Informaţii despre

Nume Pdgfrb-Associated Chronic Eosinophilic Leukemia
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Clasificare globală Malacards Boli rare; Bolile canceroase

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Boli A-Z Acute Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Promyelocytic Leukemia Adenocarcinoma Aging Aleukemic Mast Cell Leukemia 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 Amyloidosis Angioimmunoblastic T-Cell Lymphoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aortitis Aphasia Aplastic Anemia Arthrochalasia Ehlers-Danlos Syndrome Atypical Chronic Myeloid Leukemia Autoimmune Disease Blastic Plasmacytoid Dendritic Cell Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bone Marrow Cancer Breast Cancer Burkitt Lymphoma Calciphylaxis Cardiac Tamponade Chromosomal Triplication Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Colorblindness, Partial, Protan Series Cutaneous Mastocytosis Demyelinating Polyneuropathy Dendritic Cell Tumor Dermatitis Dermatitis Herpetiformis Diphtheria Disseminated Intravascular Coagulation Endometrial Adenocarcinoma Essential Thrombocythemia Ewing Sarcoma Factor Xiii Deficiency Familial Mediterranean Fever Follicular Mucinosis Folliculitis Gastric Cancer Generalized Eruptive Histiocytosis Germ Cells Tumors Gingivitis Graft-Versus-Host Disease Granuloma Annulare Granulomatous Dermatitis Hematopoietic Stem Cell Transplantation Hepatic Adenomas, Familial Hepatocellular Carcinoma Hereditary Wilms' Tumor Histiocytic Sarcoma Histiocytosis Juvenile Myelomonocytic Leukemia Large Granular Lymphocyte Leukemia Leukemia Leukostasis Liver Disease Lupus Erythematosus Lymphoblastic Leukemia Lymphoma Malignant Histiocytosis Mast Cell Disease Mast-Cell Leukemia Melanoma-Astrocytoma Syndrome Meningitis Miller-Dieker Lissencephaly Syndrome Mixed Germ Cell Tumor Monocytic Leukemia Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloperoxidase Deficiency Myeloproliferative Disorder, Chronic, with Eosinophilia Myeloproliferative Neoplasm Neuropathy Neutropenia Papular Mucinosis Pericardial Effusion Philadelphia-Negative Chronic Myeloid Leukemia Platelet Disorder, Familial, with Associated Myeloid Malignancy Pneumonia Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polyneuropathy Porphyria Porphyria Cutanea Tarda Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Purpura Pyoderma Pyoderma Gangrenosum Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Refractory Anemia Refractory Anemia with Excess Blasts Relapsing Polychondritis Retroperitoneal Fibrosis Sarcoidosis 2 Sarcoma Severe Congenital Neutropenia Skin Disease Small Intestinal Sarcoma Splenomegaly Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Systemic Lupus Erythematosus Systemic Mastocytosis T-Cell Large Granular Lymphocyte Leukemia Temporal Arteritis Thrombocytopenia Thrombotic Thrombocytopenic Purpura Urticaria Vasculitis
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