Informaţii despre

Nume Macroglobulinemia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice
Clasificari ICD10 Waldenstr

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Boli A-Z Acute Kidney Tubular Necrosis Acute Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Agammaglobulinemia Aging Aids Dementia Complex Al Amyloidosis Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aminoaciduria Amyloid Neuropathy Amyloidosis Angioedema Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Aphasia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Atrial Fibrillation Autoimmune Disease Autoimmune Lymphoproliferative Syndrome, Type V Autonomic Neuropathy B Cell Deficiency B-Cell Lymphomas Birdshot Chorioretinopathy Blastic Plasmacytoid Dendritic Cell Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Breast Cancer Bullous Pemphigoid Cellulitis Central Nervous System Lymphoma Central Retinal Vein Occlusion Chops Syndrome Choroiditis Chromosomal Triplication Chromosome 6q Deletion Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Cleft Lip/palate with Abnormal Thumbs and Microcephaly Cold Agglutinin Disease Colitis Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hypogammaglobulinemia Connective Tissue Disease Cryoglobulinemia Cryptococcal Meningitis Cytomegalic Inclusion Disease Demyelinating Polyneuropathy Diffuse Large B-Cell Lymphoma Discoid Lupus Erythematosus Duodenitis Eosinophilic Colitis Evans' Syndrome Extramedullary Plasmacytoma Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fanconi Syndrome Fibrogenesis Imperfecta Ossium Gastric Ulcer Glomerulonephritis Hairy Cell Leukemia Hansen's Disease Heavy Chain Disease Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemochromatosis, Type 2a Hemolytic Anemia Hepatic Adenomas, Familial Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Human Coronavirus Sensitivity Human Immunodeficiency Virus Infectious Disease Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoglycemia Hypophosphatemia Hypoxia Immune Deficiency Disease Immunodeficiency with Hyper-Igm, Type 1 Immunodeficiency with Hyper-Igm, Type 4 Immunoglobulin a Deficiency 1 Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Intestinal Disease Intraocular Lymphoma Kaposiform Hemangioendothelioma Lateral Sclerosis Lepromatous Leprosy Leukemia Light Chain Deposition Disease Lupus Erythematosus Lymphangiectasia, Intestinal Lymph Node Disease Lymphoblastic Leukemia Lymphoma Lymphoma, Hodgkin, Classic Lymphoma, Mucosa-Associated Lymphoid Type Lymphoma, Non-Hodgkin, Familial Lymphomatoid Papulosis Lymphoplasmacytic Lymphoma Lymphoproliferative Syndrome 2 Mantle Cell Lymphoma Marginal Zone B-Cell Lymphoma Maxillary Sinusitis Membranoproliferative Glomerulonephritis Membranous Nephropathy Mesenteric Vascular Occlusion Miyoshi Muscular Dystrophy 1 Monoclonal Gammopathy of Uncertain Significance Monoclonal Paraproteinemia Monocytic Leukemia Mononeuritis Multiplex Mu Chain Disease Multiple Sclerosis Myelodysplastic Syndrome Myeloid Leukemia Myeloma, Multiple Nasopharyngitis Necrobiotic Xanthogranuloma Nephrotic Syndrome Neuritis Neuropathy Nodular Regenerative Hyperplasia Non-Involuting Congenital Hemangioma Optic Neuritis Orbital Cancer Osteomyelitis Osteonecrosis Osteonecrosis of the Jaw Pancreatitis Pancreatitis, Hereditary Pancytopenia Paraneoplastic Syndromes Peliosis Hepatis Perinephritis Phelan-Mcdermid Syndrome Plasma Cell Leukemia Plasmacytoma Plasma Protein Metabolism Disease Pneumonia Poems Syndrome Polyclonal Hypergammaglobulinemia Polycythemia Polycythemia Vera Polyneuropathy Polyneuropathy Associated with Igm Monoclonal Gammapathy with Anti-Mag Portal Hypertension Primary Central Nervous System Lymphoma Progressive Multifocal Leukoencephalopathy Proliferative Glomerulonephritis Prolymphocytic Leukemia Protein-Losing Enteropathy Psoriasis Psoriasis 13 Pulmonary Hypertension Pure Red-Cell Aplasia Rapidly Progressive Glomerulonephritis Renal Tubular Acidosis Retinal Degeneration Retinal Detachment Retinal Vein Occlusion Retinitis Rheumatoid Arthritis Rosacea Schnitzler Syndrome Scleritis Selective Immunoglobulin Deficiency Disease Sinusitis Splenic Marginal Zone Lymphoma Splenomegaly Steatorrhea Stomatin-Like Protein-2, Hyperphosphorylation of Sveinsson Chorioretinal Atrophy T-Cell Lymphoma 1a Temporal Arteritis Thoracoabdominal Syndrome Thrombocytopenia Thrombosis Tibia, Hypoplasia or Aplasia of, with Polydactyly Tonsillitis Toxoplasmoză Tremor Urticaria Vasculitis Waldenstrom Macroglobulinemia Whim Syndrome Williams-Beuren Syndrome Xanthoma Disseminatum