Disease Browser
Parent Node: Liver Diseases (D008107) ..Starting node .. Hepatic Insufficiency (D048550) Child Nodes:
........Liver Failure (D017093) 8 Sister Nodes: ..alpha 1-Antitrypsin Deficiency (D019896) 1 ..Budd-Chiari Syndrome (D006502) 1 ..Carnitine Palmitoyltransferase II Deficiency, Infantile (C563462) ..Cholestasis, Intrahepatic (D002780) 14 ..COACH syndrome (C536430) ..Congenital Hepatic Fibrosis (C580013) ..Cyanosis and Hepatic Disease (C565660) ..Drug-Induced Liver Injury (D056486) 2 ..Fatty Liver (D005234) 6 ..Focal Nodular Hyperplasia (D020518) ..Glycogen Storage Disease 0, Liver (C565485) ..GSD IV, Nonprogressive Hepatic (C565540) ..Hepatic Insufficiency (D048550) 9 ..Hepatic Veno-Occlusive Disease (D006504) 1 ..Hepatitis (D006505) 17 ..Hepatolenticular Degeneration (D006527) 2 ..Hepatomegaly (D006529) 4 ..Hepatopulmonary Syndrome (D020065) ..Hepatorenal Syndrome (D006530) ..Hypertension, Portal (D006975) 3 ..Liver Abscess (D008100) 2 ..Liver Cirrhosis (D008103) 16 ..Liver Diseases, Alcoholic (D008108) 3 ..Liver Diseases, Parasitic (D008109) 5 ..Liver Fibrocystic Disease and Polydactyly (C565272) ..Liver Neoplasms (D008113) 8 ..Navajo neurohepatopathy (C538344) 1 ..Peliosis Hepatis (D010382) ..Phosphoenolpyruvate carboxykinase deficiency (C536654) ..Polycystic liver disease (C536330) ..Porphyrias, Hepatic (D017094) 14 ..RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540) ..Retinohepatoendocrinologic Syndrome (C564839) ..Tuberculosis, Hepatic (D014386) ..Zellweger Syndrome (D015211) 3 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD