Bilirubin Metabolic Disorder

Informaţii despre

Nume		Bilirubin Metabolic Disorder
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli metabolice
Clasificari ICD10		Other disorders of bilirubin metabolism

Vezi şi

Boli A-Z		Abdominal Tuberculosis Acute Liver Failure Adenocarcinoma Adenosine Deaminase Deficiency Aging Alcoholic Hepatitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alpha-Thalassemia Al-Raqad Syndrome Analbuminemia Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Aniridia 1 Anorexia Nervosa 1 Antipyrine Metabolism Aplastic Anemia Appendicitis Arthrochalasia Ehlers-Danlos Syndrome Asphyxiating Thoracic Dystrophy Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autoimmune Hepatitis Beta-Thalassemia Bile Duct Cysts Bile Duct Disease Biliary Atresia Biliary Tract Disease Blackwater Fever Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group Incompatibility Blood Group, I System Brainstem Auditory Evoked Responses Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cerebellar Hypoplasia Cerebral Palsy Cerebritis Childhood Leukemia Cholangitis Cholecystitis Choledocholithiasis Cholelithiasis Cholestasis Chromhidrosis Cleidocranial Dysplasia Congenital Hemolytic Anemia Congenital Hypothyroidism Constrictive Pericarditis Crigler-Najjar Syndrome, Type I Crigler-Najjar Syndrome, Type Ii Crimean-Congo Hemorrhagic Fever Descending Colon Cancer Dihydropyrimidine Dehydrogenase Deficiency Dubin-Johnson Syndrome Duodenal Atresia Duodenitis Eclampsia Encephalopathy Endotheliitis Epilepsy Esophageal Cancer Evans' Syndrome Extrahepatic Cholestasis Extrinsic Allergic Alveolitis Factor Xi Deficiency Febrile Seizures Fournier Gangrene Galactosemia Gallbladder Disease Gilbert Syndrome Glucosephosphate Dehydrogenase Deficiency Glucose Phosphate Isomerase Deficiency Glutathione Peroxidase Deficiency Glutathione Synthetase Deficiency Hellp Syndrome Heme Oxygenase 1 Deficiency Hemoglobin H Disease Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemorrhagic Disease Hemorrhagic Fever Hepatic Coma Hepatic Encephalopathy Hepatic Tuberculosis Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatitis B Hepatitis D Hepatitis E Hepatoportal Sclerosis Hepatorenal Syndrome Hereditary Spherocytosis Hyperbilirubinemia, Rotor Type Hyperbiliverdinemia Hyper Ige Syndrome Hyperphosphatemia Hyperthyroidism Hypertrophic Pyloric Stenosis Hypoglycemia Hypopituitarism Inherited Metabolic Disorder Intracranial Embolism Intrahepatic Cholestasis Irinotecan Toxicity Kernicterus Koro Kwashiorkor Leptospirosis Leukemia Leukomalacia Liver Cirrhosis Liver Disease Mastitis Methemoglobinemia Myeloid Leukemia Neonatal Jaundice Neonatal Thyrotoxicosis Neuronitis Neuropathy Non-a-E Hepatitis Obstructive Jaundice Pancreatitis Parametritis Parotitis Paroxysmal Nocturnal Hemoglobinuria Pericarditis Periventricular Leukomalacia Pigmentation Disease Porphyria Portal Hypertension Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Purpura Pyloric Stenosis Pyruvate Kinase Deficiency of Red Cells Q Fever Retinal Artery Occlusion Schizophrenia Senile Cataract Sensorineural Hearing Loss Severe Combined Immunodeficiency Short Bowel Syndrome Sickle Cell Anemia Testicular Regression Syndrome Thalassemia Thrombocytopenia Thrombotic Thrombocytopenic Purpura Thrombotic Thrombocytopenic Purpura, Congenital Viral Hepatitis Wilson Disease X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome