Informaţii despre

Nume Homocystinuria
Pagina Web www.malacards.org
Clasificare globală Malacards Boli metabolice; Boli rare
Boli din aceeaşi familie Homocystinuria Due to Defect in Methylation Cbl E; Homocystinuria Due to Defect in Methylation Cbl G

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Boli A-Z Acute Liver Failure Acute Pancreatitis Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Amino Acid Metabolic Disorder Aminoaciduria Aneurysm Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Argininemia Arteries, Anomalies of Arteriosclerosis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Blood Group--Ahonen Blood Group, I System Blood Protein Disease Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brittle Bone Disorder Budd-Chiari Syndrome Bursitis Capgras Syndrome Carotid Artery Occlusion Cataract Cavernous Sinus Thrombosis Central Retinal Artery Occlusion Central Retinal Vein Occlusion Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Charles Bonnet Syndrome Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chronic Thromboembolic Pulmonary Hypertension Cleft Larynx, Posterior Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Congenital Hypothyroidism Conjunctivitis Cryofibrinogenemia Cryoglobulinemia Cystathioninuria Cystinuria Dementia Dwarfism Dystonia Endotheliitis Factor Vii Deficiency Factor Xii Deficiency Fibromuscular Dysplasia Galactosemia Glutamate Formiminotransferase Deficiency Glycine N-Methyltransferase Deficiency Hellp Syndrome Hemiplegia Hemolytic-Uremic Syndrome Hepatitis Homocysteinemia Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency Homocystinuria Due to Cystathionine Beta-Synthase Deficiency Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type Homocystinuria Without Methylmalonic Aciduria Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hyperlucent Lung Hypermethioninemia Hyperphenylalaninemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypomelanotic Disorder Hypotonia-Cystinuria Syndrome Inferior Vena Cava Interruption Inherited Metabolic Disorder Intracranial Hypertension Intracranial Thrombosis Iritis Ischemic Optic Neuropathy Isolated Ectopia Lentis Lens Subluxation Livedoid Vasculopathy Macrocytic Anemia Maple Syrup Urine Disease Marfan Syndrome Megaloblastic Anemia Methionine Adenosyltransferase I/iii Deficiency Methylmalonic Acidemia with Homocystinuria Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Moebius Syndrome Molybdenum Cofactor Deficiency Monoclonal Mast Cell Activation Syndrome Myelomeningocele Myopia Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurofibromatosis, Type Iv, of Riccardi Neuropathy Nonarteritic Anterior Ischemic Optic Neuropathy Nondisjunction Orotic Aciduria Pancreatitis Pancytopenia Patent Foramen Ovale Phacolytic Glaucoma Phenylketonuria Placenta Disease Placental Abruption Pneumothorax Porencephaly Portal Vein Thrombosis Pre-Eclampsia Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Pulmonary Hypertension Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis Retinal Artery Occlusion Retinal Degeneration Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Schizophrenia Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Sickle Cell Anemia Sneddon Syndrome Spinal Cord Infarction Spinal Cord Injury Sticky Platelet Syndrome Stroke, Ischemic Sudden Sensorineural Hearing Loss Three M Syndrome 1 Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Transcobalamin Ii Deficiency Transsexualism Transsexuality Trimethylaminuria Urea Cycle Disorder Varicose Veins Vascular Disease Vein Disease Ventricular Septal Defect Vitamin B12 Deficiency Vitamin Metabolic Disorder