Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Digestive System Diseases (D004066)
..Starting node
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Liver Diseases (D008107)

       Child Nodes:
........expandalpha 1-Antitrypsin Deficiency (D019896) Child1
........expandBudd-Chiari Syndrome (D006502) Child1
........expandCarnitine Palmitoyltransferase II Deficiency, Infantile (C563462)
........expandCholestasis, Intrahepatic (D002780) Child14
........expandCOACH syndrome (C536430)
........expandCongenital Hepatic Fibrosis (C580013)
........expandCyanosis and Hepatic Disease (C565660)
........expandDrug-Induced Liver Injury (D056486) Child2
........expandFatty Liver (D005234) Child6
........expandFocal Nodular Hyperplasia (D020518)
........expandGlycogen Storage Disease 0, Liver (C565485)
........expandGSD IV, Nonprogressive Hepatic (C565540)
........expandHepatic Insufficiency (D048550) Child9
........expandHepatic Veno-Occlusive Disease (D006504) Child1
........expandHepatitis (D006505) Child17
........expandHepatolenticular Degeneration (D006527) Child2
........expandHepatomegaly (D006529) Child4
........expandHepatopulmonary Syndrome (D020065)
........expandHepatorenal Syndrome (D006530)
........expandHypertension, Portal (D006975) Child3
........expandLiver Abscess (D008100) Child2
........expandLiver Cirrhosis (D008103) Child16
........expandLiver Diseases, Alcoholic (D008108) Child3
........expandLiver Diseases, Parasitic (D008109) Child5
........expandLiver Fibrocystic Disease and Polydactyly (C565272)
........expandLiver Neoplasms (D008113) Child8
........expandNavajo neurohepatopathy (C538344) Child1
........expandPeliosis Hepatis (D010382)
........expandPhosphoenolpyruvate carboxykinase deficiency (C536654)
........expandPolycystic liver disease (C536330)
........expandPorphyrias, Hepatic (D017094) Child14
........expandRENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
........expandRetinohepatoendocrinologic Syndrome (C564839)
........expandTuberculosis, Hepatic (D014386)
........expandZellweger Syndrome (D015211) Child3



 Sister Nodes: 
..expandBiliary Tract Diseases (D001660) Child68
..expandDigestive System Abnormalities (D004065) Child78
..expandDigestive System Fistula (D016154) Child12
..expandDigestive System Neoplasms (D004067) Child99
..expandGastrointestinal Diseases (D005767) Child357
..expandLiver Diseases (D008107) Child135
..expandNovak syndrome (C537851)
..expandPancreatic Diseases (D010182) Child51
..expandPeritoneal Diseases (D010532) Child16
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6504
Name:Liver Diseases
Definition:Pathological processes of the LIVER.
Alternative IDs:
ParentIDs:MESH:D004066
TreeNumbers:C06.552
Synonyms:Disease, Liver |Diseases, Liver |Dysfunction, Liver |Dysfunctions, Liver |Liver Disease |Liver Dysfunction |Liver Dysfunctions
Slim Mappings:Digestive system disease
Reference: MedGen: D008107
MeSH: D008107
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants