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Nume Thrombophilia Due to Thrombin Defect
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Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli de sânge
Boli din aceeaşi familie Thrombophilia Due to Activated Protein C Resistance; Thrombophilia Due to Thrombomodulin Defect; Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator

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Boli A-Z Abdominal Tuberculosis Acanthamoeba Keratitis Acquired Angioedema Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acrocallosal Syndrome Acute Leukemia Acute Liver Failure Acute Lymphocytic Leukemia Acute Myocardial Infarction Acute Necrotizing Encephalopathy Acute Pancreatitis Acute Respiratory Distress Syndrome Afibrinogenemia Afibrinogenemia, Congenital Aging Agraphia Alcoholic Liver Cirrhosis Alcohol-Related Birth Defect Alexia 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 Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Aneurysm Angina Pectoris Angioedema Angioedema, Hereditary, Type Iii Angiolipoma Angiomyolipoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Aplastic Anemia Appendicitis Argentine Hemorrhagic Fever Arteries, Anomalies of Arteriovenous Fistula Arteriovenous Malformation Arteritic Anterior Ischemic Optic Neuropathy Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 2a Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atrophic Gastritis Autoimmune Disease Autoimmune Enteropathy Bernard-Soulier Syndrome Bilateral Massive Adrenal Hemorrhage 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 Brain Injury Branch Retinal Artery Occlusion Breast Cancer Breast Reconstruction Budd-Chiari Syndrome Buerger Disease Burns Cardiac Arrest Cardiac Tamponade Carotid Artery Occlusion Carotid Artery Thrombosis Catastrophic Antiphospholipid Syndrome Cellulitis Central Retinal Vein Occlusion Central Serous Chorioretinopathy Cerebral Arteritis Cerebral Falx Meningioma Cerebral Palsy Cerebral Palsy, Ataxic, Autosomal Recessive Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Cervicitis Charles Bonnet Syndrome Chickenpox Choriocarcinoma Chronic Venous Insufficiency Churg-Strauss Syndrome Cicatricial Pemphigoid Cluster Headache Cocaine Abuse Coccidioidomycosis Colitis Collagen Disease Collecting Duct Carcinoma Colorectal Cancer Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Constrictive Pericarditis Coronary Thrombosis Cortical Blindness Cough Headache Cranial Nerve Palsy Craniofacial-Deafness-Hand Syndrome Craniopharyngioma Crouzon Syndrome Cryoglobulinemia Cryptogenic Cirrhosis Cutaneous Lupus Erythematosus Cystadenoma Cystic Fibrosis Cytochrome P450 2d6 Variant Cytomegalovirus Infection Dermatitis Dermatomyositis Developmental Dysplasia of the Hip 1 Diabetic Angiopathy Differentiated Thyroid Carcinoma Diffuse Lymphatic Malformation Discitis Disseminated Intravascular Coagulation Double Inferior Vena Cava Duodenitis Dysfibrinogenemia Eclampsia Eisenmenger Syndrome Encephalopathy Encephalopathy, Familial, with Neuroserpin Inclusion Bodies Endocarditis Endotheliitis Erdheim-Chester Disease Erysipelas Essential Thrombocythemia Ethmoid Sinusitis Exostosis Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor V and Factor Viii, Combined Deficiency of, 2 Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor V Leiden Thrombophilia Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Fasciitis Fibrinolytic Defect Fibromatosis Fournier Gangrene Frontal Sinusitis Gapo Syndrome Gastritis Giant Hemangioma Glanzmann Thrombasthenia Glioblastoma Glioblastoma Multiforme Glomerulonephritis Graves' Disease Hansen's Disease Hantavirus Pulmonary Syndrome Headache Hellp Syndrome Hemarthrosis Hemicrania Continua Hemoglobin E Disease Hemoglobinuria Hemolytic Anemia Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin Cofactor Ii Deficiency Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatocellular Carcinoma Hepatoportal Sclerosis Hereditary Spherocytosis Herpes Simplex Homocysteinemia Homocystinuria Hughes-Stovin Syndrome Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypopituitarism Hypotonia Idiopathic Scoliosis Ileocolitis Immune System Disease Immunodeficiency, Common