Informaţii despre

Nume Thrombotic Thrombocytopenic Purpura
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Thrombotic microangiopathy
Clasificare anatomică Malacards Boli de sânge; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Thrombotic Thrombocytopenic Purpura, Acquired; Thrombotic Thrombocytopenic Purpura, Congenital

Vezi şi

Boli A-Z Acquired Immunodeficiency Syndrome Acute Myocardial Infarction Acute Pancreatitis Adenocarcinoma Adenoma Adie Pupil Afibrinogenemia Aging Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Anca-Associated Vasculitis Androgen Insensitivity, Partial Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Arteriovenous Fistula Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Autoimmune Disease Autoimmune Hepatitis Autoimmune Pancreatitis Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Bombay Phenotype Bone Marrow Necrosis Boutonneuse Fever Breast Cancer Brucellosis Buerger Disease Buschke-Ollendorff Syndrome Carotid Artery Dissection Carotid Artery Occlusion Carotid Artery Thrombosis Castleman Disease Catastrophic Antiphospholipid Syndrome Cavernous Hemangioma Central Retinal Vein Occlusion Cerebellar Degeneration-Related Autoantigen 3 Cerebral Sinovenous Thrombosis Cerebritis Charcot-Marie-Tooth Disease Chikungunya Cholecystitis Chronic Myelomonocytic Leukemia Colitis Collagen Disease Complement Factor H Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Bile Acid Synthesis Defect Connective Tissue Disease Coronary Thrombosis Cortical Blindness Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crescentic Glomerulonephritis Crimean-Congo Hemorrhagic Fever Crohn's Colitis Crohn's Disease Crouzon Syndrome with Acanthosis Nigricans Cytomegalovirus Infection Diabetes Insipidus Diabetic Angiopathy Diffuse Scleroderma Disseminated Intravascular Coagulation Duodenitis Duodenum Cancer Eclampsia Ehrlichiosis Encephalopathy Endocarditis Endophthalmitis Endotheliitis Enterocolitis Epithelial Recurrent Erosion Dystrophy Erythromelalgia Essential Thrombocythemia Factor Xii Deficiency Focal Segmental Glomerulosclerosis Fontaine Progeroid Syndrome Gastric Cancer Glanzmann Thrombasthenia Glomerulonephritis Graves' Disease Hairy Cell Leukemia Headache Hellp Syndrome Hemangioma Hemoglobin C Disease Hemoglobin E Disease Hemoglobin H Disease Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hemolytic Uremic Syndrome, Atypical 1 Hemophilia Hemophilia a Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Veno-Occlusive Disease Hepatitis Hepatitis C Hepatitis C Virus Hereditary Spherocytosis Herpes Simplex Hydatidiform Mole, Recurrent, 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypereosinophilic Syndrome Hyper Ige Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoglycemia Igg4-Related Disease Immune System Disease Inflammatory Bowel Disease 1 Influenza Intermittent Claudication Intervertebral Disc Disease Intracranial Thrombosis Ischemia Juvenile Myelomonocytic Leukemia Kaposi Sarcoma Legg-Calve-Perthes Disease Leukemia Limited Scleroderma Liver Cirrhosis Lung Cancer Lupus Erythematosus Malignant Hypertension Malignant Peritoneal Mesothelioma Melanoma Melioidosis Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningoencephalitis Mitochondrial Dna Depletion Syndrome 4a Mixed Connective Tissue Disease Moyamoya Disease 1 Multicentric Castleman Disease Multiple Sclerosis Myelodysplastic Syndrome Myeloma, Multiple Myocardial Infarction Pancreatitis Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Peritoneal Mesothelioma Peritonitis Pernicious Anemia Pituitary Adenoma Plague Platelet Aggregation, Spontaneous Pneumonia Polyarteritis Nodosa Polymyositis Pre-Eclampsia Preeclampsia/eclampsia 1 Pregnancy Loss, Recurrent 1 Priapism Primary Thrombocytopenia Prostate Cancer Prostatitis Protein S Deficiency Prothrombin Deficiency Psoriasis Psoriasis 13 Pure Red-Cell Aplasia Purpura Purpura Fulminans Qualitative Platelet Defect Rabies Rapidly Progressive Glomerulonephritis Raynaud Disease Recurrent Acute Pancreatitis Retinal Detachment Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Reversible Cerebral Vasoconstriction Syndrome Rheumatoid Arthritis Rocky Mountain Spotted Fever Sarcoma Satb2-Associated Syndrome Severe Pre-Eclampsia Shwartzman Phenomenon Sjogren Syndrome Splenic Infarction Spotted Fever Status Epilepticus Stroke, Ischemic Subacute Bacterial Endocarditis Systemic Lupus Erythematosus Systemic Lupus Erythematosus 5 Takayasu Arteritis Thalassemia Thrombocytopenia Thrombocytopenic Purpura, Autoimmune Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombosis Thrombotic Thrombocytopenic Purpura, Acquired Thrombotic Thrombocytopenic Purpura, Congenital Thymoma Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tooth Disease Undifferentiated Pleomorphic Sarcoma Unilateral Absence of a Pulmonary Artery Uremia Vaginitis Vascular Disease Vasculitis Vitamin B12 Deficiency Von Willebrand's Disease Von Willebrand Disease, Type 1 Wiskott-Aldrich Syndrome