781386002: Deficiency of nudix hydrolase 15 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Genetic finding\Deficiency of nudix hydrolase 15
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Deficiency of nudix hydrolase 15
• \Disease\Metabolic disease\Disorder of purine and pyrimidine metabolism\Disorder of purine metabolism\Deficiency of nudix hydrolase 15

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3746928018	Deficiency of nudix hydrolase 15	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3746929014	Thiopurine poor metaboliser 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3746930016	NUDT15 deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3746931017	Thiopurine poor metabolizer 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3746932012	Deficiency of nudix hydrolase 15 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3746933019	Nucleotide diphosphatase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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