25792000: Kearns-Sayre syndrome (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\Kearns-Sayre syndrome
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Kearns-Sayre syndrome
• \Metabolic disease\Mitochondrial cytopathy\Kearns-Sayre syndrome
• \Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Kearns-Sayre syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1224922018	Kearns-Sayre mitochondrial cytopathy	en	Synonym	Active	Case sensitive	SNOMED CT core
1224923011	Mitochondrial ocular myopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
1224924017	KSS - Kearns-Sayre syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3755650016	Oculocraniosomatic syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
43223013	Kearns-Sayre syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
756150016	Kearns-Sayre syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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