Hepatic Encephalopathy

Alias:
Hepatic Encephalopathy, Stage Unspecified
Portal-Systemic Encephalopathy
He - [hepatic Encephalopathy]
Hepatocerebral Encephalopathy
Hepatocerebral Intoxication
Hepatic Encephalopathy Nos
Encephalopathy, Hepatic
Hepatic Coma
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hepatic Encephalopathy, also known as portal-systemic encephalopathy, is related to hepatic coma and hepatorenal syndrome. An important gene associated with Hepatic Encephalopathy is F2 (Coagulation Factor II, Thrombin), and among its related pathways/superpathways are Metabolism and Immune response IL-23 signaling pathway. The drugs Midazolam and Propofol have been mentioned in the context of this disorder. Affiliated tissues include liver and brain, and related phenotypes are homeostasis/metabolism and nervous system
Related ID:
MESH:D006501
ICD11:1769383160

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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32
382
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Medical Symptom

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Description
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No data available

Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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