Informaţii despre

Nume Antiphospholipid Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale sistemului imunitar
Boli din aceeaşi familie Antiphospholipid Syndrome, Familial

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Boli A-Z Acalculous Cholecystitis Acanthamoeba Keratitis Acquired Angioedema Acquired Hemophilia Acquired Hemophilia a Acromegaloid Facial Appearance Syndrome Acute Adrenal Insufficiency Acute Interstitial Pneumonia Acute Myocardial Infarction Acute Pancreatitis Acute Promyelocytic Leukemia Acute Respiratory Distress Syndrome Adenosine Deaminase 2 Deficiency Adult Respiratory Distress Syndrome Afibrinogenemia Afibrinogenemia, Congenital African Tick-Bite Fever Aging Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha Chain Disease Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Aneurysm Angina Pectoris Angioedema Angioimmunoblastic T-Cell Lymphoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome, Familial Antithrombin Iii Deficiency Aortic Aneurysm Aortic Valve Disease 2 Aortitis Aplasia Cutis Congenita Aplastic Anemia Apparent Mineralocorticoid Excess Argentine Hemorrhagic Fever Arteries, Anomalies of Arteriosclerosis Arteriovenous Fistula Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Aspergillosis Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atrial Septal Aneurysm Atrichia with Papular Lesions Autism Autism Spectrum Disorder Autoimmune Disease Autoimmune Disease of Blood Autoimmune Hepatitis Autonomic Dysfunction Axillary Adenitis Bacterial Conjunctivitis Banti's Syndrome Bilateral Massive Adrenal Hemorrhage Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome 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 Necrosis Borderline Leprosy Bornholm Eye Disease Boutonneuse Fever Branch Retinal Artery Occlusion Brill-Zinsser Disease Budd-Chiari Syndrome Buerger Disease C1 Inhibitor Deficiency C1q Nephropathy Cardiac Tamponade Cardiac Valvular Defect, Developmental Cardiogenic Shock Carotid Artery Dissection Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Cd40 Ligand Deficiency Central Retinal Artery Occlusion Central Retinal Vein Occlusion Central Serous Chorioretinopathy Cerebral Atrophy Cerebral Falx Meningioma Cerebral Hemorrhage Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Chikungunya Cholangitis Cholecystitis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Choroiditis Chromosomal Triplication Chronic Graft Versus Host Disease Chronic Interstitial Cystitis Chronic Myelomonocytic Leukemia Chronic Thromboembolic Pulmonary Hypertension Cocaine Abuse Cold Agglutinin Disease Colitis Complement Component 4, Partial Deficiency of Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Dyserythropoietic Anemia Congenital Syphilis Congenital Toxoplasmosis Conjunctivitis Connective Tissue Disease Cork-Handlers' Disease Coronary Arterial Fistulas Coronary Artery Dissection, Spontaneous Coronary Stenosis Coronary Thrombosis Cortical Blindness Corticobasal Degeneration Cranial Nerve Palsy Crescentic Glomerulonephritis Crouzon Syndrome with Acanthosis Nigricans Cryofibrinogenemia Cryoglobulinemia Cryptogenic Cirrhosis Cutaneous Lupus Erythematosus Cysticercosis Dementia Dengue Hemorrhagic Fever Dermatitis Dermatomyositis Diabetic Angiopathy Diffuse Alveolar Hemorrhage Digeorge Syndrome Dilated Cardiomyopathy Diphtheria Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Down Syndrome Dysfibrinogenemia Dysgammaglobulinemia Early Yaws Eclampsia Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Endocardium Disease Endometrial Cancer Endomyocardial Fibrosis Endotheliitis Epilepsy Erythema Infectiosum Erythema Multiforme Evans' Syndrome Exudative Glomerulonephritis Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fallopian Tube Disease Fasciitis Fascioliasis Fibrinolytic Defect Fibromuscular Dysplasia Focal Segmental Glomerulosclerosis Fournier Gangrene Galactose Epimerase Deficiency Gastroduodenitis Geniculate Herpes Zoster Giant Hemangioma Gilles De La Tourette Syndrome Glanzmann Thrombasthenia Glomerulonephritis Graft-Versus-Host Disease Granulomatous Dermatitis Growth Control, Y-Chromosome Influenced Hairy Cell Leukemia Hansen's Disease Hantavirus Pulmonary Syndrome Headache Heart Valve Disease Heavy Chain Disease Hellp Syndrome Hematopoietic Stem Cell Transplantation Hemoglobin E Disease Hemoglobinuria Hemolytic Anemia Hemolytic-Uremic Syndrome Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus Hepatitis D Hereditary Hemorrhagic Telangiectasia Herpes Simplex Heterophyiasis Histiocytosis Homocysteinemia Homocystinuria Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglobulinemic Purpura Hypersensitivity Reaction Disease Hypersensitivity Reaction