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Boli A-Z 3-Beta-Hydroxysteroid Dehydrogenase Deficiency 3-Methylglutaconic Aciduria 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy 46,xy Sex Reversal 3 Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acanthamoeba Keratitis Acanthosis Nigricans Achalasia Acheiropody Achondrogenesis Achondrogenesis, Type Ii Achondroplasia Achromatopsia Acquired Cutis Laxa Acquired Immunodeficiency Syndrome Acral Lentiginous Melanoma Acrocallosal Syndrome Acromegaly Actinic Keratosis Actinic Prurigo Actinomycosis Acute Graft Versus Host Disease Acute Insulin Response Acute Leukemia Acute Liver Failure Acute Lymphocytic Leukemia Acute Myocardial Infarction Acute Pancreatitis Acute Promyelocytic Leukemia Acute Pyelonephritis Acute Respiratory Distress Syndrome Acute Salpingitis Acute Transverse Myelitis Adenocarcinoma Adenocarcinoma in Situ Adenohypophysitis Adenoiditis Adenoma Adenomyosis Adenosquamous Carcinoma Adrenal Adenoma Adrenal Carcinoma Adrenocortical Carcinoma, Hereditary Adrenoleukodystrophy Adrenomyeloneuropathy Adult Acute Lymphocytic Leukemia Adult Dermatomyositis Adult T-Cell Leukemia Afferent Loop Syndrome Afibrinogenemia Agammaglobulinemia Aganglionosis, Total Intestinal Aggressive Periodontitis Aging Agoraphobia Al Amyloidosis Aland Island Eye Disease Albinism Albinism, Oculocutaneous, Type Ii Alcohol Abuse Alcohol Dependence Alcoholic Cardiomyopathy Alcoholic Hepatitis Alcoholic Liver Cirrhosis Aldosterone-Producing Adenoma Alexander Disease Alk-Positive Anaplastic Large Cell Lymphoma Allergic Asthma Allergic Conjunctivitis Allergic Encephalomyelitis Allergic Rhinitis Alopecia Alopecia, Androgenetic, 1 Alopecia Areata 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 Alpha Chain Disease Alpha-Fetoprotein Deficiency Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Echinococcosis Alzheimer Disease 3 Amblyopia Amebiasis Amelanotic Melanoma Amenorrhea Amyloidosis Amyloidosis Beta2m Amyloidosis, Finnish Type Anal Canal Carcinoma Anaplastic Ependymoma Anaplastic Large Cell Lymphoma Anaplastic Oligoastrocytoma Anaplastic Oligodendroglioma Anauxetic Dysplasia 1 Ancylostomiasis Anemia, Congenital Dyserythropoietic, Type Ii Anencephaly Aneurysm Angelman Syndrome Angel-Shaped Phalangoepiphyseal Dysplasia Angioedema Angioimmunoblastic T-Cell Lymphoma Angiosarcoma Anhidrosis Aniridia 1 Aniseikonia Anismus Anisometropia Ankylosis Anorexia Nervosa 1 Anovulation Anterior Scleritis Anterior Segment Dysgenesis 2 Anthracycline Extravasation Antiphospholipid Syndrome Antisocial Personality Disorder Anuria Anus Disease Aortic Aneurysm Aortic Coarctation Aortic Valve Insufficiency Aortic Valve Prolapse Aortitis Aortopulmonary Window Aorto-Right Ventricular Tunnel Aphasia Aphthous Stomatitis Aplastic Anemia Apocrine Gland Secretion, Variation in Apolipoprotein C-Ii Deficiency Apolipoprotein C-Iii Deficiency Apparent Mineralocorticoid Excess Appendicitis Arachnoiditis Argyria Arteries, Anomalies of Arteriosclerosis Arteriosclerosis Obliterans Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthropathy Arthus Reaction Asbestos Intoxication Asbestosis Ascending Cholangitis Aspartylglucosaminuria Aspergillosis Aspirin Resistance Asthma Astigmatism Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Atelosteogenesis Atelosteogenesis, Type I Atelosteogenesis, Type Ii Atelosteogenesis, Type Iii Athetosis Atrial Fibrillation Atrichia with Papular Lesions Atrioventricular Block Atrophic Gastritis Atrophic Rhinitis Attention Deficit-Hyperactivity Disorder Audiogenic Seizures Aural Atresia, Congenital Autism Autoimmune Disease Autoimmune Encephalitis Autoimmune Hemolytic Anemia-Autoimmune Thrombocytopenia-Primary Immunodeficiency Syndrome Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Myocarditis Autoimmune Oophoritis Autoimmune Pancreatitis Autoimmune Polyendocrine Syndrome Autoimmune Polyendocrine Syndrome, Type Ii Autoimmune Retinopathy Autoinflammation with Infantile Enterocolitis Autonomic Neuropathy Autosomal Dominant Polycystic Kidney Disease Avian Influenza Azoospermia Babesiosis Bacterial Vaginosis Bagassosis Baraitser-Winter Syndrome 1 Bare Lymphocyte Syndrome, Type Ii Basal Cell Carcinoma B Cell Deficiency B-Cell Lymphomas Beckwith-Wiedemann Syndrome Bejel Beriberi Bernard-Soulier Syndrome Bestrophinopathy, Autosomal Recessive Beta-Adrenergic Stimulation, Response to Bifid Nose with or Without Anorectal and Renal Anomalies Bilateral Breast Cancer Biliary Atresia Biliary Tract Disease Bipolar Disorder Bipolar I Disorder Bk-Virus Nephropathy Bladder Cancer Blastoma Blastomycosis Bleeding Disorder, Platelet-Type, 11 Blepharitis Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group--Ul