Informaţii despre

Nume Thrombocytopenia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Thrombocytopenia, unspecified
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge
Boli din aceeaşi familie Acquired Thrombocytopenia; Primary Thrombocytopenia; Thrombocytopenia 1; Thrombocytopenia 2; Thrombocytopenia 3; Thrombocytopenia 4; Thrombocytopenia 5; Thrombocytopenia 6; Thrombocytopenia Due to Platelet Alloimmunization

Vezi şi

Boli A-Z Achondroplasia Acquired Amegakaryocytic Thrombocytopenia Acquired Generalized Lipodystrophy Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acquired Pure Red Cell Aplasia Acquired Thrombocytopenia Acute Adrenal Insufficiency Acute Disseminated Encephalomyelitis Acute Leukemia Acute Lymphocytic Leukemia Acute Myocardial Infarction Acute Poststreptococcal Glomerulonephritis Acute Promyelocytic Leukemia Acute Pyelonephritis Adenocarcinoma Adenofibroma Adenomyosis Adie Pupil Adrenomyeloneuropathy Adult Respiratory Distress Syndrome Adult T-Cell Leukemia Afibrinogenemia Afibrinogenemia, Congenital Aging Alcoholic Hepatitis Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amegakaryocytic Thrombocytopenia, Congenital Amenorrhea Anauxetic Dysplasia 1 Androgen Insensitivity, Partial Androgen Insensitivity Syndrome Aneurysm Angioimmunoblastic T-Cell Lymphoma Angiomatosis Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Anuria Aortic Aneurysm Aplastic Anemia Arteries, Anomalies of Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Arthus Reaction Ascending Cholangitis Aspergillosis Asplenia, Isolated Congenital Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Atrial Fibrillation Atrioventricular Block Autoimmune Disease Autoimmune Disease of Blood Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Pancreatitis Autoinflammation with Infantile Enterocolitis Autosomal Dominant Macrothrombocytopenia Autosomal Thrombocytopenia with Normal Platelets Ayme-Gripp Syndrome Babesiosis Bacterial Meningitis Bartonellosis B-Cell Lymphomas Bernard-Soulier Syndrome Beta-Thalassemia Bilateral Massive Adrenal Hemorrhage Biliary Atresia Bipolar Disorder 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 Rubber Bleb Nevus Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Marrow Cancer Breast Angiosarcoma Breast Cancer Brucellosis Budd-Chiari Syndrome Burns Buschke-Ollendorff Syndrome Capillary Leak Syndrome Cardiac Tamponade Cataract Catastrophic Antiphospholipid Syndrome Cavernous Hemangioma Cerebral Artery Occlusion Cerebral Hemorrhage Cerebritis Cerebrotendinous Xanthomatosis Cervicitis Chikungunya Choanal Atresia, Posterior Cholangitis Cholelithiasis Cholestasis Chorioangioma Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb Chromosome 5q Deletion Syndrome Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Inflammatory Demyelinating Polyneuropathy Chronic Myelomonocytic Leukemia Chronic Thromboembolic Pulmonary Hypertension Citrullinemia, Classic Cocaine Abuse Cockayne Syndrome Cohen Syndrome Cold Agglutinin Disease Colitis Colorado Tick Fever Colorectal Cancer Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Iic Congenital Hepatic Fibrosis Congenital Syphilis Connective Tissue Disease Cornelia De Lange Syndrome Coronary Thrombosis Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crimean-Congo Hemorrhagic Fever Cryoglobulinemia Cryptococcal Meningitis Cutaneous T Cell Lymphoma Cystitis Cytomegalic Inclusion Disease Cytomegalovirus Infection Cytomegalovirus Retinitis Dandy-Walker Complex Dementia Demyelinating Polyneuropathy Dengue Disease Dengue Hemorrhagic Fever Dengue Shock Syndrome Dengue Virus Dermatitis Dermatomyositis Diabetes Mellitus Diarrhea Diffuse Alveolar Hemorrhage Diffuse Neonatal Hemangiomatosis Digeorge Syndrome Diphtheria Discitis Disseminated Intravascular Coagulation Dk Phocomelia Syndrome Drug Dependence Drug-Induced Lupus Erythematosus Dwarfism Dyschromatosis Universalis Hereditaria Dyserythropoietic Anemia and Thrombocytopenia Dyskeratosis Congenita Dyskeratosis Congenita, Autosomal Dominant 6 Early Congenital Syphilis Eclampsia Ehrlichiosis Encephalitis Encephalocele Encephalopathy Endocarditis Endotheliitis Enterocolitis Eosinophilic Fasciitis Eosinophilic Pneumonia Epithelioid Hemangioendothelioma Epstein Syndrome Erdheim-Chester Disease Erythromelalgia Essential Thrombocythemia Evans' Syndrome Exanthem Exfoliative Dermatitis Extragonadal Germ Cell Cancer Factor V Deficiency Factor Vii Deficiency Factor Xiii Deficiency Fanconi Anemia, Complementation Group E Fasciitis Faye-Petersen-Ward-Carey Syndrome Felty Syndrome Fetal and Neonatal Alloimmune Thrombocytopenia Focal Segmental Glomerulosclerosis Follicular Lymphoma Galactose Epimerase Deficiency Galactosialidosis Gastric Cancer Gastric Neuroendocrine Tumor Gastroenteritis Genitopatellar Syndrome Geographic Tongue Germ Cells Tumors Gestational Diabetes Gianotti Crosti Syndrome Giant Cell Myocarditis Giant Hemangioma Gilles De La Tourette Syndrome Glanzmann Thrombasthenia Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Glioma Glomerulonephritis Glucocorticoid Resistance, Generalized Graft-Versus-Host Disease Granulocytopenia Granulomatous Hepatitis Graves' Disease Gray Platelet Syndrome Growth Control, Y-Chromosome Influenced Hairy Cell Leukemia Hashimoto Thyroiditis Helicobacter Pylori Infection Hellp Syndrome Hemangioendothelioma Hemangioma Hemangioma-Thrombocytopenia Syndrome Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis Hemophagocytic Reticulosis Hemophilia Hemophilia a Hemophilia B Hemorrhagic Cystitis Hemorrhagic Disease Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemosiderosis Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hepatosplenic T-Cell Lymphoma Hereditary Antithrombin Deficiency Hereditary Spherocytosis Histiocytic Sarcoma Histiocytoma Histiocytosis Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Horseshoe Kidney Human Coronavirus Sensitivity Hydrocephalus Hydronephrosis Hydrops Fetalis Hydrops Fetalis, Nonimmune Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypereosinophilic Syndrome Hyperinsulinism Hyperparathyroidism Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypervitaminosis a Hypoglycemia Hypokalemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Ichthyosis Prematurity Syndrome Igg4-Related Disease Immune-Complex Glomerulonephritis Immune Suppression Immune System Disease Immunoglobulin Alpha Deficiency Immunoglobulin E Concentration, Serum Infective Endocarditis Influenza Inherited Blood Coagulation Disease Insulinoma Interstitial Lung Disease Interstitial Nephritis Intestinal Pseudo-Obstruction Intracranial Aneurysm Intravascular Large B-Cell Lymphoma Iron Deficiency Anemia Ischemia Ischemic Optic Neuropathy Ivic Syndrome Jacobsen Syndrome Japanese Encephalitis Juvenile Myelomonocytic Leukemia Juvenile Rheumatoid Arthritis Langerhans Cell Histiocytosis Large Granular Lymphocyte Leukemia Laryngeal Adductor Paralysis Laryngeal Cleft Lathyrism Leptospirosis Leukemia Leukostasis Lipodystrophy Lipomatosis Lissencephaly 1 Listeriosis Liver Cirrhosis Liver Disease Localized Scleroderma Lung Cancer Lung Disease Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphadenitis Lymphangioma Lymphangitis Lymph Node Tuberculosis Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphocytic Hypophysitis Lymphoma Lymphoma, Hodgkin, Classic Lymphopenia Lymphoproliferative Syndrome Lymphosarcoma Macrocytic Anemia Macroglobulinemia Malaria Malignant Glioma Malignant Histiocytosis Malignant Hypertension Mantle Cell Lymphoma Marantic Endocarditis Mayer-Rokitansky-Kuster-Hauser Syndrome May-Thurner Syndrome Meconium Aspiration Syndrome Mediastinitis Megakaryocytic Leukemia Megaloblastic Anemia Melioidosis Meningitis Meningococcal Infection Meningococcemia Mercury Poisoning Mesenteric Lymphadenitis Metal Allergy Mevalonic Aciduria Microcytic Anemia Miliary Tuberculosis Miller-Dieker Lissencephaly Syndrome Mirage Syndrome Mitochondrial Dna Depletion Syndrome 4a Mitral Valve Stenosis Mixed Connective Tissue Disease Mixed-Type Autoimmune Hemolytic Anemia Mobitz Type Ii Atrioventricular Block Mononeuritis Multiplex Monosomy 21 Mucopolysaccharidosis, Type Vii Mucositis Multifocal Lymphangioendotheliomatosis with Thrombocytopenia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mungan Syndrome Musical Perfect Pitch Myasthenia Gravis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myelophthisic Anemia Myeloproliferative Neoplasm Myh-9 Related Disease Myh9 Related Thrombocytopenia Myhre