Congenital Disorder of Glycosylation, Type Iic Congenital Generalized Lipodystrophy Congenital Giant Megaureter Congenital Hemolytic Anemia Congenital Hepatic Fibrosis Congenital Herpes Simplex Congenital Human Immunodeficiency Virus Congenital Hypothyroidism Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Portosystemic Shunt Congenital Rubella Congenital Syphilis Congenital Tricuspid Stenosis Congestive Heart Failure Conjunctivitis Connective Tissue Disease Conotruncal Heart Malformations Constricting Bands, Congenital Constrictive Pericarditis Contact Dermatitis Coproporphyria, Hereditary Coronary Arterial Fistulas Cortical Blindness Corticosteroid-Binding Globulin Deficiency Cranial Nerve Palsy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crescentic Glomerulonephritis Crest Syndrome Crigler-Najjar Syndrome, Type I Crouzon Syndrome with Acanthosis Nigricans Cryoglobulinemia Cryoglobulinemia, Familial Mixed Cryptococcosis Cryptogenic Cirrhosis Cryptosporidiosis Culler-Jones Syndrome Cutaneous Lupus Erythematosus Cutaneous Mastocytosis Cutaneous Polyarteritis Nodosa Cutaneous Porphyria Cutaneous T Cell Lymphoma Cyanosis, Transient Neonatal Cyclic Neutropenia Cyclic Vomiting Syndrome Cystadenocarcinoma Cystadenoma Cystathioninuria Cystic Echinococcosis Cysticercosis Cystic Fibrosis Cystic Lymphangioma Cystic Teratoma Cystinosis Cystitis Cytochrome P450 2d6 Variant Cytomegalic Inclusion Disease Cytomegalovirus Infection Dacryoadenitis Dandy-Walker Complex Deafness-Hypogonadism Syndrome Dementia Demyelinating Disease Demyelinating Polyneuropathy Dendritic Cell Tumor Dengue Hemorrhagic Fever Dengue Shock Syndrome Dengue Virus Dermal Ridges-off-the-End Dermatitis Dermatitis Herpetiformis Dermatitis Herpetiformis, Familial Dermatomyositis Dermatophytosis Desmoid Tumor Desmoplastic Small Round Cell Tumor Desquamative Interstitial Pneumonia Dextrocardia Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diaphragmatic Eventration Diaphragmatic Hernia, Congenital Diarrhea Diarrhea 2, with Microvillus Atrophy Diffuse Large B-Cell Lymphoma Diffuse Neonatal Hemangiomatosis Dilated Cardiomyopathy Diphtheria Dirofilariasis Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Distomatosis Diverticulitis Donnai-Barrow Syndrome Double Inferior Vena Cava Down Syndrome Drug Dependence Drug-Induced Hepatitis Drug Rash with Eosinophilia and Systemic Symptoms Duane Retraction Syndrome 1 Dubin-Johnson Syndrome Duodenal Atresia Duodenal Obstruction Duodenal Ulcer Duodenitis Dwarfism Dysautonomia Dyskeratosis Congenita Dyskeratosis Congenita, X-Linked Dysphagia Dystonia Echinococcosis Eclampsia Ectopic Pregnancy Eczema Herpeticum Ehlers-Danlos Syndrome Ehrlichiosis Ellis-Van Creveld Syndrome Embryonal Rhabdomyosarcoma Embryonal Sarcoma Emphysematous Cholecystitis Encephalitis Encephalocele Encephalomalacia Encephalopathy Endocarditis Endometrial Adenocarcinoma Endometrial Stromal Nodule Endometriosis Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Enterocolitis Eosinophilia-Myalgia Syndrome Eosinophilic Colitis Eosinophilic Fasciitis Eosinophilic Gastroenteritis Eosinophilic Granuloma Eosinophilic Granulomatosis with Polyangiitis Eosinophilic Pneumonia Eosinophilic Pustular Folliculitis Epidermodysplasia Verruciformis Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epidermolysis Bullosa Dystrophica, Autosomal Recessive Epidermolysis Bullosa Pruriginosa Epidermolytic Hyperkeratosis Epidural Abscess Epilepsy Epileptic Encephalopathy, Early Infantile, 6 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Epithelial-Myoepithelial Carcinoma Epithelial Recurrent Erosion Dystrophy Epithelioid Hemangioendothelioma Epstein-Barr Virus Hepatitis Erdheim-Chester Disease Erysipelas Erythema Infectiosum Erythema