OMOP Concept 43021132
Toxic metabolic encephalopathy
StandardConditionSNOMED472916000Disorder
Maps from
4
Descendants
72
Valid from
31 Jan 2013
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Toxic metabolic encephalopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10GM | G94.31 | Encephalopathy in infectious and parasitic diseases classified elsewhere (machine translation) | Non-standard |
| ICD9CM | 323.7 | Toxic encephalitis, myelitis, and encephalomyelitis | Non-standard |
| ICD9CM | 323.71 | Toxic encephalitis and encephalomyelitis | Non-standard |
| Nebraska Lexicon | 472916000 | Toxic and/or metabolic encephalopathy | Non-standard |
Synonyms
Alternative names recorded for Toxic metabolic encephalopathy across source vocabularies.
- encefalopatía metabólica tóxica
- encefalopatía metabólica tóxica (trastorno)
- Toxic and/or metabolic encephalopathy
- Toxic metabolic encephalopathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(72)Included automatically when you query with descendants.
- 1Alcoholic encephalopathy
- 1Encephalopathy caused by ionizing radiation
- 1Encephalopathy with sepsis
- 1Metabolic encephalopathy
- 1Reye's syndrome
- 1Toxic encephalitis
- 1Toxic encephalopathy
- 1Urate encephalopathy
- 2Ammonia encephalopathy
- 2Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
- 2Dialysis dementia
- 2Dialysis disequilibrium syndrome
- 2Drug-induced encephalopathy
- 2Encephalopathy caused by heavy metal
- 2Encephalopathy due to mitochondrial and peroxisomal fission defect
- 2Encephalopathy due to vitamin deficiency
- 2Encephalopathy following radiation therapy
- 2Glucose transporter protein type 1 deficiency syndrome
- 2Hepatic encephalopathy
- 2Hyperammonemic encephalopathy
- 2Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
- 2Hypertensive encephalopathy
- 2Hypoglycemic encephalopathy
- 2Hyponatremic encephalopathy
- 2Korsakoff's psychosis
- 2Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- 2Morel laminar sclerosis
- 2Myxedema coma
- 2Myxedema encephalopathy
- 2Progressive external ophthalmoplegia, myopathy, emaciation syndrome
- 2Progressive polyneuropathy with bilateral striatal necrosis
- 2Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome
- 2Secondary amyloid encephalopathy
- 2Solute carrier family 35 member A2 congenital disorder of glycosylation
- 2Toxic encephalitis caused by thallium
- 2Toxic encephalomyelitis
- 2Toxic encephalopathy caused by carbon tetrachloride
- 2Toxic encephalopathy caused by hydroxyquinoline
- 2Toxic encephalopathy caused by monomethyl mercury
- 2Uremic encephalopathy
- 3Acute hepatic encephalopathy
- 3Cerebral degeneration due to beriberi
- 3Cerebral degeneration due to vitamin B12 deficiency
- 3Hepatic coma
- 3Hepatic encephalopathy in fulminant hepatic failure
- 3Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- 3Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
- 3Iatrogenic myxedema coma
- 3Korsakov's alcoholic psychosis with peripheral neuritis
- 3Myxedema coma due to subclinical hypothyroidism
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