System Bloom 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 Cancer Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Boomerang Dysplasia Borderline Leprosy Borderline Personality Disorder Borna Disease Bornholm Eye Disease Bothnia Retinal Dystrophy Brachydactyly Brain Cancer Brain Glioma Brain Injury Brain Ischemia Brain Tumor, Childhood Branchial Cleft Anomalies Breast Adenocarcinoma Breast Cancer Breast Disease Brittle Bone Disorder Broken Heart Syndrome Bronchiectasis Bronchopneumonia Brooke-Spiegler Syndrome Budd-Chiari Syndrome Bullous Pemphigoid Burkitt Lymphoma Burns Burn Scar Bursitis Buruli Ulcer Byssinosis Candidiasis Cardiac Arrest Cardiac Conduction Defect Cardiac Rupture Cardiogenic Shock Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cardiovascular Syphilis Carnitine Palmitoyltransferase Ii Deficiency, Infantile Carotid Artery Occlusion Carotid Stenosis Carpal Tunnel Syndrome Carpenter Syndrome 1 Cartilage Disease Cartilage-Hair Hypoplasia Cataract Cataract 13 with Adult I Phenotype Cataract 40 Cataract 5, Multiple Types Cataract Congenital Dominant Non Nuclear Cataract, Total Congenital Cat-Scratch Disease Causalgia Cellulitis Central Nervous System Disease Central Nervous System Lymphoma Central Nervous System Origin Vertigo Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Sleep Apnea Cerebellar Degeneration Cerebellar Degeneration-Related Autoantigen 3 Cerebellar Hypoplasia Cerebral Amyloid Angiopathy, App-Related Cerebral Aneurysms Cerebral Artery Occlusion Cerebral Atherosclerosis Cerebral Cavernous Malformations Cerebral Hemorrhage Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cerebro-Oculo-Facio-Skeletal Syndrome Cerebrovascular Disease Cervical Adenocarcinoma Cervical Cancer Cervical Intraepithelial Neoplasia Cervical Squamous Cell Carcinoma Cervicitis Cervix Carcinoma Charles Bonnet Syndrome Chediak-Higashi Syndrome Cheilitis Cherubism Chiari Malformation Chiari Malformation Type I Chiari Malformation Type Ii Chikungunya Childhood Absence Epilepsy Childhood Leukemia Childhood Medulloblastoma Chlamydia Choanal Atresia, Posterior Cholangiocarcinoma Cholangitis Cholecystitis Choledocholithiasis Cholera Cholestasis Cholestasis-Lymphedema Syndrome Chondroblastic Osteosarcoma Chondroblastoma Chondromyxoid Fibroma Chondrosarcoma Chops Syndrome Chordoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Choriocarcinoma Chorioretinitis Choroiditis Chromoblastomycosis Chromophil Adenoma of the Kidney Chromosomal Triplication Chronic Enteropathy Associated with Slco2a1 Gene Chronic Fatigue Syndrome Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Myelomonocytic Leukemia Chronic Pain Chronic Recurrent Multifocal Osteomyelitis Chronic Thromboembolic Pulmonary Hypertension Chronic Ulcer of Skin Chylomicron Retention Disease Citrullinemia, Classic Citrullinemia, Type Ii, Adult-Onset Citrullinemia, Type Ii, Neonatal-Onset Clear Cell Renal Cell Carcinoma Cleft Larynx, Posterior Cleft Lip Cloacal Exstrophy Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Cocaine Abuse Cocaine Dependence Coccidioidomycosis Cockayne Syndrome Cockayne Syndrome B Cockayne Syndrome Type Ii Coffin-Lowry Syndrome Cogan-Reese Syndrome Cognitive Impairment with or Without Cerebellar Ataxia Colitis Collagen Disease Collagenopathy Type 2 Alpha 1 Colon Adenocarcinoma Colon Adenoma Colorado Tick Fever Colorblindness, Partial, Protan Series Colorectal Adenocarcinoma Colorectal Adenoma Colorectal Cancer Common Variable Immunodeficiency Complement Component 2 Deficiency Complement Component 3 Deficiency Complement Factor B Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Conduct Disorder Congenital Bile Acid Synthesis Defect Congenital Cytomegalovirus Congenital Dislocation of the Patella Congenital Disorder of Glycosylation, Type Ii Congenital Disorder of Glycosylation, Type Iic Congenital Disorders of N-Linked Glycosylation and Multiple Pathway Congenital Dyserythropoietic Anemia Congenital Extrahepatic Portosystemic Shunt Congenital Fiber-Type Disproportion Congenital Generalized Lipodystrophy Congenital Herpes Simplex Congenital Ichthyosiform Erythroderma Congenital Methemoglobinemia Congenital Nystagmus Congenital Short Bowel Syndrome Congenital Syphilis Congenital Toxoplasmosis Congestive Heart Failure Conjunctival Folliculosis Conjunctivitis Conotruncal Heart Malformations Constipation Constricting Bands, Congenital Contagious Pustular Dermatitis Corneal Disease Corneal Dystrophy Corneal Dystrophy, Avellino Type Corneal Edema Corneal Granular Dystrophy Corneal Neovascularization Coronary Artery Anomaly Coronary Stenosis Coronary Thrombosis Corticosteroid-Binding Globulin