Multiforme Esophageal Tuberculosis Esophageal Varix Euthyroid Sick Syndrome Evans' Syndrome Exanthem Exfoliative Dermatitis Exocrine Pancreatic Insufficiency Exophthalmos Extrahepatic Cholestasis Extrapontine Myelinolysis Extrapulmonary Tuberculosis Factor X Deficiency Factor Xiii Deficiency Fainting Familial Adenomatous Polyposis Familial Adenomatous Polyposis 1 Familial Lipoprotein Lipase Deficiency Familial Mediterranean Fever Familial Partial Lipodystrophy Familial Porphyria Cutanea Tarda Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fasciitis Fascioliasis Fasting Hypoglycemia Fatty Liver Disease Feingold Syndrome 1 Fibrillary Glomerulonephritis Fibrocalculous Pancreatopathy Fibrolamellar Carcinoma Fibromatosis, Gingival, 1 Fibromuscular Dysplasia Fibrosarcoma Fibrosing Mediastinitis Fibrous Dysplasia Fibrous Histiocytoma Fibular Hypoplasia and Complex Brachydactyly Fitz-Hugh-Curtis Syndrome Focal Epilepsy Focal Segmental Glomerulosclerosis Follicular Dendritic Cell Sarcoma Follicular Lymphoma Folliculitis Folliculotropic Mycosis Fungoides Foot Drop Fragile X Syndrome Friedreich Ataxia 1 Frontotemporal Dementia, Chromosome 3-Linked Fructosuria, Essential Fucosidosis Fulminant Viral Hepatitis Fundus Albipunctatus Galactose Epimerase Deficiency Galactosemia Gallbladder Cancer Gallbladder Disease Ganglioneuroblastoma Ganglioneuroma Gardner-Diamond Syndrome Gas Gangrene Gastric Adenocarcinoma Gastric Cancer Gastric Dilatation Gastric Lymphoma Gastric Ulcer Gastrinoma Gastritis Gastroduodenitis Gastroenteritis Gastroesophageal Reflux Gastrointestinal Neuroendocrine Tumor Gastrointestinal Stromal Tumor Gastrointestinal System Disease Gastroschisis Gender Identity Disorder Generalized Anxiety Disorder Genitopatellar Syndrome Germ Cells Tumors Gestational Choriocarcinoma Gestational Trophoblastic Tumor Gianotti Crosti Syndrome Giant Hemangioma Giardioză Gigantism Gilbert Syndrome Gilles De La Tourette Syndrome Gingivitis Glanzmann Thrombasthenia Glaucoma-Related Pigment Dispersion Syndrome Glioma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomangioma Glomerulonephritis Glucagonoma Glucocorticoid Resistance, Generalized Glucose Intolerance Glucose Metabolism Disease Glucosephosphate Dehydrogenase Deficiency Glucosephosphate Isomerase Deficiency Glucose Transporter Type 1 Deficiency Syndrome Glutathione Synthetase Deficiency Glycerol Kinase Deficiency Glycine N-Methyltransferase Deficiency Glycogen Storage Disease Glycogen Storage Disease 0, Liver Glycogen Storage Disease Ia Glycogen Storage Disease Iii Glycogen Storage Disease Ixa1 Glycogen Storage Disease Viii Glycoproteinosis Gout Graft-Versus-Host Disease Granular Cell Tumor Granulocytopenia Granuloma Annulare Granulomatous Angiitis Granulomatous Dermatitis Granulomatous Gastritis Granulomatous Hepatitis Granulosa Cell Tumor of the Ovary Graves' Disease Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Guillain-Barre Syndrome Guillain-Barre Syndrome, Familial Haemophilus Influenzae Hair Disease Hairy Cell Leukemia Hairy Tongue Halothane Hepatitis Hansen's Disease Hashimoto Thyroiditis Headache Associated with Sexual Activity Helicobacter Pylori Infection Helix Syndrome Hellp Syndrome Hemangioblastoma Hemangioendothelioma Hemangioma Hemangioma of Liver Hemangiopericytoma, Malignant Hematopoietic Stem Cell Transplantation Hemihyperplasia, Isolated Hemiplegia Hemochromatosis, Neonatal Hemochromatosis, Type 1 Hemochromatosis, Type 4 Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemorrhagic Proctocolitis Hemorrhagic Shock and Encephalopathy Syndrome Hemosiderosis Henoch-Schoenlein Purpura Hepadnavirus Infection Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Angiomyolipoma Hepatic Coma Hepatic Encephalopathy Hepatic