Informaţii despre

Nume Splenomegaly
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Splenomegaly, not elsewhere classified

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Boli A-Z Acquired Polycythemia Acute Erythroid Leukemia Acute Leukemia Acute Pancreatitis Adenocarcinoma Adenosquamous Carcinoma Agammaglobulinemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aneurysm Angiodysplasia Angiokeratoma Angiomatosis Angiosarcoma Aniridia 1 Ankylosis Anorexia Nervosa 1 Antiphospholipid Syndrome Aortic Aneurysm Arthritis Arthrochalasia Ehlers-Danlos Syndrome Atypical Chronic Myeloid Leukemia Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Pancreatitis Banti's Syndrome B-Cell Expansion with Nfkb and T-Cell Anergy B-Cell Lymphomas Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Marrow Cancer Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Small Vessel Disease with or Without Ocular Anomalies Brittle Bone Disorder Bronchopneumonia Budd-Chiari Syndrome Burns Cardiac Sarcoidosis Caroli Disease Cavernous Hemangioma Cerebritis Cholelithiasis Chronic Congestive Splenomegaly Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Coccidioidomycosis Colitis Colorectal Cancer Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Dyserythropoietic Anemia Congenital Hemolytic Anemia Congenital Hepatic Fibrosis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cystadenoma Cystic Fibrosis Cystic Lymphangioma Cytomegalovirus Infection Diabetes Mellitus Diarrhea Disseminated Intravascular Coagulation Drug-Induced Lupus Erythematosus Endocarditis Endomyocardial Fibrosis Endotheliitis Eosinophilia, Familial Eosinophilic Fasciitis Eosinophilic Gastroenteritis Erythrocytosis, Familial, 1 Essential Thrombocythemia Excessive Tearing Fabry Disease Familial Mediterranean Fever Fasciitis Filariasis Follicular Lymphoma Gamma Heavy Chain Disease Gastric Adenocarcinoma Gastroenteritis Gigantism Granuloma Inguinale Gray Platelet Syndrome Haim-Munk Syndrome Hairy Cell Leukemia Heavy Chain Disease Helicobacter Pylori Infection Hemangioma Hematopoietic Stem Cell Transplantation Hemoglobin H Disease Hemolytic Anemia Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hereditary Spherocytosis Histiocytic Sarcoma Histiocytosis Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Hypereosinophilic Syndrome Hyperglobulinemic Purpura Hyper Ige Syndrome Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Idiopathic Neutropenia Immunoglobulin E Concentration, Serum Infective Endocarditis Intussusception Iridocyclitis Langerhans Cell Histiocytosis Large Granular Lymphocyte Leukemia Lecithin:cholesterol Acyltransferase Deficiency Leishmaniasis Leukemia Leukemia, Chronic Myeloid Linitis Plastica Littoral Cell Angioma of the Spleen Liver Cirrhosis Liver Disease Lupus Erythematosus Lymphadenitis Lymphangioma Lymphangiomatosis Lymphoblastic Lymphoma Lymphoma Lymphoma, Hodgkin, Classic Lymphomatoid Granulomatosis Lymphopenia Lymphoplasmacytic Lymphoma Lymphoproliferative Syndrome Macroglobulinemia Malaria Malignant Histiocytosis Mantle Cell Lymphoma Mediastinitis Meester-Loeys Syndrome Megaloblastic Anemia Melanoma Microscopic Colitis Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Splenomegaly Myeloproliferative Neoplasm Myocarditis Neonatal Jaundice Nephrotic Syndrome Neutropenia Neutrophilia, Hereditary Niemann-Pick Disease Nodular Regenerative Hyperplasia Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia Opitz-Kaveggia Syndrome Pancreatic Cystadenoma Pancreatitis Pancytopenia Papillomatosis, Confluent and Reticulated Paracoccidioidomycosis Pdgfrb-Associated Chronic Eosinophilic Leukemia Peripheral T-Cell Lymphoma Peritonitis Pernicious Anemia Persistent Polyclonal B-Cell Lymphocytosis Peutz-Jeghers Syndrome Pfeiffer Syndrome Pharyngitis Pick Disease of Brain Plasma Cell Leukemia Pneumonia Polycythemia Polycythemia Vera Porphyria Portal Hypertension Portal Vein Thrombosis Primary Agammaglobulinemia Primary Polycythemia Prolidase Deficiency Prostatitis Pulmonary Embolism Pulmonary Hypertension Pulmonary Tuberculosis Purpura Pycnodysostosis Pyoderma Pyoderma Gangrenosum Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Q Fever Refractory Anemia Refractory Celiac Disease Retinitis Retinitis Pigmentosa and Erythrocytic Microcytosis Rhabdomyosarcoma Rheumatoid Arthritis Sarcoidosis 2 Sarcoma Scarlet Fever Schistosomiasis Sea-Blue Histiocyte Disease Sickle Cell Anemia Sickle Cell Disease Small Cell Carcinoma Splenic Abscess Splenic Artery Aneurysm Splenic Infarction Splenic Marginal Zone Lymphoma Splenic Sequestration Splenic Tuberculosis Splenomegaly, Cytopenia, and Vision Loss Spondyloocular Syndrome Systemic Lupus Erythematosus Systemic Mastocytosis T-Cell Large Granular Lymphocyte Leukemia T-Cell Leukemia Telangiectasis Thalassemia Thrombocytopenia Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombosis Thyroid Cancer Thyroiditis Tyrosinemia Vasculitis Visceral Leishmaniasis Vitamin B12 Deficiency Wandering Spleen Wolf-Hirschhorn Syndrome