Informaţii despre

Nume Glanzmann Thrombasthenia
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificari ICD10 Qualitative platelet defects
Clasificare anatomică Malacards Blood diseases

Vezi şi

Boli A-Z Acquired Hemophilia Acquired Hemophilia a Acquired Von Willebrand Syndrome Acute Myocardial Infarction Adie Pupil Afibrinogenemia Afibrinogenemia, Congenital Aging Alcohol-Related Birth Defect Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Autoimmune Disease of Blood Autosomal Dominant Macrothrombocytopenia Bernard-Soulier Syndrome Bleeding Disorder, Platelet-Type, 11 Bleeding Disorder, Platelet-Type, 16 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Cardiac Tamponade Carotid Artery Thrombosis Cerebral Falx Meningioma Cerebral Sinovenous Thrombosis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Thrombosis Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Disseminated Intravascular Coagulation Enterocele Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fainting Fetal and Neonatal Alloimmune Thrombocytopenia Fournier Gangrene Genitopatellar Syndrome Gilles De La Tourette Syndrome Gingivitis Gray Platelet Syndrome Hemarthrosis Hematopoietic Stem Cell Transplantation Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatitis Immune Suppression Immune System Disease Infective Endocarditis Inherited Blood Coagulation Disease Intermediate Coronary Syndrome Intermittent Claudication Intestinal Impaction Intracranial Thrombosis Ischemic Optic Neuropathy Korean Hemorrhagic Fever Leukemia Leukocyte Adhesion Deficiency, Type Iii Lymphoma Mild Hemophilia a Myeloid Leukemia Platelet Aggregation, Spontaneous Primary Ciliary Dyskinesia Primary Thrombocytopenia Prinzmetal's Variant Angina Protein S Deficiency Prothrombin Deficiency Pseudo-Von Willebrand Disease Pulmonary Embolism Purpura Purpura Fulminans Qualitative Platelet Defect Sagittal Sinus Thrombosis Severe Hemophilia a Severe Hemophilia B Stroke, Ischemic Sudden Sensorineural Hearing Loss Sveinsson Chorioretinal Atrophy Tetraamelia Syndrome, Autosomal Recessive Thrombasthenia Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombosis Thrombotic Thrombocytopenic Purpura Vein Disease Venous Insufficiency Ventricular Septal Defect Vitamin K Deficiency Hemorrhagic Disease Von Willebrand's Disease Von Willebrand Disease, Type 1 Von Willebrand Disease, Type 2 Von Willebrand Disease, Type 3