Infarction Hepatic Lipase Deficiency Hepatic Tuberculosis Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatic Venoocclusive Disease with Immunodeficiency Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis D Hepatitis E Hepatoblastoma Hepatocellular Adenoma Hepatocellular Carcinoma Hepatoid Adenocarcinoma Hepatoportal Sclerosis Hepatopulmonary Syndrome Hepatorenal Syndrome Hepatosplenic T-Cell Lymphoma Hereditary Amyloidosis Hereditary Elliptocytosis Hereditary Hemorrhagic Telangiectasia Hereditary Spherocytosis Hermaphroditism Heroin Dependence Herpes Simplex Herpes Simplex Encephalitis Herpes Zoster Heterotaxy Heterotaxy, Visceral, 1, X-Linked Hfe-Associated Hereditary Hemochromatosis Histiocytic Sarcoma Histiocytoma Histiocytosis Histiocytosis-Lymphadenopathy Plus Syndrome Histoplasmosis Homocysteinemia Homocystinuria Homozygous Familial Hypercholesterolemia Horns in Sheep Human Coronavirus Sensitivity Human Granulocytic Anaplasmosis Human Herpesvirus 8 Human Immunodeficiency Virus Type 1 Human Monocytic Ehrlichiosis Human T-Cell Leukemia Virus Type 1 Huntington Disease-Like 2 Huntington Disease-Like 3 Hydranencephaly Hydrocephalus Hydrolethalus Syndrome 1 Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hyperalphalipoproteinemia 1 Hyperandrogenism Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyperglycemia Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinemic Hypoglycemia, Familial, 6 Hyperinsulinism Hyperlipidemia, Familial Combined Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome Hyperostosis Hyperoxaluria, Primary, Type Ii Hyperparathyroidism Hypersensitivity Reaction Type Iii Disease Hypersensitivity Vasculitis Hypersomnia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hyperthyroidism Hyperthyroxinemia Hypertrichosis Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hyperuricemia Hypervitaminosis a Hypoadrenalism Hypoascorbemia Hypocalcemia, Autosomal Dominant 1 Hypochondriasis Hypochondroplasia Hypochromic Microcytic Anemia with Iron Overload Hypocomplementemic Urticarial Vasculitis Hypoglycemia Hypoglycemic Coma Hypogonadism Hypokalemia Hypolipoproteinemia Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatasia Hypophosphatasia, Adult Hypophosphatasia, Infantile Hypophosphatemia Hypopituitarism Hypotonia Hypotonia-Cystinuria Syndrome Hypotrichosis 1 Hypoxia Ichthyosis Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis Ichthyosis Prematurity Syndrome Idiopathic Peliosis Hepatis Iga Glomerulonephritis Igg4-Related Disease Igg4-Related Hepatopathy Igg4-Related Sclerosing Cholangitis Ileal Neuroendocrine Tumor Ileocolitis Ileum Cancer Immune-Complex Glomerulonephritis Immune Suppression Immunodeficiency 43 Immunodeficiency with Hyper-Igm, Type 3 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Immunotactoid Glomerulopathy Immunotactoid or Fibrillary Glomerulopathy Inclusion Body Myositis Incontinentia Pigmenti Indian Tick Typhus Indolent B Cell Lymphoma Infantile Myofibromatosis Infective Endocarditis Infertility Inflammatory Bowel Disease Inflammatory Myofibroblastic Tumor Influenza Inguinal Hernia Inosine Triphosphatase Deficiency Insulin Autoimmune Syndrome Insulin-Like Growth Factor I Insulinoma Interstitial Lung Disease Interstitial Nephritis Intervertebral Disc Disease Intestinal Atresia Intestinal Disease Intestinal Perforation Intestinal Pseudo-Obstruction Intestinal Schistosomiasis Intestinal Volvulus Intracranial Hypertension Intrahepatic Bile Duct Adenoma Intrahepatic Biliary Papillomatosis Intrahepatic Cholangiocarcinoma Intrahepatic Cholestasis Intrauterine Infections Intravascular Large B-Cell Lymphoma Intravascular Papillary Endothelial Hyperplasia Intussusception Invasive Aspergillosis Irinotecan Toxicity Iritis Iron Metabolism