Informaţii despre

Nume Essential Thrombocythemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Essential (haemorrhagic) thrombocythaemia
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
Boli din aceeaşi familie Thrombocythemia 1; Thrombocythemia 2; Thrombocythemia 3

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Polycythemia Acquired Thrombocytopenia Acquired Von Willebrand Syndrome Acrocallosal Syndrome Acute Biphenotypic Leukemia Acute Erythroid Leukemia Acute Leukemia Acute Myocardial Infarction Adult Oligodendroglioma Afibrinogenemia Afibrinogenemia, Congenital Aging Al Amyloidosis Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amegakaryocytic Thrombocytopenia, Congenital Analbuminemia Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Anemia of Prematurity Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Antiphospholipid Syndrome Aplastic Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Atypical Chronic Myeloid Leukemia Autoimmune Disease of Blood Autoimmune Lymphoproliferative Syndrome, Type V Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Bleeding Disorder, Platelet-Type, 16 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blue Toe Syndrome Bone Marrow Cancer Budd-Chiari Syndrome Burns Cardiac Tamponade Carotid Artery Dissection Carotid Artery Thrombosis Cellular Congenital Mesoblastic Nephroma Cellular Neurofibroma Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebritis Cholecystitis Chondroblastic Osteosarcoma Choroiditis Chronic Monocytic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Chronic Venous Insufficiency Chylomicron Retention Disease Cold Agglutinin Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Thrombosis Cryoglobulinemia, Familial Mixed Diabetes Mellitus Dilated Cardiomyopathy Disseminated Intravascular Coagulation Dyskeratosis Congenita, Autosomal Dominant 6 Enchondroma Endotheliitis Erythrocytosis, Familial, 1 Erythromelalgia Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor X Deficiency Fibrillary Astrocytoma Focal Segmental Glomerulosclerosis Folic Acid Deficiency Anemia Giant Hemangioma Glanzmann Thrombasthenia Glioma Susceptibility 1 Granulocytopenia Gray Platelet Syndrome Hairy Cell Leukemia Headache Hematopoietic Stem Cell Transplantation Hemoglobin C Disease Hemopericardium Hemophilia Hemophilia a Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Infectious Anterior Uveitis Infective Endocarditis Inherited Blood Coagulation Disease Inherited Predisposition to Essential Thrombocythemia Intermittent Claudication Interval Angle-Closure Glaucoma Intracranial Chondrosarcoma Intracranial Hypertension Iron-Refractory Iron Deficiency Anemia Ischemia Ischemic Colitis Korean Hemorrhagic Fever Large Granular Lymphocyte Leukemia Legg-Calve-Perthes Disease Leukemia Leukemia, Chronic Myeloid Lung Cancer Lymphoblastic Leukemia Lymphoma Lymphomatoid Granulomatosis Marantic Endocarditis Mast Cell Disease Maxillary Sinus Squamous Cell Carcinoma Megakaryocytic Leukemia Menkes Disease Moyamoya Disease 1 Mycosis Fungoides Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloperoxidase Deficiency Myeloproliferative Neoplasm Myocardial Infarction Neovascular Glaucoma Pancytopenia Paraplegia Parkinsonism with Spasticity, X-Linked Pdgfrb-Associated Chronic Eosinophilic Leukemia Phacomatosis Pigmentovascularis Philadelphia-Negative Chronic Myeloid Leukemia Placental Insufficiency Plantar Wart Plasmablastic Lymphoma Platelet Aggregation, Spontaneous Platelet Membrane Fluidity Polycythemia Polycythemia Vera Porphyria Variegata Portal Hypertension Portal Vein Thrombosis Primary Polycythemia Primary Thrombocytopenia Protein Z Deficiency Prothrombin Deficiency Psoriasis 2 Psoriasis 7 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulmonary Sarcoidosis Purpura Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Qualitative Platelet Defect Quebec Platelet Disorder Refractory Anemia Refractory Anemia with Excess Blasts Renovascular Hypertension Retinal Artery Occlusion Retinal Vein Occlusion Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rheumatoid Arthritis Riddle Syndrome Sarcoidosis 2 Sarcoma Scott Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwartzman Phenomenon Splenic Disease Splenomegaly Spondylitis Spondyloarthropathy 1 Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Spotted Fever Squamous Cell Papilloma Stroke, Ischemic Systemic Mastocytosis T-Cell Large Granular Lymphocyte Leukemia Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 1 Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombosis Thrombotic Thrombocytopenic Purpura Undifferentiated Pleomorphic Sarcoma Unilateral Absence of a Pulmonary Artery Venous Insufficiency Von Willebrand's Disease Von Willebrand Disease, Type 1