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Pancytopenia
Informaţii despre
Nume
Pancytopenia
Pagina Web
www.malacards.org
Clasificare anatomică Malacards
Boli de sânge
Vezi şi
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
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