Deficiency Corticosterone Methyloxidase Type Ii Deficiency Cortisone Reductase Deficiency 1 Costello Syndrome Cowpox Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniopharyngioma Craniosynostosis Craniosynostosis 2 Crescentic Glomerulonephritis Crigler-Najjar Syndrome, Type Ii Critical Limb Ischemia Crohn's Colitis Crohn's Disease Cryoglobulinemia Cutaneous Leishmaniasis Cutaneous Lupus Erythematosus Cutaneous T Cell Lymphoma Cutis Laxa Cutis Verticis Gyrata Cyclic Neutropenia Cycloplegia Cystadenocarcinoma Cysticercosis Cystic Fibrosis Cystinuria Cystitis Cytomegalovirus Infection D-2-Hydroxyglutaric Aciduria 1 Dandy-Walker Syndrome Decubitus Ulcer Dedifferentiated Liposarcoma Degenerative Disc Disease Dementia Demodicidosis Dengue Hemorrhagic Fever Dengue Virus Dense Deposit Disease Dense Deposit Disease/membranoproliferative Glomerulonephritis Type Ii Dentin Dysplasia Dentin Dysplasia, Type Ii Dentinogenesis Imperfecta Denture Stomatitis Dermatitis Dermatitis Herpetiformis Dermatomycosis Dermatomyositis Dermatophytosis Desmoid Disease, Hereditary Desmoplastic Small Round Cell Tumor Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Diabetes Mellitus, Noninsulin-Dependent Diabetic Foot Ulcers Diabetic Macular Edema Diabetic Mastopathy Diabetic Neuropathy Diabetic Polyneuropathy Diaphanospondylodysostosis Diastematomyelia Diastolic Heart Failure Dicrocoeliasis Differentiated Thyroid Carcinoma Diffuse Intrinsic Pontine Glioma Diffuse Large B-Cell Lymphoma Diffuse Lymphatic Malformation Digeorge Syndrome Dihydrolipoamide Dehydrogenase Deficiency Dilated Cardiomyopathy Diphtheria Discitis Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Distal Arthrogryposis Distal Hereditary Motor Neuropathies Distal Hereditary Motor Neuropathy, Type Ii Distal Trisomy 14q Donnai-Barrow Syndrome Down Syndrome Drug Dependence Drug-Induced Lupus Erythematosus Duane Retraction Syndrome 1 Dubin-Johnson Syndrome Dubowitz Syndrome Dumping Syndrome Duodenal Ulcer Duodenitis Dwarfism Dysautonomia Dyschromatosis Symmetrica Hereditaria Dysentery Dysfibrinogenemia Dyskeratosis Congenita Dysostosis Dyspepsia Dysphagia Dystonia Eastern Equine Encephalitis Eating Disorder Echinococcosis Eclampsia Ecthyma Ectodermal Dysplasia Egg Allergy Ehlers-Danlos Syndrome Encephalitis Encephalocele Encephalomalacia Encephalomyopathy Encephalopathy Endemic Goiter Endocrine Exophthalmos Endogenous Depression Endometrial Adenocarcinoma Endometrial Cancer Endometriosis Endometriosis of Ovary Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Enophthalmos Enterocolitis Enteropathy-Associated T-Cell Lymphoma Ependymoma Epiblepharon Epidemic Pleurodynia Epidemic Typhus Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epidermolysis Bullosa Pruriginosa Epidermolytic Hyperkeratosis Epilepsy Epilepsy, Pyridoxine-Dependent Episodic Ataxia Epispadias Epithelial Recurrent Erosion Dystrophy Epithelioid Hemangioendothelioma Erysipelas Erythema Multiforme Esophageal Cancer Essential Iris Atrophy Essential Thrombocythemia Esterase C Estrogen-Receptor Positive Breast Cancer Ewing Sarcoma Exertional Headache Exocrine Pancreatic Insufficiency Exophthalmos Exostoses, Multiple, Type I Exostosis Extra-Adrenal Pheochromocytoma Extraocular Retinoblastoma Fabry Disease Facial Paralysis Facioscapulohumeral Muscular Dystrophy 1 Factor Vii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Familial Adenomatous Polyposis Familial Amyloidosis, Finnish Type Familial Hyperaldosteronism Familial Hypertension Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fanconi Syndrome Fasciitis Fascioliasis Fasting Hypoglycemia Fatty Liver Disease Febrile Seizures Feingold Syndrome 1 Fetal Iodine Deficiency Disorder Fibrodysplasia Ossificans Progressiva Fibromatosis Fibrous Histiocytoma Fibular Hemimelia Fibular Hypoplasia and Complex Brachydactyly First Branchial Cleft Anomaly Fish-Eye Disease Floating-Harbor Syndrome Focal Cortical Dysplasia, Type Ii Focal Epilepsy Follicular Lymphoma Fontaine Progeroid Syndrome Food Allergy Friedreich Ataxia 1 Frontometaphyseal Dysplasia 1 Frontotemporal Dementia Frontotemporal Dementia, Chromosome 3-Linked Fucosidase Regulator Fucosidosis Fundus Albipunctatus Galactose Epimerase Deficiency Galactosemia Gallbladder Cancer Gallbladder Disease Gangliosidosis Gm2 Gastric Adenocarcinoma Gastric Cancer Gastric Cardia Adenocarcinoma Gastric Lymphoma Gastric Ulcer Gastrinoma Gastritis Gastroduodenitis Gastroenteritis Gastroesophageal Junction Adenocarcinoma Gastroesophageal Reflux Gastrointestinal Stromal Tumor Gastrojejunal Ulcer Genitopatellar Syndrome Germ Cells Tumors Gestational Diabetes Giant Cell Myocarditis Giant Cell Tumor Giant Papillary