Disease Iron Overload in Africa Ischemia Ischemic Neuropathy Ischemic Optic Neuropathy Islet Cell Tumor Isolated Congenital Hepatic Fibrosis Isolated Growth Hormone Deficiency, Type Ia Isolated Optic Neuritis Isovaleric Acidemia Japanese Encephalitis Japanese Spotted Fever Jejunoileitis Johanson-Blizzard Syndrome Juvenile Rheumatoid Arthritis Juvenile Xanthogranuloma Kabuki Syndrome 1 Kaposi Sarcoma Kawasaki Disease Keratoconjunctivitis Keratoconjunctivitis Sicca Kernicterus Keshan Disease Kidney Cancer Kid Syndrome Kindler Syndrome Klatskin's Tumor Kniest Dysplasia Kwashiorkor Lactic Acidosis Large Granular Lymphocyte Leukemia Larsen Syndrome Laryngeal Cleft Lassa Fever Laurence-Moon Syndrome Leber Congenital Amaurosis Lecithin:cholesterol Acyltransferase Deficiency Left-Sided Gallbladder Leiomyoma Leiomyosarcoma Leishmaniasis Lennox-Gastaut Syndrome Lepromatous Leprosy Leptospirosis Leukemia Leukemia, Acute Lymphoblastic 3 Leukodystrophy, Hypomyelinating, 5 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukoplakia Leukostasis Lewis-Sumner Syndrome Lichen Nitidus Lichen Planus Lichen Planus Pemphigoides Lichen Planus Pigmentosus Lichen Sclerosus Lichen Sclerosus Et Atrophicus Light Chain Deposition Disease Linear Iga Disease Linear Lichen Planus Linitis Plastica Lipase Deficiency, Combined Lipid Metabolism Disorder Lipoblastoma Lipodystrophy Lipodystrophy, Congenital Generalized, Type 2 Lipogranulomatosis Lipoid Congenital Adrenal Hyperplasia Lipoid Nephrosis Lipomatosis Lipomatosis, Multiple Lipomatosis, Multiple Symmetric Liposarcoma Lissencephaly 1 Listeria Meningitis Listeriosis Livedoid Vasculopathy Liver Angiosarcoma Liver Cirrhosis Liver Disease Liver Inflammatory Pseudotumor Liver Lymphoma Liver Sarcoma Lobomycosis Localized Scleroderma Logopenic Progressive Aphasia Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lung Cancer Lung Disease Lung Giant Cell Carcinoma Lupus Erythematosus Lupus Erythematosus Panniculitis Lyme Disease Lymphadenitis Lymphangiectasia, Intestinal Lymphangiectasis Lymphangioleiomyomatosis Lymphangioma Lymphangiomatosis Lymphoblastic Leukemia Lymphocele Lymphocytic Choriomeningitis Lymphocytic Colitis Lymphocytic Vasculitis Lymphoepithelioma-Like Carcinoma Lymphogranuloma Venereum Lymphoid Interstitial Pneumonia Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphopenia Lymphoplasmacytic Lymphoma Lymphoproliferative Syndrome Lymphosarcoma Lysinuric Protein Intolerance Lysosomal Acid Lipase Deficiency Macrocytic Anemia Macroglobulinemia Macrophage Activation Syndrome Macs Syndrome Macular Dystrophy, Retinal, 1, North Carolina Type Malakoplakia Malaria Malignant Epithelioid Hemangioendothelioma Malignant Germ Cell Tumor Malignant Glioma Malignant Histiocytosis Malignant Hypertension Malignant Mesenchymoma Malignant Peripheral Nerve Sheath Tumor Malignant Peritoneal Mesothelioma Malignant Triton Tumor Mallory-Weiss Syndrome Manganese Poisoning Mantle Cell Lymphoma Maple Syrup Urine Disease Marasmus Marfan Syndrome Marginal Zone B-Cell Lymphoma Mast Cell Activation Syndrome Mastitis Maturity-Onset Diabetes of the Young Maturity-Onset Diabetes of the Young, Type 3 Measles Meconium Ileus Mediastinitis Medullary Sponge Kidney Medulloblastoma Megacolon Megakaryocytic Leukemia Megaloblastic Anemia Melanoma Melanoma Metastasis Melioidosis Melkersson-Rosenthal Syndrome Membranoproliferative Glomerulonephritis Membranous Nephropathy Meninges Hemangiopericytoma Meningitis Meningococcal Infection Meningococcemia Meningoencephalitis Menkes Disease Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mercury Poisoning Mesangial Proliferative Glomerulonephritis Mesenchymal Cell Neoplasm Mesenchymoma Metabolic Acidosis Metastatic Insulinoma Methemoglobinemia Methionine