Code System Concept

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Code System Concept

Code System Concept Code	50122000
Code System Concept Name	Metabolic encephalopathy (disorder)
Code System Preferred Concept Name	Metabolic encephalopathy (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Active
SDO Concept Status Date	01/31/2002
SDO Date Created	01/31/2002
SDO Date Revised	01/31/2002
Description
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
83497018	Metabolic encephalopathy	Active	Synonym	false	false
83498011	Metabolic brain syndrome	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	1
Disease	10 , 9 , 8 , 7 , 6 , 5 , 4 , 3 , 2 , 1
Problem Value Set	3 , 2 , 1

Parent Concepts

Parent Concepts

Parent/Child (Relationship Type)

Disorder of brain (disorder) {81308009 , SNOMED-CT } Metabolic disease (disorder) {75934005 , SNOMED-CT } Toxic metabolic encephalopathy (disorder) {472916000 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

Metabolic encephalopathy (disorder) {50122000 , SNOMED-CT }

Parent/Child (Relationship Type)

Anoxia of brain (disorder) {95645000 , SNOMED-CT } Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder) {773668008 , SNOMED-CT } Dialysis dementia (disorder) {9345005 , SNOMED-CT } Dialysis disequilibrium syndrome (disorder) {87235005 , SNOMED-CT } Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder) {1236807002 , SNOMED-CT } Encephalopathy due to vitamin deficiency (disorder) {230352008 , SNOMED-CT } Ethylmalonic encephalopathy (disorder) {811000124106 , SNOMED-CT } Glucose transporter protein type 1 deficiency syndrome (disorder) {445252005 , SNOMED-CT } Hepatic encephalopathy (disorder) {13920009 , SNOMED-CT } Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) {763721006 , SNOMED-CT } Hypertensive encephalopathy (disorder) {50490005 , SNOMED-CT } Hypoglycemic encephalopathy (disorder) {64624009 , SNOMED-CT } Hyponatremic encephalopathy (disorder) {230358007 , SNOMED-CT } Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency (disorder) {783734000 , SNOMED-CT } Myxedema coma (disorder) {21263006 , SNOMED-CT } Myxedema encephalopathy (disorder) {192816007 , SNOMED-CT } Progressive external ophthalmoplegia, myopathy, emaciation syndrome (disorder) {764733009 , SNOMED-CT } Progressive polyneuropathy with bilateral striatal necrosis (disorder) {771305006 , SNOMED-CT } Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) {1172698005 , SNOMED-CT } Secondary amyloid encephalopathy (disorder) {230359004 , SNOMED-CT } Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder) {771516000 , SNOMED-CT } Uremic encephalopathy (disorder) {35145002 , SNOMED-CT }

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,