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

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
356740015	Adenine phosphoribosyl transferase deficiency type I	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
626827014	Adenine phosphoribosyl transferase deficiency type I (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