Informaţii despre

Nume Cholestasis
Pagina Web www.malacards.org
Clasificari ICD10 Obstruction of bile duct
Clasificare anatomică Malacards Gastrointestinal diseases; Liver diseases

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Acth Deficiency, Isolated Acute Liver Failure Adenocarcinoma Agammaglobulinemia Aggressive Systemic Mastocytosis Aging Alagille Syndrome 1 Al Amyloidosis Alcoholic Hepatitis Alkaline Phosphatase, Plasma Level of, Quantitative Trait Locus 1 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 Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Amyloidosis Aniridia 1 Anorexia Nervosa 1 Anthracosilicosis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Atp8b1 Deficiency Autoimmune Hepatitis Autoimmune Pancreatitis Ayme-Gripp Syndrome Benign Idiopathic Neonatal Seizures Bile Acid Synthesis Defect, Congenital, 1 Bile Duct Disease Biliary Atresia Biliary Atresia, Extrahepatic Biliary Tract Disease Bilirubin Metabolic Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Bowen-Conradi Syndrome Breast Cancer Bronchopulmonary Dysplasia Brucellosis Cardiac Tamponade Cardiogenic Shock Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cerebrotendinous Xanthomatosis Cholangiocarcinoma Cholangitis Cholangitis, Primary Sclerosing Cholecystitis Choledocholithiasis Cholelithiasis Cholestasis, Benign Recurrent Intrahepatic, 1 Cholestasis, Benign Recurrent Intrahepatic, 2 Cholestasis-Lymphedema Syndrome Cholestasis, Progressive Familial Intrahepatic, 1 Cholestasis, Progressive Familial Intrahepatic, 2 Cholestasis, Progressive Familial Intrahepatic, 3 Chromosome Xp21 Deletion Syndrome Chronic Enteropathy Associated with Slco2a1 Gene Churg-Strauss Syndrome Ciliopathy Citrullinemia, Type Ii, Neonatal-Onset Cleft Lip Cleft Lip/palate Clonorchiasis Coach Syndrome Cockayne Syndrome Cohen-Gibson Syndrome Colitis Colon Adenocarcinoma Combined Pituitary Hormone Deficiency Congenital Diarrhea Congenital Disorder of Glycosylation, Type Iic Congenital Hepatic Fibrosis Crigler-Najjar Syndrome, Type Ii Cystadenoma Cystic Fibrosis Cytochrome P450 2d6 Variant Cytomegalic Inclusion Disease Diabetes Insipidus Diabetes Mellitus Diarrhea Diarrhea 2, with Microvillus Atrophy Dilated Cardiomyopathy Down Syndrome Dubin-Johnson Syndrome Duodenal Gastrinoma Duodenal Obstruction Duodenitis Dwarfism Eclampsia Ehrlichiosis Endotheliitis Epithelial Recurrent Erosion Dystrophy Extrahepatic Cholestasis Fanconi Anemia, Complementation Group E Fascioliasis Galactosemia Gallbladder Cancer Gallbladder Disease Ganglioneuroma Gastrinoma Gastrointestinal Lymphoma Gastrointestinal Stromal Tumor Gastroschisis Gestational Diabetes Glycerol Kinase Deficiency Granulomatous Hepatitis Graves' Disease Hardikar Syndrome Hellp Syndrome Hemolytic Anemia Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatic Tuberculosis Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatopulmonary Syndrome Hereditary Lymphedema Hereditary Spherocytosis Histiocytosis Histoplasmosis Human Coronavirus Sensitivity Hydranencephaly Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperbilirubinemia, Rotor Type Hypercholesterolemia, Autosomal Dominant, 3 Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hypermethioninemia Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypervitaminosis a Hypoglycemia Hypogonadism Hypoxia Ichthyosis Idiopathic Ductopenia Immune Hydrops Fetalis Impetigo Impetigo Herpetiformis Inappropriate Adh Syndrome Insulin-Like Growth Factor I Intestinal Atresia Intestinal Perforation Intrahepatic Cholestasis Ischemia Isolated Growth Hormone Deficiency, Type Ia Kawasaki Disease Kwashiorkor Lactic Acidosis Langerhans Cell Histiocytosis Light Chain Deposition Disease Lipid Storage Disease Lipoid Congenital Adrenal Hyperplasia Liver Cirrhosis Liver Disease Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lupus Erythematosus Lymphedema Lymph Node Tuberculosis Lymphoma Malaria Mccune-Albright Syndrome Meconium Ileus Microcephaly, Epilepsy, and Diabetes Syndrome Microphthalmia Mirizzi Syndrome Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Myeloma, Multiple Myopathy Myopathy, Centronuclear, X-Linked Myotonic Dystrophy Neonatal Jaundice Neonatal Lupus Erythematosus Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronitis Niemann-Pick Disease Nodular Regenerative Hyperplasia Obstructive Jaundice Opisthorchiasis Orbital Cyst Ovarian Hyperstimulation Syndrome Pancreatic Cancer Pancreatic Cystadenoma Pancreatitis Pancytopenia Paraneoplastic Syndromes Paraquat Poisoning Peliosis Hepatis Pemphigoid Gestationis Pericardial Effusion Peritonitis Perlman Syndrome Persistent Idiopathic Facial Pain Peutz-Jeghers Syndrome Pheochromocytoma Pick Disease of Brain Pituitary Hormone Deficiency, Combined, 2 Pituitary Stalk Interruption Syndrome Plasmacytoma Plasmodium Vivax Malaria Pneumonia Polycystic Kidney Disease Polymorphic Reticulosis Porphyria Porphyria Cutanea Tarda Portal Hypertension Pre-Eclampsia Prieto X-Linked Mental Retardation Syndrome Primary Biliary Cirrhosis Protein-Losing Enteropathy Psoriasis Psoriasis 13 Pulmonic Stenosis Pure Red-Cell Aplasia Purpura Pustular Psoriasis Rapp-Hodgkin Syndrome Relapsing Polychondritis Renal Tubular Acidosis Retinitis Retinitis Pigmentosa Retroperitoneal Fibrosis Rickets Riddle Syndrome Sarcoidosis 2 Sclerosing Cholangitis Short Bowel Syndrome Sialadenitis Sickle Cell Anemia Sickle Cell Disease Siderosis Smith-Lemli-Opitz Syndrome Spinal and Bulbar Muscular Atrophy, X-Linked 1 Steatorrhea Systemic Mastocytosis Three M Syndrome 1 Thrombocytopenia Thyroiditis Typhoid Fever Tyrosinemia Ulcerative Colitis Uveitis Van Der Woude Syndrome 1 Ventricular Fibrillation, Paroxysmal Familial, 1 Viral Hepatitis Wilson Disease Xanthogranulomatous Cholecystitis Xanthomatosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome