267454002: Acatalasemia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\White blood cell disorder\Non-malignant white cell disorder\Acatalasaemia
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Acatalasaemia
• \Disease\Disorder of immune function\White blood cell disorder\Non-malignant white cell disorder\Acatalasaemia
• \Disease\Blood disease\White blood cell disorder\Non-malignant white cell disorder\Acatalasaemia
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Acatalasaemia
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Acatalasaemia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3010281013	Takahara disease	en	Synonym	Active	Case sensitive	SNOMED CT core
3011706011	Acatalasia	en	Synonym	Active	Case insensitive	SNOMED CT core
398894016	Acatalasemia	en	Synonym	Active	Case insensitive	SNOMED CT core
398895015	Catalase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
398896019	Acatalasaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
660072011	Acatalasemia (disorder)	en	Fully specified name	Active	Case insensitive	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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