Informaţii despre

Nume Paroxysmal Nocturnal Hemoglobinuria
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Haemoglobinuria due to haemolysis from other external causes; Other autoimmune haemolytic anaemias; Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
Clasificare anatomică Malacards Boli ale sistemului imunitar; Boli de sânge; Boli nefrologice (ale rinichilor)
Boli din aceeaşi familie Paroxysmal Nocturnal Hemoglobinuria 1; Paroxysmal Nocturnal Hemoglobinuria 2

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acute Hemorrhagic Conjunctivitis Acute Kidney Tubular Necrosis Acute Leukemia Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Aging 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 Androgen Insensitivity Syndrome, Mild Anemia, Autoimmune Hemolytic Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aplastic Anemia Arthrochalasia Ehlers-Danlos Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bornholm Eye Disease Brain Small Vessel Disease with or Without Ocular Anomalies Budd-Chiari Syndrome Cardiomyopathy, Familial Hypertrophic, 1 Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebellar Degeneration-Related Autoantigen 3 Cerebritis Cholangitis Chronic Graft Versus Host Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Duodenal Obstruction Duodenitis Dystonia Encephalopathy Endotheliitis End Stage Renal Failure Eosinophilic Fasciitis Extrinsic Allergic Alveolitis Fanconi Syndrome Fasciitis Glucose Phosphate Isomerase Deficiency Glycosylphosphatidylinositol Deficiency Graft-Versus-Host Disease Hematopoietic Stem Cell Transplantation Hemoglobinuria Hemolytic Anemia Hemolytic Anemia, Cd59-Mediated, with or Without Immune-Mediated Polyneuropathy Hemolytic-Uremic Syndrome Hemosiderosis Heparin-Induced Thrombocytopenia Hepatic Encephalopathy Hepatitis Hereditary Spherocytosis Hereditary Wilms' Tumor Hypercoagulability Syndrome Due to Glycosylphosphatidylinositol Deficiency Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Inherited Bone Marrow Failure Syndromes Interstitial Nephritis Intestinal Perforation Intracranial Embolism Ischemia Lactic Acidosis Large Granular Lymphocyte Leukemia Leukemia Localized Scleroderma Lupus Erythematosus Lymphoblastic Leukemia Lymphocytes Absent Lymphoma Lymphoplasmacytic Lymphoma Mirage Syndrome Monocytic Leukemia Moyamoya Disease 1 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 Mycobacterium Kansasii Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloma, Multiple Myeloproliferative Neoplasm Myocardial Infarction Necrobiotic Xanthogranuloma Necrotizing Fasciitis Neutropenia Non-a-E Hepatitis Non-Involuting Congenital Hemangioma Obstructive Jaundice Osteomyelitis Pancreatitis, Hereditary Pancytopenia Papilledema Papillon-Lefevre Syndrome Paroxysmal Nocturnal Hemoglobinuria 1 Patent Foramen Ovale Perforated Corneal Ulcer Plasminogen Deficiency, Type I Portal Hypertension Portal Vein Thrombosis Posttransplant Acute Limbic Encephalitis Potocki-Lupski Syndrome Primary Lateral Sclerosis, Adult, 1 Properdin Deficiency Properdin Deficiency, X-Linked Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Purpura Refractory Anemia Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Sickle Cell Disease Siderosis Spasticity Spastic Paraparesis Splenic Infarction Sveinsson Chorioretinal Atrophy Systemic Lupus Erythematosus Temporal Arteritis Thalassemia Thrombocytopenia Thrombocytosis Thrombosis Thrombotic Thrombocytopenic Purpura Thymoma Treacher Collins Syndrome 1 Tropical Spastic Paraparesis Ureter, Cancer of