Conjunctivitis Gilles De La Tourette Syndrome Gillessen-Kaesbach-Nishimura Syndrome Gingival Recession Gingivitis Glanders Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glossopharyngeal Neuralgia Glucose/galactose Malabsorption Glucose Transporter Type 1 Deficiency Syndrome Glycogen Storage Disease Glycogen Storage Disease Ii Glycogen Storage Disease Ixa1 Glycogen Storage Disease V Glycoproteinosis Gm1-Gangliosidosis, Type Ii Goiter Gonadal Dysgenesis Gonadoblastoma Gout Grade Iii Astrocytoma Graft-Versus-Host Disease Granulocytopenia Granuloma Inguinale Granulomatous Amebic Encephalitis Graves' Disease Greig Cephalopolysyndactyly Syndrome Griscelli Syndrome Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Guillain-Barre Syndrome, Familial Gyrate Atrophy of Choroid and Retina Haemophilus Influenzae Hair Disease Hairy Cell Leukemia Hairy Nose Tip Hajdu-Cheney Syndrome Hanhart Syndrome Hansen's Disease Headache Headache Associated with Sexual Activity Head Injury Heavy Metal Poisoning Helicobacter Pylori Infection Helix Syndrome Hellp Syndrome Hemangioendothelioma Hemangioma Hemangiopericytoma, Malignant Hematopoietic Stem Cell Transplantation Heme Oxygenase 1 Deficiency Hemicrania Continua Hemifacial Atrophy, Progressive Hemifacial Spasm Hemiplegia Hemochromatosis, Neonatal Hemochromatosis, Type 1 Hemoglobinuria Hemolytic-Uremic Syndrome Hemopericardium Hemophagocytic Lymphohistiocytosis Hemophilia Hemophilia B Hemophilic Arthropathy Hemorrhagic Fever Heparin Cofactor Ii Deficiency Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Coma Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis D Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hepatopulmonary Syndrome Hereditary Angioedema Hereditary Antithrombin Deficiency Hereditary Neuropathies Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Sensory Neuropathy Hereditary Spherocytosis Hereditary Wilms' Tumor Hereditary Xanthinuria Hermansky-Pudlak Syndrome Heroin Dependence Herpes Simplex Herpes Zoster Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Histiocytoma Histiocytosis Histiocytosis-Lymphadenopathy Plus Syndrome Histoplasmosis Holoprosencephaly Horns in Sheep Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Huntington Disease-Like 3 Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydromyelia Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type Ii Hyperalphalipoproteinemia 1 Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hyperglycemia Hyperinsulinism Hyperlipoproteinemia, Type V Hyperoxaluria, Primary, Type Ii Hyperparathyroidism Hyperproinsulinemia Hyperprolinemia Hypertelorism Hypertension, Diastolic Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertension, Essential Hypertensive Encephalopathy Hypertensive Heart Disease Hyperthyroidism Hypertonia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Scars Hypervitaminosis a Hypoactive Sexual Desire Disorder Hypoadrenalism Hypoaldosteronism Hypoascorbemia Hypocalcemia, Autosomal Dominant 1 Hypochondrogenesis Hypoglycemia Hypoglycemic Coma Hypoparathyroidism Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypoplastic Left Heart Syndrome Hypospadias Hypotonia-Cystinuria Syndrome Hypoxia Ichthyosis Prematurity Syndrome Idiopathic Hemiconvulsion-Hemiplegia Syndrome Idiopathic Infantile Hypercalcemia Immune-Complex Glomerulonephritis Immune Deficiency Disease Immune Suppression Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Impetigo Impotence Inclusion Body Myositis Inclusion Conjunctivitis Incontinentia Pigmenti Indolent B Cell Lymphoma Infective Dermatitis Associated with Htlv-1 Infertility Influenza in Situ Carcinoma Insulin-Like Growth Factor I Insulinoma Intellectual Disability-Developmental Delay-Contractures Syndrome Intermittent Claudication Interstitial Cystitis Interstitial Keratitis Interstitial Lung Disease Intestinal Benign Neoplasm Intestinal Disease Intestinal Perforation Intestinal Tuberculosis Intracranial Aneurysm Intracranial Hypertension Intrahepatic Cholangiocarcinoma Intrahepatic Cholestasis Intraocular Retinoblastoma Intrauterine Infections Invasive Aspergillosis Invasive Bladder Transitional Cell Carcinoma Inverted Follicular Keratosis Iridocyclitis Irritable Bowel Syndrome Ischemia Ischiocoxopodopatellar Syndrome Islet Cell Tumor Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Ia Isolated Growth Hormone Deficiency, Type Ii Isolated Optic Neuritis Isovaleric Acidemia Japanese Encephalitis Joint Disorders Juvenile Nasopharyngeal Angiofibroma Kaposi Sarcoma Kashin-Beck Disease Kawasaki Disease Kearns-Sayre Syndrome Keloids Keratinizing Squamous Cell Carcinoma Keratitis, Hereditary Keratoconjunctivitis Keratoconjunctivitis Sicca Keratoconus