124115002: Deficiency of L-lactate dehydrogenase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Lactate dehydrogenase deficiency\Deficiency of L-lactate dehydrogenase
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Lactate dehydrogenase deficiency\Deficiency of L-lactate dehydrogenase
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of L-lactate dehydrogenase
• \Metabolic disease\Disorder of carbohydrate metabolism\Lactate dehydrogenase deficiency\Deficiency of L-lactate dehydrogenase
• \Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Lactate dehydrogenase deficiency\Deficiency of L-lactate dehydrogenase

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
203514012	Deficiency of lactic acid dehydrogenase	en	Synonym	Active	Case insensitive	SNOMED CT core
203515013	Deficiency of L-lactate dehydrogenase	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
727600017	Deficiency of L-lactate dehydrogenase (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start