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\Purine and pyrimidine metabolism disorder\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, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1235531012	Orotidine-5-phosphate decarboxylase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
1235532017	Hereditary orotic aciduria type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
149333011	Hereditary orotic aciduria, type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
149334017	OMP decarboxylase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
149335016	Orotidine-5'-phosphate decarboxylase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
833125016	Hereditary orotic aciduria, type 2 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start