237985009: Pearson's syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\Anaemia\Sideroblastic anaemia\Pearson's syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Pearson's syndrome
• \Disease\Blood disease\Anaemia\Sideroblastic anaemia\Pearson's syndrome
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Pearson's syndrome
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of pyruvate metabolism and mitochondrial respiratory chain\Pearson's syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2839083012	Pearson syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
356688011	Pearson's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
626799011	Pearson's 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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