Keratomalacia Keratosis Kernicterus Kidney Cancer Kidney Hypertrophy Klatskin's Tumor Kleeblattschaedel Kniest Dysplasia Kwashiorkor Kyasanur Forest Disease Lactic Acidosis Lactose Intolerance Lambdoid Synostosis Lambert-Eaton Myasthenic Syndrome Large Cell Carcinoma Large Cell Neuroendocrine Carcinoma Laryngeal Cleft Laryngitis Laryngotracheitis Lassa Fever Lateral Sclerosis Lathyrism Lattice Corneal Dystrophy Lattice Corneal Dystrophy Type Ii Laugier-Hunziker Syndrome Leber Congenital Amaurosis Leber Congenital Amaurosis 5 Lecithin:cholesterol Acyltransferase Deficiency Leigh Syndrome Leiomyoma Leiomyomatosis Leiomyosarcoma Leishmaniasis Lentigines Lepromatous Leprosy Leptin Receptor Deficiency Leukemia Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukoplakia Leydig Cell Hypoplasia Lichen Planus Limb-Body Wall Complex Limb Ischemia Linear Porokeratosis Lipid Pneumonia Lipodystrophy Lipodystrophy, Partial, Acquired Lipoid Nephrosis Liposarcoma Lissencephaly Lissencephaly 1 Lissencephaly 2 Livedoid Vasculopathy Liver Cirrhosis Liver Disease Localized Osteosarcoma Loeys-Dietz Syndrome Loeys-Dietz Syndrome 3 Logopenic Progressive Aphasia Loiasis Long Qt Syndrome Louping Ill Louse-Borne Relapsing Fever Lung Cancer Lung Cancer Susceptibility 1 Lung Disease Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome Lung Squamous Cell Carcinoma Lupus Erythematosus Lyme Disease Lymphangioleiomyomatosis Lymphangitis Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphocytic Choriomeningitis Lymphogranuloma Venereum Lymphoid Leukemia Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphoma, Non-Hodgkin, Familial Lymphomatoid Papulosis Lymphopenia Lymphoproliferative Syndrome Lymphosarcoma Lynch Syndrome Lynch Syndrome I Lysosomal Storage Disease Macrocytic Anemia Macroglobulinemia Macs Syndrome Macular Dystrophy, Corneal Macular Holes Madelung Deformity Major Affective Disorder 8 Major Affective Disorder 9 Malaria Malignant Glioma Malignant Hypertension Malignant Peritoneal Mesothelioma Malignant Pleural Mesothelioma Mannosidosis Mantle Cell Lymphoma Marasmus Marfan Syndrome Marginal Zone B-Cell Lymphoma Marshall Syndrome Mastitis Mature Teratoma Maturity-Onset Diabetes of the Young Mayer-Rokitansky-Kuster-Hauser Syndrome Mckusick-Kaufman Syndrome Measles Mediastinitis Medulloblastoma Megaloblastic Anemia Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency Melancholia Melanoma Melnick-Needles Syndrome Melorheostosis, Isolated Membranoproliferative Glomerulonephritis Membranous Nephropathy Meninges Hemangiopericytoma Meningioma, Familial Meningitis Meningococcal Infection Meningococcal Meningitis Meningococcemia Meningoencephalitis Meningoencephalocele Menkes Disease Mercury Poisoning Merkel Cell Carcinoma Metabolic Acidosis Metachromatic Leukodystrophy Methemoglobinemia Methemoglobinemia, Beta-Globin Type Mevalonic Aciduria Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii Microcephaly Microcephaly 1, Primary, Autosomal Recessive Microcephaly, Epilepsy, and Diabetes Syndrome Microcytic Anemia Microtia Migraine with or Without Aura 1 Miller Fisher Syndrome Mirizzi Syndrome Mitochondrial Complex Ii Deficiency Mitochondrial Myopathy Mixed Malaria Miyoshi Muscular Dystrophy 1 Mobitz Type Ii Atrioventricular Block Mohr Syndrome Mohr-Tranebjaerg Syndrome Mongolian Spot Monilethrix Monkeypox Monocytic Leukemia Mononeuropathy Mononeuropathy of the Median Nerve, Mild Mood Disorder Morbid Obesity Morphine Dependence Mosaic Trisomy 5 Motion Sickness Motor Neuron Disease Mouth Disease Moyamoya Disease 1 Mu Chain Disease Mucinous Adenocarcinoma Mucolipidoses Mucolipidosis Ii Alpha/beta Mucolipidosis Iii Alpha/beta Mucolipidosis Iv Mucopolysaccharidoses Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis, Type Iiib Mucopolysaccharidosis Type Vi Mucopolysaccharidosis, Type Vii Mucositis Muir-Torre Syndrome Mulchandani-Bhoj-Conlin Syndrome Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies Multicentric Reticulohistiocytosis Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Pterygium Syndrome, Lethal Type Multiple Sclerosis Multiple Self-Healing Squamous Epithelioma Multiple Sulfatase Deficiency Multiple System Atrophy 1 Mumps Mungan Syndrome Murray Valley Encephalitis Muscle Hypertrophy Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Congenital Merosin-Deficient, 1a Musical Perfect Pitch Mutagen Sensitivity Mutism Myasthenia Gravis Mycetoma Mycoplasmal Pneumonia Mycosis Fungoides Myd88 Deficiency Myelitis Myelocystocele Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myelomeningocele Myocardial Infarction Myocardial Stunning Myocarditis Myoclonic Astatic Epilepsy Myoclonic Epilepsy of Lafora Myoclonus