57863006: Acid phosphatase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Acid phosphatase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Acid phosphatase deficiency
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Acid phosphatase deficiency
• \Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Acid phosphatase deficiency
• \Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Acid phosphatase deficiency
• \Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Acid phosphatase deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
796532014	Acid phosphatase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
96212015	Acid phosphatase deficiency	en	Synonym	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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