Adenosyltransferase Deficiency Mevalonic Aciduria Microcytic Anemia Microscopic Polyangiitis Microsporidiosis Microtia-Anotia Migraine with or Without Aura 1 Milia, Multiple Eruptive Miliary Tuberculosis Mirizzi Syndrome Mitochondrial Complex I Deficiency Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 4a Mixed Connective Tissue Disease Mixed Cryoglobulinemia Type Iii Miyoshi Muscular Dystrophy 1 Molluscum Contagiosum Monocarboxylate Transporter 1 Deficiency Monoclonal Gammopathy of Uncertain Significance Monocytic Leukemia Mononeuritis Multiplex Mononeuropathy Mood Disorder Morbid Obesity Mosaic Genome-Wide Paternal Uniparental Disomy Mosaic Trisomy 14 Mouth Disease Mucinous Adenocarcinoma Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Mucositis Muir-Torre Syndrome Multidrug-Resistant Tuberculosis Multifocal Choroiditis Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Pterygium Syndrome, Lethal Type Multiple Sclerosis Multiple Sclerosis 2 Mumps Mungan Syndrome Muscle Disorders Muscular Dystrophy Myasthenia Gravis Mycobacterium Chelonae Mycobacterium Fortuitum Mycobacterium Kansasii Mycobacterium Xenopi Mycosis Fungoides Myelitis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myocardial Infarction Myocarditis Myoclonus Myoclonus Epilepsy Myoma Myopathy Myopathy, X-Linked, with Excessive Autophagy Myopericytoma Myositis Myospherulosis Myotonia Congenita, Autosomal Dominant Myxedema Myxoid Leiomyosarcoma Nail Disorder, Nonsyndromic Congenital, 7 Nasopharyngeal Carcinoma Nasopharyngitis Natural Killer Cell Leukemia Necrobiotic Xanthogranuloma Necrotizing Fasciitis Neonatal Diabetes Mellitus Neonatal Herpes Neonatal Hypothyroidism Neonatal Jaundice Neonatal Lupus Erythematosus Neovascular Glaucoma Nephrogenic Systemic Fibrosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephronophthisis Nephronophthisis 11 Nephronophthisis 3 Nephrotic Syndrome Nervous System Disease Neuritis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibroma Neurofibromatosis, Type Ii Neurofibromatosis, Type Iv, of Riccardi Neuroma Neuromyelitis Optica Neuromyelitis Optica Spectrum Disorder Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neuroretinitis Neurosarcoidosis Neurosyphilis Neutropenia Neutrophil Actin Dysfunction Neutrophil Migration Newcastle Disease Niemann-Pick Disease Niemann-Pick Disease, Type B Nodal Marginal Zone B-Cell Lymphoma Nodular Lymphocyte Predominant Hodgkin Lymphoma Nodular Regenerative Hyperplasia Non-a-E Hepatitis Nonalcoholic Steatohepatitis Non-Involuting Congenital Hemangioma Noonan Syndrome 1 Noonan Syndrome 2 Noonan Syndrome 3 Nutmeg Liver Obstructive Jaundice Occipital Horn Syndrome Ocular Albinism Ocular Melanoma Ocular Motor Apraxia Olecranon Bursitis Omphalocele Opiate Dependence Opisthorchiasis Opsoclonus-Myoclonus Syndrome Optic Nerve Hypoplasia, Bilateral Optic Neuritis Optic Perineuritis Oral Cavity Cancer Oral Erosive Lichen Oral Leukoplakia Oral Lichen Planus Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Orotic Aciduria Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrodysplasia Osteomalacia Osteomyelitis Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis Osteonecrosis Osteonecrosis of the Jaw Osteopetrosis Osteoporotic Fracture Ovarian Cancer Ovarian Hyperstimulation Syndrome Ovarian Serous Cystadenocarcinoma Overnutrition Paine Syndrome Palmoplantar Carcinoma, Multiple Self-Healing Pancreatic Acinar Cell Adenocarcinoma Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatic Endocrine Carcinoma Pancreatic Islet Cell Tumors Pancreatic Neuroendocrine Tumor Pancreatitis Pancytopenia Panniculitis Papillary Adenocarcinoma Papillary Adenoma Papillary Carcinoma Papillary Cystadenocarcinoma Papilloma Papillon-Lefevre Syndrome Paracetamol