Myofibrillar Myopathy Myoglobinuria Myoglobinuria, Acute Recurrent, Autosomal Recessive Myoma Myopathy Myopia Myositis Myotonic Dystrophy Myxedema N-Acetylaspartate Deficiency Narcolepsy Nasopharyngeal Carcinoma Nasopharyngitis Navicular Bone, Accessory Necrobiosis Lipoidica Necrotizing Fasciitis Necrotizing Ulcerative Gingivitis Nemaline Myopathy Neonatal Lupus Erythematosus Neonatal Stroke Neovascular Glaucoma Nephrocalcinosis Nephrosclerosis Nephrotic Syndrome Nerve Compression Syndrome Nervous System Cancer Nervous System Disease Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neuraminidase Deficiency Neuritis Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Carcinoma of the Cervix Neuroendocrine Tumor Neurofibromatosis, Type Ii Neurofibromatosis, Type Iv, of Riccardi Neurogenic Bladder Neurogenic Hypertension Neuroleptic Malignant Syndrome Neuromuscular Disease Neuromyelitis Optica Neuronal Migration Disorders Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iia Neutropenia Neutrophil Actin Dysfunction Nevus Comedonicus Newcastle Disease Nodular Basal Cell Carcinoma Nonalcoholic Steatohepatitis Nonseminomatous Germ Cell Tumor Nontuberculous Mycobacterial Lung Disease Noonan Syndrome 1 Noonan Syndrome 3 Noonan Syndrome 5 Obstructive Jaundice Occipital Encephalocele Occipital Horn Syndrome Ocular Albinism Ocular Hypertension Ocular Melanoma Ocular Motor Apraxia Ocular Toxoplasmosis Oculocutaneous Albinism Oligoastrocytoma Oligodendroglioma Oligospermia Omenn Syndrome Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex Oncogenic Osteomalacia Opisthorchiasis Opitz Gbbb Syndrome, Type I Opitz Gbbb Syndrome, Type Ii Opitz-Kaveggia Syndrome Oppositional Defiant Disorder Optic Neuritis Oral Candidiasis Oral Leukoplakia Oral Squamous Cell Carcinoma Oral Submucous Fibrosis Orbital Disease Orbital Melanoma Ornithosis Orofaciodigital Syndrome Orofaciodigital Syndrome Vi Orotic Aciduria Orthostatic Proteinuria Osgood-Schlatter's Disease Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteoblastoma Osteochondrodysplasia Osteochondrosis Osteofibrous Dysplasia Osteogenesis Imperfecta, Type Ii Osteogenic Sarcoma Osteomalacia Osteomyelitis Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis Osteonecrosis Osteonecrosis of the Jaw Osteopetrosis Osteopetrosis, Autosomal Recessive 3 Osteoporotic Fracture Ostertagiasis Otitis Externa Otitis Media Otomycosis Oto-Palatal-Digital Syndrome Otopalatodigital Syndrome Otopalatodigital Syndrome, Type Ii Otosclerosis Ovarian Cancer Ovarian Cancer 1 Ovarian Clear Cell Carcinoma Ovarian Cyst Ovarian Disease Ovarian Epithelial Cancer Ovarian Hyperstimulation Syndrome Overhydrated Hereditary Stomatocytosis Overnutrition Pachygyria Pacman Dysplasia Paine Syndrome Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatic Endocrine Carcinoma Pancreatic Gastrinoma Pancreatic Islet Cell Tumors Pancreatitis Pancreatitis, Hereditary Pancytopenia Panic Disorder Papillary Adenoma Papillary Conjunctivitis Papillary Ependymoma Papilledema Papilloma Papillomatosis, Confluent and Reticulated Paracoccidioidomycosis Paraganglioma Paragonimiasis Paralytic Ileus Paralytic Poliomyelitis Paraneoplastic Pemphigus Paraquat Poisoning Parkinson Disease 15, Autosomal Recessive Early-Onset Parotitis Paroxysmal Nocturnal Hemoglobinuria Pars Planitis Partial Deletion of Y Pasteurella Multocida Infection Patent Ductus Venosus Pdgfrb-Associated Chronic Eosinophilic Leukemia Peanut Allergy Pediatric Osteosarcoma Pelizaeus-Merzbacher Disease Pemphigoid Gestationis Pemphigus Pemphigus Erythematosus Pemphigus Foliaceus Pemphigus Vulgaris Penile Cancer Penile Cancer, Adult Pentalogy of Cantrell Peptic Ulcer Disease Pericarditis Pericoronitis Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis Periodontal Disease Periodontal Ehlers-Danlos Syndrome Periodontitis Peripartum Cardiomyopathy Peripheral Artery Disease Peripheral T-Cell Lymphoma Peritoneal Mesothelioma Peritoneum Cancer Peritonitis Periventricular Nodular Heterotopia Pernicious Anemia Persistent Idiopathic Facial Pain Persistent Mullerian Duct Syndrome Personality Disorder Pertussis Phacomatosis Pigmentovascularis Phaeochromocytoma Phaeohyphomycosis Pheochromocytoma Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked Pineoblastoma Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pituitary Stalk Interruption Syndrome Pituitary Tumors Pityriasis Rubra Pilaris Pityriasis Versicolor Plagiocephaly Plasmablastic Lymphoma Plasma Cell Leukemia Plasmacytoma Plasmodium Falciparum Malaria Platelet Disorder, Familial, with Associated Myeloid Malignancy Platelet Glycoprotein Iv Deficiency Platelet Membrane Fluidity Pleomorphic Adenoma Pleural