Informaţii despre

Nume Wilson Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Disorders of copper metabolism
Clasificare anatomică Malacards Boli ale ochiului; Boli gastrointestinale; Boli hepatice; Boli nefrologice (ale rinichilor); Boli neuronale

Vezi şi

Boli A-Z Abdominal Tuberculosis Aceruloplasminemia Acute Liver Failure Acute Respiratory Distress Syndrome Aging Akinetic Mutism Alagille Syndrome 1 Alcohol Abuse Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amenorrhea Analbuminemia Aniridia 1 Anorexia Nervosa 1 Antipyrine Metabolism Arthritis Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Atransferrinemia Beta-Thalassemia Bilirubin Metabolic Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Bornholm Eye Disease Brainstem Auditory Evoked Responses Bullous Pemphigoid Cataract Cavernous Malformation Central Pontine Myelinolysis Cerebral Cavernous Malformations Cerebral Degeneration Cerebritis Cholangitis Cholecystitis Choledocholithiasis Cholestasis Citrullinemia, Classic Cleft Palate, Isolated Crescentic Glomerulonephritis Crouzon Syndrome with Acanthosis Nigricans Cystic Fibrosis Dermatitis Dysphagia Dystonia Elastosis Perforans Serpiginosa Encephalopathy Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Epidermolytic Hyperkeratosis Epilepsy Epstein-Barr Virus Hepatitis Erythermalgia, Primary Fanconi Anemia, Complementation Group E Fascioliasis Focal Dystonia Fontaine Progeroid Syndrome Fournier Gangrene Glomerulonephritis Growth Hormone Deficiency Hemochromatosis, Type 1 Hemoglobin E-Beta-Thalassemia Syndrome Hemolytic Anemia Hemorrhagic Fever Hemosiderosis Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatic Tuberculosis Hepatitis Hepatitis a Hepatitis B Hepatitis D Hepatitis E Hepatocellular Carcinoma Hepatoportal Sclerosis Huntington Disease Hyperferritinemia with or Without Cataract Hypertrophic Olivary Degeneration Hypochromic Microcytic Anemia Hypogonadism Hypopituitarism Iga Glomerulonephritis Immune System Disease Infertility Influenza Inherited Metabolic Disorder Intrahepatic Cholestasis Iron Metabolism Disease Iron Overload in Africa Kwashiorkor Laryngeal Adductor Paralysis Leishmaniasis Leukemia Lipomatosis Liver Cirrhosis Liver Disease Luscan-Lumish Syndrome Lymphoblastic Leukemia Marasmus Meningitis and Encephalitis Menkes Disease Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma Metal Metabolism Disorder Mineral Metabolism Disease Mutism Myhre Syndrome Nephrocalcinosis Neurofibromatosis, Type Iv, of Riccardi Neuropathy Non-a-E Hepatitis Nonalcoholic Steatohepatitis Obstructive Jaundice Occipital Horn Syndrome Orbital Cyst Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondritis Dissecans Pancreatitis, Hereditary Pandas Pemphigus Peritonitis Polyneuropathy Portal Hypertension Primary Cerebellar Degeneration Psoriasis Psoriasis 13 Pulmonary Fibrosis Purpura Pyoderma Pyoderma Gangrenosum Retinoblastoma Schizophrenia Seminoma Spinocerebellar Degeneration Spondyloocular Syndrome Swayback Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thrombocytopenia Thyroiditis Tibia, Hypoplasia or Aplasia of, with Polydactyly Tremor Undifferentiated Pleomorphic Sarcoma Viral Hepatitis Visceral Leishmaniasis