Poisoning Paracoccidioidomycosis Paraganglioma Paragangliomas 5 Paragonimiasis Paraneoplastic Pemphigus Paraplegia Paraquat Poisoning Parathyroid Carcinoma Paratyphoid Fever Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Parotitis Paroxysmal Nocturnal Hemoglobinuria Parsonage Turner Syndrome Pasteurella Multocida Infection Patent Ductus Venosus Pediatric Lymphoma Pediatric Multiple Sclerosis Peeling Skin Syndrome 1 Peliosis Hepatis Pelvic Inflammatory Disease Pemphigus Pemphigus Foliaceus Pemphigus Vulgaris Penicilliosis Pentalogy of Cantrell Pepck 1 Deficiency Peptic Ulcer Disease Pericardial Effusion Pericarditis Pericholangitis Perinephritis Periodontitis Periodontitis, Aggressive, 1 Periostitis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral T-Cell Lymphoma Peritoneal Mesothelioma Peritonitis Perivascular Epithelioid Cell Tumor Pernicious Anemia Peroxisome Disorders Persistent Idiopathic Facial Pain Pertussis Peutz-Jeghers Syndrome Pfeiffer Syndrome Pharyngitis Phelan-Mcdermid Syndrome Phenylketonuria Pheochromocytoma Phosphorylase Kinase Deficiency Photoparoxysmal Response 1 Photosensitive Epilepsy Pick Disease of Brain Pierre Robin Syndrome Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pitt-Hopkins Syndrome Pituitary Tumors Pityriasis Lichenoides Pityriasis Lichenoides Chronica Pityriasis Rosea Pityriasis Rubra Pilaris Placental Abruption Placental Insufficiency Plague Plantar Wart Plasmablastic Lymphoma Plasma Cell Leukemia Plasmacytoma Plasmodium Falciparum Malaria Plasmodium Vivax Malaria Pleomorphic Adenoma Pleomorphic Liposarcoma Pleurisy Pleuropneumonia Pleuropulmonary Blastoma Plexiform Neurofibroma Pneumatosis Cystoides Intestinalis Pneumocistoză Pneumococcal Meningitis Pneumonia Pneumonic Plague Pneumothorax Poliomyelitis Pollen Allergy Polyarteritis Nodosa Polyclonal Hypergammaglobulinemia Polycystic Echinococcosis Polycystic Kidney Disease Polycystic Kidney Disease 1 Polycystic Kidney Disease 4 with or Without Hepatic Disease Polycystic Kidney Disease 5 Polycystic Liver Disease Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polydactyly Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polymyositis Polyneuropathy Polyradiculoneuropathy Polysubstance Abuse Porokeratosis Porokeratosis 1, Multiple Types Porphyria Porphyria, Acute Hepatic Porphyria Cutanea Tarda Porphyria Cutanea Tarda, Type I Porphyria Variegata Portal Hypertension Portal Vein Thrombosis Postcholecystectomy Syndrome Posterior Urethral Valves Posttransplant Acute Limbic Encephalitis Post-Transplant Lymphoproliferative Disease Post-Traumatic Stress Disorder Postural Hypotension Potocki-Shaffer Syndrome Pouchitis Prader-Willi Syndrome Pre-Eclampsia Preeclampsia/eclampsia 1 Premature Ovarian Failure 7 Primary Agammaglobulinemia Primary Biliary Cholangitis Primary Biliary Cirrhosis Primary Central Nervous System Lymphoma Primary Cerebellar Degeneration Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Effusion Lymphoma Primary Hepatic Neuroendocrine Carcinoma Primary Hyperoxaluria Primary Hyperparathyroidism Proctitis Progressive Multifocal Leukoencephalopathy Progressive Myoclonus Epilepsy Proliferative Glomerulonephritis Prostate Cancer Prostatitis Protein C Deficiency Protein-Losing Enteropathy Prothrombin Deficiency Prune Belly Syndrome Prurigo Nodularis Pseudobulbar Affect Pseudocholinesterase Deficiency Pseudomyxoma Peritonei Psoriasis Psoriasis 13 Psoriatic Arthritis Psychotic Disorder Pulmonary Alveolar Microlithiasis Pulmonary Alveolar Proteinosis Pulmonary Alveolar Proteinosis, Acquired Pulmonary Arterio-Veinous Fistula Pulmonary Arteriovenous Fistulas Pulmonary Arteriovenous Malformation Pulmonary Edema Pulmonary Embolism Pulmonary Eosinophilia Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulmonary Sarcoidosis Pulmonary Tuberculosis Pure Red-Cell Aplasia Purpura Purpura Fulminans Pustular Psoriasis Pyelonephritis Pyoderma Pyoderma Gangrenosum Pyomyositis Pyridoxine Deficiency Pyruvate Carboxylase Deficiency Pyruvate Kinase Deficiency of Red Cells Pyuria Q Fever Radiculopathy Radin Blood Group Antigen Ramer Ladda Syndrome Rapidly Involuting Congenital Hemangioma Rapidly Progressive Glomerulonephritis Rapp-Hodgkin Syndrome Reactive Arthritis Recessive Dystrophic Epidermolysis Bullosa Rectosigmoid Junction Neoplasm Recurrent Acute Pancreatitis Recurrent Hypersomnia Reflex Sympathetic Dystrophy Refractory Anemia Refsum Disease, Classic Refsum Disease, Infantile Form Relapsing Polychondritis Renal Dysplasia Renal Glucosuria Renal-Hepatic-Pancreatic Dysplasia Renal Hypodysplasia/aplasia 1 Renal Tuberculosis Renal Tubular Acidosis Renpenning Syndrome 1 Restrictive Dermopathy, Lethal Reticular Dysgenesis Reticulosarcoma Reticulum Cell Sarcoma Retinal Artery Occlusion Retinal Degeneration Retinal Vasculitis Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Retinitis Pigmentosa and Erythrocytic Microcytosis Retinoblastoma Retinoschisis 1, X-Linked, Juvenile Retroperitoneal Fibrosis Retroperitoneal Liposarcoma Retroperitoneal Lymphoma Retroperitoneal Sarcoma Rett Syndrome Reversible Cerebral Vasoconstriction Syndrome Reye Syndrome Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rheumatic Disease Rheumatoid Arthritis Rheumatoid Nodulosis Rheumatoid Vasculitis Rhizomelic Chondrodysplasia Punctata Rhizomelic Chondrodysplasia Punctata, Type 3 Riboflavin Deficiency Rickettsialpox Rift Valley Fever Right Aortic Arch Ring Chromosome 2 Roberts Syndrome Rocky Mountain Spotted Fever Rosai-Dorfman Disease Rubella Salmonellosis Salpingitis Salt and Pepper Developmental Regression Syndrome Sandhoff Disease Sarcoidosis 2 Sarcoma Sarcosporidioză Satb2-Associated Syndrome Scalp-Ear-Nipple Syndrome Scarlet Fever Schistosomiasis Schizoaffective Disorder Schizophrenia Schnyder Corneal Dystrophy Scleritis Scleromyxedema Sclerosing Cholangitis Sclerosing Cholangitis, Neonatal Sclerosing Hemangioma Sclerosing Hepatic Carcinoma Scotoma Scott Syndrome Scrub Typhus Seckel Syndrome Secondary Syphilis Secretory Diarrhea Seizure Disorder Seizures, Benign Familial Neonatal, 1 Seizures, Scoliosis, and Macrocephaly Syndrome Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance Seminoma Sensorineural Hearing Loss Septic Arthritis Serotonin Syndrome Serous Cystadenocarcinoma Severe Acute Respiratory Syndrome Severe Combined Immunodeficiency Severe Congenital Neutropenia Severe Pre-Eclampsia Shaken Baby Syndrome Shigellosis Short Bowel Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Shwartzman Phenomenon Sialadenitis Sickle Beta Thalassemia Sickle Cell Anemia Sickle Cell Disease Sideroblastic Anemia Siderosis Silicosis Sitosterolemia Situs Inversus Sjogren Syndrome Skin Disease Skin Sarcoidosis Skin Tag Sleeping Sickness Small Cell Carcinoma Small Cell Neuroendocrine Carcinoma Smallpox Smith-Kingsmore Syndrome Smith-Lemli-Opitz Syndrome Smoldering Myeloma Smooth Muscle Tumor Somatostatinoma Sparganosis Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spastic Paraparesis Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spindle Cell Carcinoma Spindle Cell Hemangioma Spindle Cell Sarcoma Spinocerebellar Degeneration Spiradenoma Spleen Angiosarcoma Splenic Abscess Splenic Artery Aneurysm Splenic Diffuse Red Pulp Small B-Cell Lymphoma Splenic Disease Splenic Infarction Splenic Marginal Zone Lymphoma Splenic Sequestration Splenic Tuberculosis Splenomegaly Spondylarthropathy Spondyloarthropathy Spondylocarpotarsal Synostosis Syndrome Spondylocostal Dysostosis 5 Spondyloocular Syndrome Spotted