Disease Pleurisy Pleuropneumonia Pleuropulmonary Blastoma Pneumoconiosis Pneumonia Pneumothorax Pneumothorax, Primary Spontaneous Poems Syndrome Poliomyelitis Polycystic Kidney Disease Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polydactyly Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polymorphic Reticulosis Polymyositis Polyneuropathy Porokeratosis Porphyria Porphyria Variegata Portal Hypertension Portal Vein Thrombosis Postpartum Depression Post-Traumatic Stress Disorder Pre-Eclampsia Pregnancy Loss, Recurrent 1 Premature Chromatid Separation Trait Premature Ejaculation Premature Ovarian Failure 7 Premenstrual Tension Presbyopia Priapism Prieto X-Linked Mental Retardation Syndrome Primary Biliary Cirrhosis Primary Central Nervous System Lymphoma Primary Congenital Glaucoma Primary Hyperoxaluria Primary Mediastinal Large B-Cell Lymphoma Primary Optic Atrophy Primary Peritoneal Carcinoma Primary Pigmented Nodular Adrenocortical Disease Primary Syphilis Progesterone-Receptor Positive Breast Cancer Prolidase Deficiency Proliferative Glomerulonephritis Prolymphocytic Leukemia Prostate Cancer Prostatic Adenoma Prostatic Hyperplasia, Benign Prostatitis Protein C Deficiency Protein S Deficiency Proximal Spinal Muscular Atrophy Pseudoachondroplasia Pseudobulbar Affect Pseudohermaphroditism Pseudohypoaldosteronism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ii Pseudomyxoma Peritonei Psoriasis Psoriasis 13 Psoriasis 2 Psoriasis 7 Psoriatic Arthritis Pulmonary Alveolar Proteinosis Pulmonary Arteriovenous Malformation Pulmonary Disease, Chronic Obstructive Pulmonary Embolism Pulmonary Eosinophilia Pulmonary Fibrosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonary Hypertension, Primary, 3 Pulmonary Sarcoidosis Pulmonary Sclerosing Hemangioma Pulmonary Sequestration Pulmonary Tuberculosis Pulpitis Pulsating Exophthalmos Purpura Purpura Fulminans Pustulosis Palmaris Et Plantaris Pyelonephritis Pyridoxine Deficiency Pyruvate Kinase Deficiency of Red Cells Q Fever Quadriplegia Rabies Ramer Ladda Syndrome Rapidly Progressive Glomerulonephritis Rapp-Hodgkin Syndrome Rasmussen Encephalitis Reading Disorder Recessive Dystrophic Epidermolysis Bullosa Rectal Disease Recurrent Respiratory Papillomatosis Reflex Sympathetic Dystrophy Refractory Anemia Refractory Anemia with Excess Blasts Refsum Disease, Classic Relapsed/refractory Diffuse Large B-Cell Lymphoma Relapsing Fever Relapsing Polychondritis Relapsing-Remitting Multiple Sclerosis Renal Fibrosis Renal Glucosuria Renal Hypertension Renal Tuberculosis Renal Tubular Acidosis Renoprival Hypertension Renovascular Hypertension Restrictive Cardiomyopathy Reticulosarcoma Retinal Artery Occlusion Retinal Degeneration Retinal Detachment Retinal Ischemia Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Retinoblastoma Retroperitoneal Sarcoma Rhabdomyosarcoma Rheumatic Disease Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatic Heart Disease Rheumatoid Arthritis Rhinitis Rhinosporidiosis Rhombencephalosynapsis Riboflavin Transporter Deficiency Richter's Syndrome Rickets Right Aortic Arch Right Bundle Branch Block Ring Chromosome 18 Roberts Syndrome Rocky Mountain Spotted Fever Root Resorption Rosacea Rubella Rubeosis Iridis Sacral Defect with Anterior Meningocele Saethre-Chotzen Syndrome Salivary Gland Adenoma, Pleomorphic Salmonellosis Salpingitis Salt and Pepper Developmental Regression Syndrome Sandhoff Disease Sarcoidosis 2 Sarcoma Sarcomatosis Sarcosinemia Scabies Scar Contracture Scarlet Fever Schistosomiasis Schizencephaly Schizoaffective Disorder Schizophrenia Schizotypal Personality Disorder Schnyder Corneal Dystrophy Sciatic Neuropathy Scleritis Sclerosing Cholangitis Sclerosing Cholangitis, Neonatal Sclerosing Hemangioma Scoliosis Scotoma Scott Syndrome Scrapie Sebastian Syndrome Seckel Syndrome Second-Degree Atrioventricular Block Semantic Dementia Seminoma Sensorineural Hearing Loss Serous Cystadenocarcinoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Sezary's Disease Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Short-Rib Thoracic Dysplasia 6 with or Without Polydactyly Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwartzman Phenomenon Sialadenitis Sickle Cell Anemia Sickle Cell Disease Sick Sinus Syndrome Siderosis Silent Myocardial Infarction Silicosis Silver-Russell Syndrome Sinusitis Skeletal Dysplasias Skin Benign Neoplasm Skin Disease Skin Melanoma Sleep Apnea Sleep Disorder Sleeping Sickness Slipped Capital Femoral Epiphysis Small Cell Cancer of the Lung Small Cell Carcinoma Small Cell Neuroendocrine Carcinoma Smallpox Smith-Kingsmore Syndrome Smith-Lemli-Opitz Syndrome Smooth Muscle Tumor Soft Tissue Sarcoma Solar