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 adenine phosphoribosyltransferase\Adenine phosphoribosyl transferase deficiency type II
• \Metabolic disease\Disorder of purine and pyrimidine metabolism\Disorder of purine metabolism\Deficiency of adenine phosphoribosyltransferase\Adenine phosphoribosyl transferase deficiency type II
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of adenine phosphoribosyltransferase\Adenine phosphoribosyl transferase deficiency type II

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356741016	Adenine phosphoribosyl transferase deficiency type II	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
626828016	Adenine phosphoribosyl transferase deficiency type II (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start