Type Iii Disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoadrenalism Hypopituitarism Immune System Disease Immunoglobulin a Deficiency 1 Immunoglobulin Alpha Deficiency Immunoglobulin G Deficiency Inferior Myocardial Infarction Inferior Vena Cava Interruption Influenza Inherited Blood Coagulation Disease Insulin-Like Growth Factor I Intermittent Claudication Intestinal Impaction Intestinal Perforation Intracranial Embolism Intracranial Hypertension Intracranial Sinus Thrombosis Intracranial Thrombosis Invasive Aspergillosis Ischemia Ischemic Colitis Ischemic Optic Neuropathy Ischemic Retinopathy Kidney Cortex Necrosis Korean Hemorrhagic Fever Langerhans Cell Histiocytosis Lateral Sinus Thrombosis Leech Infestation Legg-Calve-Perthes Disease Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Limb Ischemia Lipodystrophy, Partial, Acquired Lipoid Proteinosis of Urbach and Wiethe Livedoid Vasculopathy Liver Cirrhosis Localized Scleroderma Locked-in Syndrome Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphoblastic Leukemia Lymphoid Interstitial Pneumonia Lymphoma Macrophage Activation Syndrome Malignant Hypertension Marantic Endocarditis Maxillary Sinusitis May-Thurner Syndrome Melanoma Membranous Nephropathy Meningitis Meningococcemia Meningovascular Neurosyphilis Mercury Poisoning Mesenteric Vascular Occlusion Microscopic Polyangiitis Middle Cerebral Artery Infarction Mixed Connective Tissue Disease Monoclonal Paraproteinemia Mononeuropathy Mucopolysaccharidosis, Type Vii Musical Perfect Pitch Myasthenia Gravis Mycosis Fungoides Myelitis Myeloproliferative Neoplasm Myocardial Infarction Myocarditis Myoclonus Myositis Neonatal Antiphospholipid Syndrome Neovascular Glaucoma Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neuroretinitis Nodular Regenerative Hyperplasia Nonarteritic Anterior Ischemic Optic Neuropathy Ophthalmia Neonatorum Optic Nerve Disease Orbital Granuloma Osteonecrosis Palindromic Rheumatism Pancreatitis Pancytopenia Panniculitis Papilledema Paracetamol Poisoning Parotid Disease Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Pauci-Immune Glomerulonephritis Pdgfrb-Associated Chronic Eosinophilic Leukemia Pediatric Systemic Lupus Erythematosus Peripheral Artery Disease Peripheral Vascular Disease Peripheral Vertigo Peritonitis Pigmented Purpuric Dermatosis Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Placenta Disease Placental Abruption Platelet Aggregation, Spontaneous Pleuropneumonia Pneumonia Polyarteritis Nodosa Polyclonal Hypergammaglobulinemia Polymyositis Porencephaly Portal Hypertension Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Priapism Primary Anetoderma Primary Biliary Cirrhosis Primary Thrombocytopenia Proliferative Glomerulonephritis Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pseudobulbar Palsy Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Pulmonary Sarcoidosis Pure Red-Cell Aplasia Purpura Purpura Fulminans Pustulosis Palmaris Et Plantaris Pyoderma Pyoderma Gangrenosum Q Fever Qualitative Platelet Defect Quebec Platelet Disorder Reactive Angioendotheliomatosis Reflex Sympathetic Dystrophy Relapsing Polychondritis Renovascular Hypertension Retinal Artery Occlusion Retinal Ischemia Retinal Vascular Occlusion Retinal Vasculitis Retinal Vein Occlusion Retinitis Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatoid Arthritis Sagittal Sinus Thrombosis Salpingitis Salpingo-Oophoritis Sapho Syndrome Sarcoidosis 2 Schistosomiasis Scleritis Sclerosing Cholangitis Scott Syndrome Selective Igg Deficiency Disease Selective Immunoglobulin Deficiency Disease Sensorineural Hearing Loss Severe Hemophilia a Severe Pre-Eclampsia Shwartzman Phenomenon Sickle Cell Anemia Silent Myocardial Infarction Situs Inversus Sneddon Syndrome Spinal Cord Infarction Spinocerebellar Ataxia, Autosomal Recessive 10 Splenic Disease Splenic Infarction Splenomegaly Spondylitis Spondyloarthropathy 1 Spondyloocular Syndrome Status Epilepticus Sticky Platelet Syndrome Stroke, Ischemic Subacute Bacterial Endocarditis Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Syphilis Syphilitic Meningitis Systemic Lupus Erythematosus Systemic Scleroderma Takayasu Arteritis Testicular Torsion Tetanus Thrombasthenia Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Timothy Syndrome Transient Global Amnesia Transient Hypogammaglobulinemia of Infancy Transverse Myelitis Trichostrongyloidiasis Tricuspid Valve Disease Tuberous Sclerosis 1 Tuberous Sclerosis 2 Typhoid Fever Varicose Veins Vascular Disease Vasculitis Vein Disease Venous Insufficiency Ventilation Pneumonitis Viral Exanthem Virus-Associated Trichodysplasia Spinulosa Von Willebrand's Disease Von Willebrand Disease, Type 1