90093009: Hereditary orotic aciduria, type 2 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Orotic aciduria\Hereditary orotic aciduria\Hereditary orotic aciduria, type 2
• \Metabolic disease\Disorder of purine and pyrimidine metabolism\Hereditary orotic aciduria, type 2
• \Metabolic disease\Disorder of pyrimidine metabolism\Orotic aciduria\Hereditary orotic aciduria\Hereditary orotic aciduria, type 2
• \Metabolic disease\Enzymopathy\Hereditary orotic aciduria\Hereditary orotic aciduria, type 2

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
149333011	Hereditary orotic aciduria, type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
149334017	OMP decarboxylase deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
149335016	Orotidine-5'-phosphate decarboxylase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
833125016	Hereditary orotic aciduria, type 2 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1235531012	Orotidine-5-phosphate decarboxylase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1235532017	Hereditary orotic aciduria type II	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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