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Boli A-Z Acute Leukemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Anuria Arthrochalasia Ehlers-Danlos Syndrome Atypical Hemolytic-Uremic Syndrome with H Factor Anomaly Autoinflammation with Infantile Enterocolitis Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen C3 Glomerulopathy Catastrophic Antiphospholipid Syndrome Complement Factor B Deficiency Complement Factor H Deficiency Degeneration of Macula and Posterior Pole Dense Deposit Disease Diarrhea Diffuse Alveolar Hemorrhage Endotheliitis End Stage Renal Failure Enterocolitis Eosinophilic Granulomatosis with Polyangiitis Factor Xii Deficiency Genetic Atypical Hemolytic-Uremic Syndrome Glomerulonephritis Hellp Syndrome Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hepatic Adenomas, Familial Hepatitis Hepatitis B Homocystinuria Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Influenza Kuhnt-Junius Degeneration Leukemia Lupus Erythematosus Lymphoblastic Leukemia Macular Degeneration, Age-Related, 1 Malignant Hypertension Membranoproliferative Glomerulonephritis Mesangial Proliferative Glomerulonephritis Nephrotic Syndrome, Type 7 Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis Paroxysmal Nocturnal Hemoglobinuria Pediatric Systemic Lupus Erythematosus Peritonitis Pertussis Plasminogen Deficiency, Type I Proliferative Glomerulonephritis Purpura Retinitis Rheumatic Disease Systemic Lupus Erythematosus Tetraamelia Syndrome, Autosomal Recessive Thrombocytopenia Thrombophilia Thrombotic Thrombocytopenic Purpura Vasculitis