13920009: Hepatic encephalopathy (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Metabolic encephalopathy\Hepatic encephalopathy
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Metabolic encephalopathy\Hepatic encephalopathy

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Metabolic encephalopathy\Hepatic encephalopathy
\Central nervous system finding\Disorder of the central nervous system (disorder)\Central nervous system complication\Hepatic encephalopathy
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Metabolic encephalopathy\Hepatic encephalopathy

\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Central nervous system complication\Hepatic encephalopathy
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Metabolic encephalopathy\Hepatic encephalopathy
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Metabolic encephalopathy\Hepatic encephalopathy
\Disease\Metabolic disease\Metabolic encephalopathy\Hepatic encephalopathy

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

23734015 Hepatic encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

23736018 Hepatocerebral encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

475600012 HE - Hepatic encephalopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

739420013 Hepatic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

930981000195110 encefalopatia epatica it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1901000172118 encéphalopathie hépatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2326831000195113 HE - hepatische Enzephalopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2326841000195117 Hepatische Enzephalopathie de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hepatic encephalopathy	Is a	Disease of liver	false	Inferred relationship	Some
Hepatic encephalopathy	Is a	encéphalopathies toxiques et métaboliques acquises	false	Inferred relationship	Some
Hepatic encephalopathy	Is a	Metabolic encephalopathy	true	Inferred relationship	Some
Hepatic encephalopathy	Finding site	Liver structure	false	Inferred relationship	Some
Hepatic encephalopathy	Finding site	Brain tissue structure	false	Inferred relationship	Some
Hepatic encephalopathy	Finding site	Brain structure	true	Inferred relationship	Some	1
Hepatic encephalopathy	Due to	Disease of liver	true	Inferred relationship	Some	2
Hepatic encephalopathy	Is a	Central nervous system complication	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hepatic coma	Is a	True	Hepatic encephalopathy	Inferred relationship	Some
Hepatic encephalopathy in fulminant hepatic failure	Is a	True	Hepatic encephalopathy	Inferred relationship	Some
Portal systemic encephalopathy	Is a	True	Hepatic encephalopathy	Inferred relationship	Some
A rare, inherited mitochondrial disorder due to a defect in mitochondrial protein synthesis characterized by intrauterine growth retardation, metabolic decompensation with recurrent vomiting, persistent severe lactic acidosis, encephalopathy, seizures, failure to thrive, severe global developmental delay, poor eye contact, severe muscular hypotonia or axial hypotonia with limb hypertonia, hepatomegaly and/or liver dysfunction and/or liver failure, leading to fatal outcome in severe cases. Neuroimaging abnormalities may include corpus callosum thinning, leukodystrophy, delayed myelination and basal ganglia involvement.	Is a	True	Hepatic encephalopathy	Inferred relationship	Some
Delirium due to hepatic encephalopathy	Due to	True	Hepatic encephalopathy	Inferred relationship	Some	2

Reference Sets