65791008: Adenine phosphoribosyltransferase deficiency, Japanese type (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Deficiency of adenine phosphoribosyltransferase\Adenine phosphoribosyltransferase deficiency, Japanese type
• \Metabolic disease\Disorder of purine and pyrimidine metabolism\Disorder of purine metabolism\Deficiency of adenine phosphoribosyltransferase\Adenine phosphoribosyltransferase deficiency, Japanese type
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of adenine phosphoribosyltransferase\Adenine phosphoribosyltransferase deficiency, Japanese type

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
109300016	APRT deficiency, Japanese type	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
2620973011	Adenine phosphoribosyltransferase (APRT) deficiency, Japanese type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2913515015	Adenine phosphoribosyltransferase deficiency, Japanese type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2914959012	Adenine phosphoribosyltransferase deficiency, Japanese type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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