1003849000: Pyruvate dehydrogenase complex E2 subunit deficiency (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Inborn error of pyruvate metabolism (disorder)\Pyruvate dehydrogenase complex deficiency\Pyruvate dehydrogenase complex E2 subunit deficiency
• \trouble métabolique\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Inborn error of pyruvate metabolism (disorder)\Pyruvate dehydrogenase complex deficiency\Pyruvate dehydrogenase complex E2 subunit deficiency
• \trouble métabolique\Disorder of acid-base balance\acidose\acidose métabolique\Metabolic acidosis, increased anion gap (disorder)\Metabolic acidosis, increased anion gap, accumulation of organic acids (disorder)\Lactic acidosis\Pyruvate dehydrogenase complex deficiency\Pyruvate dehydrogenase complex E2 subunit deficiency
• \Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Inborn error of pyruvate metabolism (disorder)\Pyruvate dehydrogenase complex deficiency\Pyruvate dehydrogenase complex E2 subunit deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4166816017	Pyruvate dehydrogenase complex E2 subunit deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4166817014	Pyruvate dehydrogenase complex E2 subunit deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

US English

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