Informaţii despre

Nume Sickle Cell Disease
Pagina Web www.malacards.org
Clasificari ICD10 Sickle-cell disorders
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge

Vezi şi

Boli A-Z Acquired Methemoglobinemia Acute Chest Syndrome Acute Erythroid Leukemia Acute Necrotizing Encephalitis Acute Necrotizing Encephalopathy Type 1 Acute Poststreptococcal Glomerulonephritis Aging Albinism Albinism, Oculocutaneous, Type Ii Alcohol Abuse Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Amenorrhea Aneurysm Angioid Streaks Aniridia 1 Ankylosis Anorexia Nervosa 1 Appendicitis Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Aural Atresia, Congenital Autoimmune Hepatitis Babesiosis Bacteriuria Beta-Thalassemia Biliary Tract Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Marrow Necrosis Brain Injury Branch Retinal Artery Occlusion Breast Cancer Bronchial Disease Calciphylaxis Cardiac Conduction Defect Carnitine Deficiency, Systemic Primary Carotid Artery Occlusion Cataract 5, Multiple Types Cauda Equina Syndrome Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebritis Cerebrovascular Disease Cervicitis Chiari Malformation Chlamydia Choledocholithiasis Cholelithiasis Cholestasis Chromhidrosis Chronic Pain Chronic Thromboembolic Pulmonary Hypertension Cocaine Abuse Cold Agglutinin Disease Colonic Pseudo-Obstruction Complement Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Disorder of Glycosylation, Type Iic Congenital Hemolytic Anemia Congenital Methemoglobinemia Connective Tissue Disease Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cystic Fibrosis Darier-White Disease Deficiency Anemia Dextrocardia Diabetes Mellitus Disease_ontology Duodenal Ulcer Duodenitis Ectodermal Dysplasia Encephalitis Encephalopathy Endotheliitis End Stage Renal Failure Epidural Abscess Fanconi Anemia, Complementation Group E Fetal Hemoglobin Quantitative Trait Locus 1 Gallbladder Disease Gilbert Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glomerulonephritis Glucosephosphate Dehydrogenase Deficiency Glutathione Peroxidase Deficiency Gout Haemophilus Influenzae Haim-Munk Syndrome Heinz Body Anemias Hematopoietic Stem Cell Transplantation Hemoglobin C Disease Hemoglobin D Disease Hemoglobin E Disease Hemoglobin H Disease Hemoglobin Lepore-Beta-Thalassemia Syndrome Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hemosiderosis Hepatitis Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome Hereditary Spherocytosis Histiocytosis-Lymphadenopathy Plus Syndrome Human Coronavirus Sensitivity Hyperparathyroidism Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoaldosteronism Hypochromic Microcytic Anemia Hypogonadism Hypophosphatemic Bone Disease Hyporeninemic Hypoaldosteronism Hypoxia Ichthyosis Prematurity Syndrome Immune-Complex Glomerulonephritis Influenza Insulin-Like Growth Factor I Intracranial Aneurysm Intrahepatic Cholestasis Ischemia Juvenile Polymyositis Juvenile Rheumatoid Arthritis Kernicterus Kluver-Bucy Syndrome Labyrinthitis Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lissencephaly 1 Lung Disease Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome Lupus Erythematosus Macular Dystrophy, Retinal, 1, North Carolina Type Malaria Malignant Secondary Hypertension Mast Cell Activation Syndrome Membranoproliferative Glomerulonephritis Meningitis Methemoglobinemia Methemoglobinemia, Beta-Globin Type Microcytic Anemia Mild Pre-Eclampsia Mononeuropathy Moyamoya Disease 1 Mycoplasmal Pneumonia Myeloid Leukemia Myocardial Infarction Neonatal Abstinence Syndrome Neonatal Anemia Neonatal Jaundice Nephrotic Syndrome Neuropathy Neutropenia Neutrophilic Dermatosis, Acute Febrile Oculocutaneous Albinism Osgood-Schlatter's Disease Osteomyelitis Osteonecrosis Paraplegia Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Peritonitis Pernicious Anemia Phaeochromocytoma Pituitary Adenoma, Prolactin-Secreting Plasmodium Falciparum Malaria Plastic Bronchitis Pneumococcal Meningitis Pneumonia Polymyositis Portal Vein Thrombosis Priapism Primary Hyperparathyroidism Protein S Deficiency Pseudoxanthoma Elasticum Pulmonary Embolism Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pyomyositis Pyruvate Kinase Deficiency of Red Cells Rapp-Hodgkin Syndrome Retinal Artery Occlusion Retinal Vein Occlusion Retinitis Retinitis Pigmentosa Rheumatic Heart Disease Rheumatoid Arthritis Rosai-Dorfman Disease Sarcoidosis 2 Schimmelpenning-Feuerstein-Mims Syndrome Schistosomiasis Schnyder Corneal Dystrophy Sensorineural Hearing Loss Septic Arthritis Severe Congenital Neutropenia Sickle Beta Thalassemia Sickle Cell Anemia Siderosis Situs Inversus Sleep Apnea Slipped Capital Femoral Epiphysis Spinal Cord Infarction Splenic Abscess Splenic Infarction Splenic Sequestration Splenomegaly Spondyloarthropathy Spondyloocular Syndrome Stuttering Subacute Cerebellar Degeneration Substance Dependence Sudden Arrhythmia Death Syndrome Sudden Sensorineural Hearing Loss Superior Semicircular Canal Dehiscence Systemic Lupus Erythematosus Tay-Sachs Disease Thalassemia Thoracoabdominal Syndrome Thrombocytosis Thrombophilia Thrombosis Tonsillitis Traumatic Brain Injury Waterhouse-Friderichsen Syndrome