Variable, 10 Immunoglobulin E Concentration, Serum Infective Endocarditis Inferior Vena Cava Interruption Inflammatory Bowel Disease Influenza Inherited Blood Coagulation Disease Intermediate Coronary Syndrome Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Hypotension Intracranial Sinus Thrombosis Intracranial Thrombosis Ischemia Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Korean Hemorrhagic Fever Laryngeal Adductor Paralysis Leech Infestation Legg-Calve-Perthes Disease Leiomyomatosis Leiomyosarcoma Lemierre's Syndrome Leukemia Liposarcoma Livedoid Vasculopathy Liver Cirrhosis Lung Cancer Lupus Erythematosus Lymphadenitis Lymphangitis Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Malignant Peripheral Nerve Sheath Tumor Marantic Endocarditis Mastoiditis May-Thurner Syndrome Megacolon Membranous Nephropathy Meningitis Meningococcemia Meningoencephalitis Mercury Poisoning Mesenteric Vascular Occlusion Microscopic Polyangiitis Mild Hemophilia a Mixed-Type Autoimmune Hemolytic Anemia Mucositis Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly Multiple Cranial Nerve Palsy Multiple Sclerosis Mungan Syndrome Mutism Myeloid Leukemia Myelomeningocele Myeloproliferative Neoplasm Myhre Syndrome Myocardial Infarction Myoma Neonatal Stroke Nephrotic Syndrome Neuroblastoma Neuropathy Neuroretinitis Neurosarcoidosis Neutropenia Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Hydrocephalus Oligodendroglioma Osteochondroma Osteomyelitis Osteonecrosis Ovarian Cancer Ovarian Hyperstimulation Syndrome Paine Syndrome Pancreatitis Panniculitis Panuveitis Papilledema Paracetamol Poisoning Paralytic Ileus Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Pemphigus Pemphigus Vegetans Pemphigus Vulgaris Pericarditis Peripheral Artery Disease Peripheral Vascular Disease Peripheral Vertigo Peritonitis Pernicious Anemia Petrositis Pheochromocytoma Pilocytic Astrocytoma Piriformis Syndrome Placenta Disease Placental Abruption Plasmacytoma Plasminogen Activator Inhibitor-1 Deficiency Platelet Aggregation, Spontaneous Pneumococcal Meningitis Pneumonia Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polymyositis Porencephaly Portal Hypertension Portal Vein Thrombosis Postaxial Acrofacial Dysostosis Post-Thrombotic Syndrome Prader-Willi Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Priapism Prostatitis Protein C Deficiency Protein-Losing Enteropathy Protein S Deficiency Protein Z Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Prothrombin-Related Thrombophilia Pseudohypoaldosteronism Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Hyalinizing Granuloma Pulmonary Tuberculosis Purpura Purpura Fulminans Pyomyositis Quadriplegia Qualitative Platelet Defect Quebec Platelet Disorder Radiculopathy Raynaud Disease Reflex Sympathetic Dystrophy Relapsing Polychondritis Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Retroperitoneal Fibrosis Reversible Cerebral Vasoconstriction Syndrome Sagittal Sinus Thrombosis Sapho Syndrome Sarcoma Sciatic Neuropathy Scoliosis Scott Syndrome Scrub Typhus Septic Arthritis Severe Hemophilia a Severe Pre-Eclampsia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwartzman Phenomenon Sinusitis Sleep Apnea Sneddon Syndrome Soft Tissue Sarcoma Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spinal Cord Infarction Spinal Cord Injury Spindle Cell Sarcoma Splenic Infarction Spontaneous Intracranial Hypotension Spotted Fever Status Epilepticus Sticky Platelet Syndrome Stroke, Ischemic Subdural Empyema Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Testicular Cancer Thoracic Outlet Syndrome Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombomodulin Defect Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator Thrombophlebitis Thrombophlebitis Migrans Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Toxic Megacolon Transient Global Amnesia Transsexualism Transsexuality Traumatic Brain Injury Tuberculous Meningitis Ulcerative Colitis Undifferentiated Pleomorphic Sarcoma Unilateral Absence of a Pulmonary Artery Vaginitis Valproate Embryopathy Varicose Veins Vascular Disease Vasculitis Vein Disease Venous Insufficiency Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3 Wandering Spleen