Informaţii despre

Nume Sneddon Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Rare diseases
Clasificari ICD10 Other specified disorders of arteries and arterioles
Clasificare anatomică Malacards Bone diseases; Cardiovascular diseases; Neuronal diseases; Skin diseases

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Boli A-Z Acanthamoeba Keratitis Acute Liver Failure Adenosine Deaminase 2 Deficiency Afibrinogenemia Afibrinogenemia, Congenital 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 Al-Raqad Syndrome Angiomatosis Aniridia 1 Anorexia Nervosa 1 Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Arthrochalasia Ehlers-Danlos Syndrome Autoimmune Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Carotid Artery Occlusion Catastrophic Antiphospholipid Syndrome Central Nervous System Origin Vertigo Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cranial Nerve Palsy Cryptogenic Cirrhosis Dementia Disseminated Intravascular Coagulation Dysfibrinogenemia Encephalopathy Endocarditis Esophageal Varix Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Fournier Gangrene Giant Hemangioma Haim-Munk Syndrome Headache Hellp Syndrome Hemoglobin E Disease Hemophilia B Hemorrhagic Disease Hepatic Infarction Hepatitis a Homocysteinemia Homocystinuria Hypersplenism Immune System Disease Inherited Blood Coagulation Disease Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Ischemic Optic Neuropathy Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Livedoid Vasculopathy Lupus Erythematosus Marantic Endocarditis May-Thurner Syndrome Meningococcemia Mini Stroke Nonarteritic Anterior Ischemic Optic Neuropathy Papilledema Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Polyarteritis Nodosa Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Purpura Fulminans Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Scott Syndrome Severe Pre-Eclampsia Spinal Cord Disease Spinal Cord Infarction Splenic Infarction Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Transient Global Amnesia Varicose Veins Vasculitis Vein Disease Von Willebrand's Disease