OMOP Concept 372892
Metabolic encephalopathy
StandardConditionSNOMED50122000Disorder
Maps from
7
Descendants
47
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Metabolic encephalopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134267 | Metabolic encephalopathy | Non-standard |
| ICD10CM | G93.41 | Metabolic encephalopathy | Non-standard |
| ICD10GM | G94.30 | Encephalopathy in endocrine and metabolic disorders classified elsewhere (machine translation) | Non-standard |
| ICD9CM | 348.31 | Metabolic encephalopathy | Non-standard |
| KCD7 | G93.80 | Metabolic encephalopathy | Non-standard |
| MeSH | D001928 | Brain Diseases, Metabolic | Non-standard |
| Nebraska Lexicon | 50122000 | Metabolic brain syndrome | Non-standard |
Synonyms
Alternative names recorded for Metabolic encephalopathy across source vocabularies.
- Metabolic brain syndrome
- Metabolic encephalopathy (disorder)
- síndrome cerebral metabólico
- síndrome cerebral metabólico (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
Narrower concepts
(47)Included automatically when you query with descendants.
- 1Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
- 1Dialysis dementia
- 1Dialysis disequilibrium syndrome
- 1Encephalopathy due to mitochondrial and peroxisomal fission defect
- 1Encephalopathy due to vitamin deficiency
- 1Glucose transporter protein type 1 deficiency syndrome
- 1Hepatic encephalopathy
- 1Hypermethioninemia encephalopathy due to deficiency of adenosine kinase
- 1Hypertensive encephalopathy
- 1Hypoglycemic encephalopathy
- 1Hyponatremic encephalopathy
- 1Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- 1Myxedema coma
- 1Myxedema encephalopathy
- 1Progressive external ophthalmoplegia, myopathy, emaciation syndrome
- 1Progressive polyneuropathy with bilateral striatal necrosis
- 1Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome
- 1Secondary amyloid encephalopathy
- 1Solute carrier family 35 member A2 congenital disorder of glycosylation
- 1Uremic encephalopathy
- 2Acute hepatic encephalopathy
- 2Cerebral degeneration due to beriberi
- 2Cerebral degeneration due to vitamin B12 deficiency
- 2Hepatic coma
- 2Hepatic encephalopathy in fulminant hepatic failure
- 2Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- 2Iatrogenic myxedema coma
- 2Myxedema coma due to subclinical hypothyroidism
- 2Portal systemic encephalopathy
- 2Uremic coma
- 3Hepatic coma due to acute hepatic failure
- 3Hepatic coma due to alcoholic liver failure
- 3Hepatic coma due to chronic hepatic failure
- 3Hepatic coma due to hepatitis
- 3Hepatic coma due to subacute liver failure
- 4Hepatic coma due to viral hepatitis
- 5Hepatic coma due to viral hepatitis A
- 5Hepatic coma due to viral hepatitis B
- 5Hepatic coma due to viral hepatitis C
- 5Hepatic coma due to viral hepatitis D
- 6Chronic viral hepatitis C with hepatic coma
- 6Hepatic coma due to acute hepatitis B
- 6Hepatic coma due to acute hepatitis B with delta agent
- 6Hepatic coma due to acute hepatitis C
- 6Hepatic coma due to chronic hepatitis B
- 6Hepatic coma due to chronic hepatitis B with delta agent
- 6Hepatic coma due to chronic hepatitis C
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