238010006: Adenine phosphoribosyl transferase deficiency type II (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 II
• \Metabolic disease\Purine and pyrimidine metabolism disorder\Disorder of purine metabolism\Deficiency of AMP pyrophorylase\Adenine phosphoribosyl transferase deficiency type II
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of AMP pyrophorylase\Adenine phosphoribosyl transferase deficiency type II

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356741016	Adenine phosphoribosyl transferase deficiency type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
626828016	Adenine phosphoribosyl transferase deficiency type II (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

Problem/Diagnosis reference set

Back to Start