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50122000: Metabolic encephalopathy (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Toxic metabolic encephalopathy\Metabolic encephalopathy
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Toxic metabolic encephalopathy\Metabolic encephalopathy

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Toxic metabolic encephalopathy\Metabolic encephalopathy

\Disorder of head\Disorder of brain\Toxic metabolic encephalopathy\Metabolic encephalopathy

\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Toxic metabolic encephalopathy\Metabolic encephalopathy
\Disease\Disorder of head\Disorder of brain\Toxic metabolic encephalopathy\Metabolic encephalopathy
\Disease\Metabolic disease\Metabolic encephalopathy

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

83497018 Metabolic encephalopathy en Synonym Active Entire term case insensitive SNOMED CT core module

83498011 Metabolic brain syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

787876019 Metabolic encephalopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Metabolic encephalopathy	Is a	Metabolic disease	true	Inferred relationship	Existential restriction modifier
Metabolic encephalopathy	Is a	Disorder of brain	false	Inferred relationship	Existential restriction modifier
Metabolic encephalopathy	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
Metabolic encephalopathy	Is a	Toxic metabolic encephalopathy	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hepatic encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Uremic encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Hypertensive encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Hypoglycemic encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Dialysis disequilibrium syndrome	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Dialysis dementia	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Anoxia of brain	Is a	False	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Glucose transporter protein type 1 deficiency syndrome	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Myxedema encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Myxedema coma	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Encephalopathy due to vitamin deficiency	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Hyponatremic encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Secondary amyloid encephalopathy	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Hypermethioninemia encephalopathy due to deficiency of adenosine kinase	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Progressive external ophthalmoplegia, myopathy, emaciation syndrome	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Progressive polyneuropathy with bilateral striatal necrosis	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Solute carrier family 35 member A2 congenital disorder of glycosylation	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Encephalopathy due to mitochondrial and peroxisomal fission defect	Is a	True	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier
Glucose transporter protein type 1 deficiency syndrome	Is a	False	Metabolic encephalopathy	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
83497018	Metabolic encephalopathy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
83498011	Metabolic brain syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
787876019	Metabolic encephalopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module