Syndrome Myocardial Infarction Myocarditis Myopathy Myositis Neonatal Alloimmune Neutropenia Neonatal Anemia Neonatal Diabetes Mellitus Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neuroleptic Malignant Syndrome Neuropathy Neutropenia Neutrophilic Dermatosis, Acute Febrile Niemann-Pick Disease Niemann-Pick Disease, Type B Nocardiosis Non-Involuting Congenital Hemangioma Nonseminomatous Germ Cell Tumor Oculoectodermal Syndrome Oligodendroglioma Orbital Lymphangioma Osteochondrodysplasia Osteopetrosis Osteopetrosis, Autosomal Recessive 1 Ovarian Cancer Pancreatitis Pancytopenia Paraneoplastic Syndromes Paroxysmal Nocturnal Hemoglobinuria Pdgfrb-Associated Chronic Eosinophilic Leukemia Pediatric Systemic Lupus Erythematosus Pemphigoid Gestationis Pemphigus Pemphigus Foliaceus Pericardial Tuberculosis Pericarditis Periodontitis Periostitis Peripheral Artery Disease Pernicious Anemia Pertussis Pfeiffer Syndrome Phocomelia Pick Disease of Brain Pilocytic Astrocytoma Pituitary Apoplexy Pituitary Stalk Interruption Syndrome Pituitary Tumors Placental Abruption Plasmodium Falciparum Malaria Plasmodium Vivax Malaria Platelet Disorder, Familial, with Associated Myeloid Malignancy Platelet Glycoprotein Iv Deficiency Pleomorphic Rhabdomyosarcoma Plethora of Newborn Pneumonia Poems Syndrome Polycythemia Polycythemia Vera Polymicrogyria Polyneuropathy Porencephaly Porphyria Portal Hypertension Pre-Eclampsia Premature Centromere Division Primary Biliary Cirrhosis Primary Hyperparathyroidism Primary Thrombocytopenia Prolymphocytic Leukemia Prostate Cancer Prostatitis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Psoriasis Psoriasis 13 Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pure Red-Cell Aplasia Purpura Pyelonephritis Qualitative Platelet Defect Quebec Platelet Disorder Radin Blood Group Antigen Radioulnar Synostosis Radio-Ulnar Synostosis-Amegakaryocytic Thrombocytopenia Syndrome Rapidly Involuting Congenital Hemangioma Rapp-Hodgkin Syndrome Relapsing Fever Relapsing-Remitting Multiple Sclerosis Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinitis Retroperitoneal Fibrosis Rhabdomyosarcoma Rheumatic Heart Disease Rheumatoid Arthritis Rift Valley Fever Rocky Mountain Spotted Fever Rosai-Dorfman Disease Sagittal Sinus Thrombosis Sarcoidosis 2 Sarcoma Schistosomiasis Schizencephaly Schizoaffective Disorder Scleromyxedema Scott Syndrome Scrub Typhus Sea-Blue Histiocyte Disease Severe Acute Respiratory Syndrome Severe Combined Immunodeficiency Severe Congenital Neutropenia Severe Pre-Eclampsia Sickle Beta Thalassemia Sideroblastic Anemia Siderosis Sitosterolemia Situs Inversus Spiradenoma Splenic Abscess Splenic Infarction Splenic Sequestration Splenomegaly Split Hand Spondylocarpotarsal Synostosis Syndrome Spondyloocular Syndrome Spotted Fever Squamous Cell Carcinoma Subacute Bacterial Endocarditis Swine Influenza Synostosis Syphilis Systemic Lupus Erythematosus Tafro Syndrome Tay-Sachs Disease T-Cell Leukemia Testicular Germ Cell Cancer Tetanus Tetralogy of Fallot Thalassemia Three M Syndrome 1 Thrombasthenia Thrombocythemia 1 Thrombocytopenia 1 Thrombocytopenia 2 Thrombocytopenia 3 Thrombocytopenia 4 Thrombocytopenia-Absent Radius Syndrome Thrombocytopenia, Cyclic Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenia, Paris-Trousseau Type Thrombocytopenia Robin Sequence Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombosis Thrombotic Thrombocytopenic Purpura Thymic Hyperplasia Thymoma Thyroiditis Tibial Hemimelia Tick-Borne Encephalitis Timothy Syndrome Tonsillitis Townes-Brocks Syndrome Transient Global Amnesia Transmitted_by Transposition of the Great Arteries Tropical Sprue Tuberous Sclerosis 1 Tuberous Sclerosis 2 Typhoid Fever Ulcerative Colitis Uremia Van Der Woude Syndrome 1 Vascular Disease Vascular Hemostatic Disease Vasculitis Velocardiofacial Syndrome Ventricular Septal Defect Viral Hemorrhagic Fever Viral Hepatitis Virus-Associated Trichodysplasia Spinulosa Vitamin E, Familial Isolated Deficiency of Von Willebrand's Disease Wandering Spleen Wild Type Attr Amyloidosis Wilms Tumor 6 Wilson Disease Wiskott-Aldrich Syndrome Wyburn Mason's Syndrome Xanthogranulomatous Pyelonephritis Xanthomatosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome