OMOP Concept 37163406
Ketoacidosis due to monocarboxylate transporter-1 deficiency
StandardConditionSNOMED1216941002Disorder
Maps from
0
Descendants
0
Valid from
30 Apr 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Ketoacidosis due to monocarboxylate transporter-1 deficiency across source vocabularies.
- cetoacidosis debida a deficiencia de transportador de monocarboxilato 1
- cetoacidosis debida a deficiencia de transportador de monocarboxilato 1 (trastorno)
- Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Inborn error of metabolism
- 1Ketoacidosis
- 1Metabolic disorder of transport
- 2Congenital disease
- 2Hereditary disease
- 2Hereditary metabolic disease
- 2Metabolic acidosis, IAG, accumulation of organic acids
- 2Metabolic disease
- 3Disease
- 3Fetal and/or neonatal disorder
- 3Genetic disease
- 3Metabolic acidosis, increased anion gap (IAG)
- 4Clinical finding
- 4Increased anion gap
- 4Metabolic acidosis
- 5Acidosis
- 5Disorder of electrolytes
- 6Disorder of acid-base balance
- 6Disorder of fluid AND/OR electrolyte
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