Fever Squamous Cell Carcinoma Statin Toxicity Status Epilepticus Stiff-Person Syndrome Stomatitis Stormorken Syndrome Strongyloidiasis Sturge-Weber Syndrome Subacute Bacterial Endocarditis Subacute Cerebellar Degeneration Subacute Cutaneous Lupus Erythematosus Subacute Thyroiditis Substance Abuse Substance Dependence Sudden Arrhythmia Death Syndrome Sudden Cardiac Failure, Infantile Sudden Infant Death Syndrome Sudden Sensorineural Hearing Loss Superior Mesenteric Artery Syndrome Suppressor of Tumorigenicity 3 Suppurative Cholangitis Susac Syndrome Sveinsson Chorioretinal Atrophy Syncope Syndrome of Inappropriate Antidiuretic Hormone Synovitis Syphilis Systemic Lupus Erythematosus Systemic Mastocytosis Systemic Onset Juvenile Idiopathic Arthritis Systemic Polyarteritis Nodosa Taeniasis Tardive Dyskinesia Tarsal-Carpal Coalition Syndrome T Cell Deficiency T-Cell Leukemia Telangiectasis Temple-Baraitser Syndrome Temporal Arteritis Teratoma Tertiary Syphilis Testicular Cancer Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Testicular Seminoma Tetanus Tetralogy of Fallot Thalassemia Thoracoabdominal Syndrome Three M Syndrome 1 Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophlebitis Thrombophlebitis Migrans Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Thyroid Cancer Thyroid Cancer, Nonmedullary, 1 Thyroiditis Thyrotoxic Periodic Paralysis Tick-Borne Encephalitis Tick Paralysis Timothy Syndrome Tinea Capitis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tongue Cancer Tonsillitis Townes-Brocks Syndrome Toxic Megacolon Toxic Myocarditis Toxic Oil Syndrome Toxic Shock Syndrome Toxocariasis Toxoplasmoză Tracheal Cancer Transient Erythroblastopenia of Childhood Transitional Cell Carcinoma Transsexualism Transsexuality Transverse Myelitis Treacher Collins Syndrome 1 Trichinosis Trichohepatoenteric Syndrome 1 Tricuspid Valve Disease Tricuspid Valve Stenosis Triploidy Tropical Sprue Trypanosomiasis, Human East-African Tuberculoid Leprosy Tuberculous Meningitis Tuberculous Peritonitis Tuberous Sclerosis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Tularemia Tumefactive Multiple Sclerosis Turner Syndrome Type Ii Mixed Cryoglobulinemia Typhoidal Tularemia Typhoid Fever Tyrosinemia Tyrosinemia, Type I Tyrosinemia, Type Ii Tyrosinosis Ulcerative Colitis Ulceroglandular Tularemia Undifferentiated Connective Tissue Disease Undifferentiated Embryonal Sarcoma of the Liver Urate Oxidase, Pseudogene Urea Cycle Disorder Uremia Uremic Pruritus Ureteral Obstruction Urethritis Urinary Schistosomiasis Urticaria Uveitis Vaccinia Vaginitis Valproate Embryopathy Van Der Woude Syndrome 1 Varicocele Varicose Veins Vascular Disease Vasculitis Venezuelan Equine Encephalitis Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Vibrio Vulnificus Infection Villous Adenoma Vipoma Viral Encephalitis Viral Hepatitis Viral Infectious Disease Virus Associated Hemophagocytic Syndrome Virus-Associated Trichodysplasia Spinulosa Visceral Leishmaniasis Vitamin B12 Deficiency Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vogt-Koyanagi-Harada Disease Waldenstrom Macroglobulinemia Wandering Spleen Weber Syndrome West Nile Virus Whim Syndrome Wild Type Attr Amyloidosis Wilms Tumor 6 Wilson Disease Wiskott-Aldrich Syndrome Wolff-Parkinson-White Syndrome Wolf-Hirschhorn Syndrome Xanthogranulomatous Cholecystitis Xanthogranulomatous Pyelonephritis Xanthoma Disseminatum Xanthomatosis Xeroderma Pigmentosum, Variant Type X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome X-Linked Protoporphyria Yao Syndrome Yellow Fever Yellow Nail Syndrome Yemenite Deaf-Blind Hypopigmentation Syndrome Yunis-Varon Syndrome Zellweger Syndrome Zinc-Responsive Necrolytic Acral Erythema Zollinger-Ellison Syndrome Zygomycosis