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Nume Thrombocytosis
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Boli A-Z Acquired Idiopathic Sideroblastic Anemia Acquired Polycythemia Acquired Thrombocytopenia Acquired Von Willebrand Syndrome Actinomycosis Acute Cholangitis Acute Leukemia Acute Monoblastic Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myocardial Infarction Acute Promyelocytic Leukemia Adenocarcinoma Afibrinogenemia, Congenital Aging Alcoholic Hepatitis Alpha-2-Plasmin Inhibitor Deficiency 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 Amegakaryocytic Thrombocytopenia, Congenital Analbuminemia Anemia of Prematurity Angina Pectoris Angiodysplasia Angiofollicular Lymph Hyperplasia Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aplastic Anemia Arteries, Anomalies of Arteriovenous Fistula Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Polyendocrine Syndrome Bacterial Meningitis B-Cell Growth Factor Beta-Thalassemia Bilateral Massive Adrenal Hemorrhage Bladder Cancer Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Bone Marrow Cancer Branch Retinal Artery Occlusion Breast Cancer Breast Reconstruction Bronchiolitis Budd-Chiari Syndrome Burns Caffey Disease Cardiogenic Shock Carotid Artery Thrombosis Cartilage Disease Castleman Disease Celiac Disease 1 Central Nervous System Disease Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Cervical Cancer Cervicitis Cholangitis Chromosomal Triplication Chromosome 5q Deletion Syndrome Chronic Eosinophilic Pneumonia Chronic Inflammatory Demyelinating Polyneuropathy Cold Agglutinin Disease Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Congestive Heart Failure Coronary Thrombosis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crescentic Glomerulonephritis Cryopyrin-Associated Periodic Syndrome Cyclic Neutropenia Deficiency Anemia Demyelinating Polyneuropathy Dengue Hemorrhagic Fever Dermatitis Diabetes Insipidus Diabetes Mellitus Diabetic Foot Ulcers Disseminated Intravascular Coagulation Down Syndrome Dyskeratosis Congenita, Autosomal Dominant 6 Endocarditis Endocardium Disease Endometrial Cancer Endotheliitis End Stage Renal Failure Eosinophilic Gastroenteritis Eosinophilic Pneumonia Erythrocytosis, Familial, 1 Erythromelalgia Essential Thrombocythemia Factor V Deficiency Factor Vii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Felty Syndrome Fetal Hydantoin Syndrome Fibrillary Glomerulonephritis Folic Acid Deficiency Anemia Fournier Gangrene Gastric Cancer Gastroenteritis Generalized Atherosclerosis Giant Hemangioma Glanzmann Thrombasthenia Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glomerulonephritis Hematologic Cancer Hemoglobinuria Hemolytic Anemia Hemophilia Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis C Hepatoblastoma Hepatocellular Carcinoma Hereditary Spherocytosis Histiocytosis Homocysteinemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Infective Endocarditis Inflammatory Bowel Disease Inflammatory Myofibroblastic Tumor Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Iritis Iron Deficiency Anemia Iron Metabolism Disease Ischemia Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Juvenile Rheumatoid Arthritis Kawasaki Disease Korean Hemorrhagic Fever Langerhans Cell Histiocytosis Leech Infestation Legg-Calve-Perthes Disease Leptospirosis Leukemia Leukemia, Chronic Myeloid Limb Ischemia Liver Cirrhosis Lung Benign Neoplasm Lung Cancer Lung Large Cell Carcinoma Lupus Erythematosus Lymphoma Macrocytic Anemia Malignant Otitis Externa Malignant Peritoneal Mesothelioma Marantic Endocarditis Megakaryocytic Leukemia Melanoma Meningitis Miliaria Miliaria Rubra Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Monocytic Leukemia Multicentric Castleman Disease Multiple Sclerosis Myasthenia Gravis Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloproliferative Neoplasm Myocardial Infarction Nephrotic Syndrome Nervous System Disease Neurofibromatosis, Type Iv, of Riccardi Neuropathy Neutrophilia, Hereditary Nutritional Deficiency Disease Oral Squamous Cell Carcinoma Ovarian Cancer Pancreatic Cancer Pancreatitis Pancytopenia Panniculitis Papillary Conjunctivitis Papilledema Paraneoplastic Syndromes Paroxysmal Nocturnal Hemoglobinuria Pasteurella Multocida Infection Perinatal Necrotizing Enterocolitis Peripheral Artery Disease Peripheral Vertigo Peritoneal Mesothelioma Peritonitis Pheochromocytoma Placenta Disease Platelet Aggregation, Spontaneous Plummer Vinson Syndrome Pneumonia Poems Syndrome Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polyneuropathy Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Primary Polycythemia Primary Thrombocytopenia Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudohypoaldosteronism Psoriatic Arthritis Ptosis Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Fibrosis Pulmonary Hypertension Pulmonary Tuberculosis Purpura Purpura Fulminans Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Q Fever Qualitative Platelet Defect Refractory Anemia Relapsing Polychondritis Respiratory Syncytial Virus Infectious Disease Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rheumatoid Arthritis Sagittal Sinus Thrombosis Seborrheic Infantile Dermatitis Secondary Syphilis Severe Congenital Neutropenia Sickle Cell Disease Sideroblastic Anemia Sneddon Syndrome Spastic Ataxia, Charlevoix-Saguenay Type Spinal Cord Infarction Splenic Disease Splenic Infarction Splenomegaly Squamous Cell Carcinoma Stroke, Ischemic Subacute Thyroiditis Sudden Sensorineural Hearing Loss Syncope Syphilis Systemic Lupus Erythematosus Systemic Mastocytosis Takayasu Arteritis Temporal Arteritis Testicular Cancer Thalassemia Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thymoma Thyroiditis Toxocariasis Tremor Univentricular Heart Urticaria Urticaria Pigmentosa Uterine Corpus Serous Adenocarcinoma Vaginitis Valproate Embryopathy Varicose Veins Vascular Disease Vein Disease Venous Insufficiency Vibrio Vulnificus Infection Vitamin B12 Deficiency Von Willebrand's Disease Von Willebrand Disease, Type 1