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Nume Pancytopenia
Pagina Web www.malacards.org
Clasificare anatomică Malacards Blood diseases

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Boli A-Z Aceruloplasminemia Acquired Von Willebrand Syndrome Acromelic Frontonasal Dysostosis Acute Graft Versus Host Disease Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Promyelocytic Leukemia Acute Transverse Myelitis Adenoma Adult Respiratory Distress Syndrome Adult T-Cell Leukemia Agammaglobulinemia Aging Alopecia Alopecia Totalis Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amegakaryocytic Thrombocytopenia, Congenital Anca-Associated Vasculitis Anemia of Prematurity Angiomatosis Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Aregenerative Anemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Ataxia-Pancytopenia Syndrome Atrial Fibrillation Babesiosis Bacillary Angiomatosis Back Pain Bardet-Biedl Syndrome B-Cell Lymphomas Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Bleeding Disorder, Platelet-Type, 14 Blood Group--Ahonen Blood Group, I System Bone Marrow Cancer Bone Marrow Necrosis Brain Small Vessel Disease with or Without Ocular Anomalies Breast Cancer Brucellosis Bullous Pemphigoid Capillary Leak Syndrome Catastrophic Antiphospholipid Syndrome Central Nervous System Lymphoma Cerebellar Hypoplasia Cerebral Hemorrhage Cerebritis Cholangitis Cholecystitis Cholestasis Chromosomal Triplication Chromosome 5q Deletion Syndrome Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hepatic Fibrosis Congenital Human Immunodeficiency Virus Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crohn's Colitis Crohn's Disease Cryoglobulinemia Cutaneous Sclerosis Cyclic Neutropenia Cystinosis Cytomegalovirus Infection Deficiency Anemia Dermatomyositis Diarrhea Diffuse Large B-Cell Lymphoma Digeorge Syndrome Disseminated Intravascular Coagulation Duodenitis Dyskeratosis Congenita Dyskeratosis Congenita Autosomal Dominant Dyskeratosis Congenita, Autosomal Dominant 6 Ehrlichiosis Endocarditis Engraftment Syndrome Erythema Elevatum Diutinum Essential Thrombocythemia Evans' Syndrome Exocrine Pancreatic Insufficiency Factitious Disorder Fanconi-Like Syndrome Fanconi Syndrome Felty Syndrome Folate Malabsorption, Hereditary Folic Acid Deficiency Anemia Gamma Heavy Chain Disease Gastroenteritis Glioblastoma Graft-Versus-Host Disease Granulomatous Myositis Granulosa Cell Tumor of the Ovary Graves' Disease Hairy Cell Leukemia Heavy Chain Disease Helicobacter Pylori Infection Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatoblastoma Hepatocellular Carcinoma Hereditary Spherocytosis Histoplasmosis Homocystinuria Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency Horseshoe Kidney Human Coronavirus Sensitivity Human Monocytic Ehrlichiosis Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hyperglycemia Hyperlipoproteinemia, Type Iv Hyperparathyroidism Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoglycemia Hypogonadism Hypopituitarism Immune System Disease Influenza Inherited Bone Marrow Failure Syndromes Intrahepatic Cholestasis Intravascular Large B-Cell Lymphoma Isovaleric Acidemia Johanson-Blizzard Syndrome Juvenile Xanthogranuloma Keratoacanthoma Lactic Acidosis Left Ventricular Noncompaction Leishmaniasis Leptospirosis Leukemia Lupus Erythematosus Lyme Disease Lymphoblastic Leukemia Lymphoma Lymphomatoid Granulomatosis Macrocytic Anemia Macroglobulinemia Malaria Megaloblastic Anemia Melanoma Meningoencephalitis Merkel Cell Carcinoma Microcephaly Miliary Tuberculosis Mosaic Trisomy 8 Mucopolysaccharidosis, Type Vii Mucositis Mycobacterium Kansasii Myelitis Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myopathy Myositis Neonatal Lupus Erythematosus Nephrotic Syndrome Neuromyelitis Optica Neuropathy Neutropenia Paget Disease, Extramammary Pancreatitis Paraganglioma Paraneoplastic Syndromes Paraplegia Paroxysmal Nocturnal Hemoglobinuria Pearson Marrow-Pancreas Syndrome Pelvic Inflammatory Disease Peripheral T-Cell Lymphoma Peritonitis Pernicious Anemia Phocomelia Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Plasmodium Vivax Malaria Pneumonia Pneumothorax Polyarteritis Nodosa Polycythemia Polycythemia Vera Polyneuropathy Pompholyx Portal Hypertension Portal Vein Thrombosis Primary Biliary Cirrhosis Primary Hyperoxaluria Primary Hyperparathyroidism Progressive Multifocal Leukoencephalopathy Propionic Acidemia Prostate Cancer Prostatitis Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Alveolar Proteinosis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Tuberculosis Pure Red-Cell Aplasia Pyoderma Pyoderma Gangrenosum Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Refractory Anemia Renal Osteodystrophy Retinitis Rheumatoid Arthritis Samd9l-Related Ataxia-Pancytopenia Syndrome Sarcoidosis 2 Schizophrenia Severe Combined Immunodeficiency Severe Congenital Neutropenia Sheehan Syndrome Shwachman-Diamond Syndrome Splenic Abscess Splenomegaly Spotted Fever Subacute Bacterial Endocarditis Systemic Lupus Erythematosus T-Cell Leukemia Thalassemia Thrombocythemia 1 Thrombocytopenia Thrombocytopenia 3 Thrombocytopenia Due to Platelet Alloimmunization Thrombocytosis Thrombosis Thymoma Thyroiditis Toxic Shock Syndrome Toxoplasmoză Transverse Myelitis Tuberculous Peritonitis Tuberous Sclerosis Ulcerative Colitis Vacterl Association Vasculitis Viral Hepatitis Visceral Leishmaniasis Vitamin B12 Deficiency Weber Syndrome Xanthomatosis