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:
expandBrain Diseases, Metabolic (D001928)
Parent Node:
expandLiver Failure (D017093)
..Starting node
..expandHepatic Encephalopathy (D006501)

       Child Nodes:
........expandCombined Oxidative Phosphorylation Deficiency 1 (C563797)
........expandMITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) (OMIM:251880)



 Sister Nodes: 
..expandEnd Stage Liver Disease (D058625)
..expandHepatic Encephalopathy (D006501) Child2
..expandLiver Failure, Acute (D017114) Child3
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5074
Name:Hepatic Encephalopathy
Definition:A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5)
Alternative IDs:
ParentIDs:MESH:D001928|MESH:D017093
TreeNumbers:C06.552.308.500.356 |C10.228.140.163.360 |C18.452.132.360
Synonyms:Coma, Hepatic |Comas, Hepatic |Encephalopathies, Hepatic |Encephalopathies, Hepatocerebral |Encephalopathies, Portal-Systemic |Encephalopathies, Portosystemic |Encephalopathy, Hepatic |Encephalopathy, Hepatocerebral |Encephalopathy, Portal Systemic |Encephalopath
Slim Mappings:Digestive system disease|Metabolic disease|Nervous system disease
Reference: MedGen: D006501
MeSH: D006501
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants