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Nume Homocysteinemia
Pagina Web www.malacards.org
Clasificare globală Malacards Metabolic diseases; Rare diseases

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Boli A-Z Abdominal Tuberculosis Acquired Angioedema Acute Liver Failure Acute Myocardial Infarction Acute Posterior Multifocal Placoid Pigment Epitheliopathy Afibrinogenemia, Congenital Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Plasmin Inhibitor Deficiency Al-Raqad Syndrome Amaurosis Fugax Amino Acid Metabolic Disorder Analbuminemia Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antipyrine Metabolism Antithrombin Iii Deficiency Argentine Hemorrhagic Fever Arteries, Anomalies of Arteriosclerosis Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Blood Coagulation Disease Blood Group--Ahonen 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 Branch Retinal Artery Occlusion Budd-Chiari Syndrome Buerger Disease Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Charles Bonnet Syndrome Cholangitis Colorectal Adenoma Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Coronary Artery Anomaly Coronary Stenosis Cryptogenic Cirrhosis Dementia Diabetes Mellitus Disseminated Intravascular Coagulation Down Syndrome Dysfibrinogenemia Eclampsia Endocarditis Endotheliitis Esophageal Varix Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Fibrinolytic Defect Fournier Gangrene Giant Hemangioma Glycine N-Methyltransferase Deficiency Hellp Syndrome Hemifacial Spasm Hemoglobin E Disease Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Hepatic Coma Hepatic Infarction Hepatic Tuberculosis Hepatic Vascular Disease Hepatitis Hepatitis a Hepatitis C Hepatitis C Virus Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypermethioninemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Immune System Disease Infective Endocarditis Inferior Vena Cava Interruption Inflammatory Bowel Disease Inherited Metabolic Disorder Intermittent Claudication Intestinal Impaction Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Ischemic Heart Disease Ischemic Neuropathy Ischemic Optic Neuropathy Isolated Ectopia Lentis Kwashiorkor Leech Infestation Legg-Calve-Perthes Disease Lemierre's Syndrome Lens Subluxation Livedoid Vasculopathy Liver Cirrhosis Lung Disease Lupus Erythematosus Malignant Otitis Externa Marantic Endocarditis Mastoiditis Mediastinitis Megaloblastic Anemia Meningococcemia Mesenteric Vascular Occlusion Methionine Adenosyltransferase I/iii Deficiency Methotrexate Toxicity or Dose Selection Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria, Cblf Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Microvascular Complications of Diabetes 5 Monoclonal Mast Cell Activation Syndrome Multiple Sclerosis Myelomeningocele Myocardial Infarction Neonatal Stroke Neural Tube Defects Neural Tube Defects, Folate-Sensitive Non-a-E Hepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Nondisjunction Nutritional Deficiency Disease Osteonecrosis Paracetamol Poisoning Patent Foramen Ovale Pediatric Osteosarcoma Peripheral Vertigo Peritonitis Placenta Disease Placental Abruption Placental Choriocarcinoma Polycystic Ovary Syndrome Porencephaly Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Pregnancy Loss, Recurrent 1 Priapism Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Edema Pulmonary Embolism Purpura Purpura Fulminans Pyuria Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Sagittal Sinus Thrombosis Schizophrenia Severe Pre-Eclampsia Sneddon Syndrome Spinal Cord Infarction Sticky Platelet Syndrome Stroke, Ischemic Subclavian Steal Syndrome Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Thrombasthenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Transcobalamin Ii Deficiency Varicose Veins Vascular Disease Vasculitis Vein Disease Venous Insufficiency Vitamin B12 Deficiency Vitamin Metabolic Disorder