Informaţii despre

Nume Polycythemia Vera
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Polycythaemia vera
Clasificare anatomică Malacards Boli de sânge

Vezi şi

Boli A-Z Acquired Polycythemia Acquired Von Willebrand Syndrome Acrocallosal Syndrome Acute Erythroid Leukemia Acute Myocardial Infarction Acute Necrotizing Encephalitis Acute Necrotizing Encephalopathy Type 1 Acute Non Lymphoblastic Leukemia Acute Zonal Occult Outer Retinopathy Adenoma Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Capillary Dysplasia Alzheimer Disease 3 Amaurosis Fugax Amegakaryocytic Thrombocytopenia, Congenital Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Anemia of Prematurity Aneurysm Angiomyolipoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aortic Valve Disease 2 Aplastic Anemia Aquagenic Pruritus Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Atrial Fibrillation Atypical Chronic Myeloid Leukemia Autoimmune Disease of Blood Axonal Neuropathy Back Pain B Cell Linker Protein Deficiency B-Cell Lymphomas Bilateral Massive Adrenal Hemorrhage Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Bone Marrow Cancer Bone Marrow Necrosis Budd-Chiari Syndrome Burns Capillary Leak Syndrome Cellular Congenital Mesoblastic Nephroma Cellular Neurofibroma Central Retinal Artery Occlusion Cerebritis Cervical Rib Cervicitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chromophobe Renal Cell Carcinoma Chromosomal Triplication Chromosome 5q Deletion Syndrome Chronic Eosinophilic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Artery Dissection, Spontaneous Crouzon Syndrome with Acanthosis Nigricans Deep Leiomyoma Dermatitis Desmoid Tumor Diffuse Large B-Cell Lymphoma Disseminated Intravascular Coagulation Duodenitis Duodenum Cancer Dyskeratosis Congenita, Autosomal Dominant 6 Dysplastic Nevus Syndrome Encephalitis Endotheliitis Eosinophilic Pustular Folliculitis Erdheim-Chester Disease Erythrocytosis, Familial, 1 Erythrocytosis, Familial, 2 Erythromelalgia Essential Thrombocythemia Ewing's Family of Tumors Fibrosarcoma of Bone Focal Segmental Glomerulosclerosis Folic Acid Deficiency Anemia Folliculitis Gastric Cancer Gastrointestinal Stromal Tumor Glomerulonephritis Granulocytopenia Granulomatous Dermatitis Hairy Cell Leukemia Heart Sarcoma Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Vascular Disease Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hereditary Spherocytosis Histiocytosis Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Hyperparathyroidism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoxia Insulin-Like Growth Factor I Ischemia Ischemic Optic Neuropathy Isolated Growth Hormone Deficiency, Type Ii Jak3-Deficient Severe Combined Immunodeficiency Kidney Fibrosarcoma Lactocele Legg-Calve-Perthes Disease Leukemia Leukemia, Chronic Myeloid Lymphoblastic Leukemia Lymphoma Lymphoplasmacytic Lymphoma Macroglobulinemia Malignant Histiocytosis Malignant Spiradenoma Mast Cell Disease Mast Cell Neoplasm Meckel Syndrome, Type 1 Mediastinitis Megakaryocytic Leukemia Megaloblastic Anemia Membranoproliferative Glomerulonephritis Mitochondrial Dna Depletion Syndrome 4a Mixed Lacrimal Gland Cancer Mycosis Fungoides Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 Myeloid Leukemia Myeloid Sarcoma Myelophthisic Anemia Myeloproliferative Neoplasm Myocardial Infarction Myoma Myopathy, Distal, 5 Nephrotic Syndrome Neurofibroma Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuropathy Neutrophilia, Hereditary Pancreatitis Pancytopenia Papilledema Parathyroid Adenoma Parathyroid Carcinoma Parkinsonism with Spasticity, X-Linked Pdgfrb-Associated Chronic Eosinophilic Leukemia Pelger-Huet Anomaly Perinephritis Peritonitis Phacomatosis Pigmentovascularis Piebald Trait Plasmablastic Lymphoma Platelet Membrane Fluidity Plexopathy Pneumonia Poems Syndrome Polycythemia Polyneuropathy Porphyria Variegata Portal Hypertension Portal Vein Thrombosis Primary Hypereosinophilic Syndrome Primary Hyperparathyroidism Primary Polycythemia Primary Thrombocytopenia Progressive Multifocal Leukoencephalopathy Prostatitis Psoriasis 1 Psoriasis 11 Psoriasis 13 Psoriasis 2 Psoriasis 7 Pulmonary Embolism Pulmonary Hypertension Pulmonary Sarcoidosis Purpura Pyoderma Pyoderma Gangrenosum Rapidly Progressive Glomerulonephritis Refractory Anemia Refractory Anemia with Excess Blasts Reticular Perineurioma Retinal Artery Occlusion Retinal Vein Occlusion Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Sarcoidosis 2 Sarcoma Severe Congenital Neutropenia Sm-Ahnmd Spinal Cord Infarction Splenic Abscess Splenic Infarction Splenic Marginal Zone Lymphoma Splenomegaly Systemic Capillary Leak Syndrome Systemic Mastocytosis T-Cell Prolymphocytic Leukemia Thalassemia Thrombasthenia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombosis Transient Erythroblastopenia of Childhood Undifferentiated Pleomorphic Sarcoma Urticaria Urticaria Pigmentosa Vascular Disease Vasculitis Waldenstrom Macroglobulinemia