238009001: Adenine phosphoribosyl transferase deficiency type I (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Deficiency of AMP pyrophorylase\Adenine phosphoribosyl transferase deficiency type I
• \Metabolic disease\Purine and pyrimidine metabolism disorder\Disorder of purine metabolism\Deficiency of AMP pyrophorylase\Adenine phosphoribosyl transferase deficiency type I
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of AMP pyrophorylase\Adenine phosphoribosyl transferase deficiency type I

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356740015	Adenine phosphoribosyl transferase deficiency type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
626827014	Adenine phosphoribosyl transferase deficiency type I (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

Australian dialect reference set

Problem/Diagnosis reference set

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