Urticaria Space Motion Sickness Spasmodic Dysphonia Spastic Cerebral Palsy Spasticity Spastic Paraparesis Spermatogenic Failure 6 Spina Bifida Aperta Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy, Type I Spinal Muscular Atrophy, Type Ii Spinal Shock Spinocerebellar Ataxia 29 Splenomegaly Split Spinal Cord Malformation Spondylitis Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Spondyloenchondrodysplasia Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondyloepiphyseal Dysplasia Congenita Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondylolisthesis Spondyloocular Syndrome Spondyloperipheral Dysplasia Spondylosis Sporadic Breast Cancer Sporotrichosis Spotted Fever Squamous Cell Carcinoma Squamous Cell Carcinoma of the Larynx Stachybotrys Chartarum Status Asthmaticus Status Epilepticus Steatorrhea Stereotypic Movement Disorder Stickler Syndrome Stickler Syndrome, Type Ii Stiff-Person Syndrome St. Louis Encephalitis Stomatitis Strabismus Streptococcal Meningitis Strongyloidiasis Sturge-Weber Syndrome Subclavian Artery Aneurysm Subcortical Arteriosclerotic Encephalopathy Substance Abuse Subvalvular Aortic Stenosis Superficial Basal Cell Carcinoma Superficial Keratitis Suppressor of Tumorigenicity 3 Suppurative Otitis Media Sveinsson Chorioretinal Atrophy Swayback Synchronous Bilateral Breast Carcinoma Syndrome of Inappropriate Antidiuretic Hormone Synesthesia Synostosis Synovial Chondromatosis Synovitis Synpolydactyly Synpolydactyly 1 Synpolydactyly 2 Syphilis Syringomyelia Systemic Lupus Erythematosus Systemic Mastocytosis Systolic Heart Failure Taeniasis Tafro Syndrome Talipes Equinovarus Tangier Disease Tarp Syndrome Tay-Sachs Disease T-Cell Leukemia T-Cell Prolymphocytic Leukemia Telecanthus Telogen Effluvium Temperature Sensitivity Complementation, Cell Cycle Specific, Ts13 Temporal Lobe Epilepsy Tendinitis Tendinopathy Teratocarcinoma Teratoma Testicular Cancer Testicular Seminoma Testicular Torsion Tetanus Thalassemia Thanatophoric Dysplasia, Type I Thanatophoric Dysplasia, Type Ii Theileriasis Third-Degree Atrioventricular Block Thoracoabdominal Syndrome Three M Syndrome 1 Thrombasthenia Thrombocytopenia Thrombophilia Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thymic Epithelial Tumor Thymoma Thyroid Cancer Thyroiditis Thyrotoxic Periodic Paralysis Tic Disorder Tick-Borne Encephalitis Tick Infestation Timothy Syndrome Tinea Imbricata Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tongue Cancer Tongue Squamous Cell Carcinoma Tonsillitis Tooth Agenesis Tooth Ankylosis Tooth Resorption Toxic Maculopathy Toxic Shock Syndrome Toxoplasmoză Trachoma Transcobalamin I Deficiency Transcobalamin Ii Deficiency Transient Cerebral Ischemia Transitional Cell Carcinoma Transsexualism Transsexuality Transverse Myelitis Traumatic Brain Injury Tremor Trench Fever Trichinosis Trichorhinophalangeal Syndrome Trichorhinophalangeal Syndrome, Type Ii Trichothiodystrophy 4, Nonphotosensitive Trichotillomania Trichuriasis Tricuspid Atresia Trigger Thumb Triploidy Trisomy 22 Tropical Spastic Paraparesis Tropical Sprue Trypanosomiasis Trypanosomiasis, Human East-African Tuberculous Meningitis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Tubulin, Beta Turner Syndrome Type Ii Mixed Cryoglobulinemia Typhoid Fever Tyrosinase-Like Tyrosinemia Tyrosinemia, Type Ii Ulcerative Colitis Ulnar Neuropathy Uremia Uremic Neuropathy Ureteral Obstruction Urinary Schistosomiasis Urticaria Usher Syndrome Usher Syndrome, Type I Usher Syndrome, Type Iia Uterine Carcinosarcoma Uterine Sarcoma Uveitis Vaccinia Vaginal Discharge Vaginitis Van Der Woude Syndrome 1 Vascular Dementia Vascular Disease Vascular Hemostatic Disease Vasculitis Venezuelan Equine Encephalitis Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Villous Adenocarcinoma Viral Encephalitis Viral Meningitis Virus-Associated Trichodysplasia Spinulosa Visceral Leishmaniasis Visceral Steatosis Vitamin E, Familial Isolated Deficiency of Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Vogt-Koyanagi-Harada Disease Vulvar Disease Vulvovaginal Gingival Syndrome Vulvovaginitis Wagner Syndrome Waldenstrom Macroglobulinemia Wallerian Degeneration Weber Syndrome Werner Syndrome Western Equine Encephalitis West Nile Virus Whim Syndrome Whiplash Wilms Tumor 1 Wilms Tumor 6 Wilson-Turner X-Linked Mental Retardation Syndrome Witkop Syndrome Wolfram Syndrome Wolfram Syndrome 1 Wrinkly Skin Syndrome Xanthinuria Xanthinuria, Type Ii Xanthogranulomatous Cholecystitis Xeroderma Pigmentosum, Complementation Group B X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome X-Ray Sensitivity Yaws Yemenite Deaf-Blind Hypopigmentation Syndrome Zollinger-Ellison Syndrome