234407001: Uridine monophosphate hydrolase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\Red blood cell disorder\Erythrocyte enzyme deficiency\Uridine monophosphate hydrolase deficiency
• \Disease\Blood disease\Red blood cell disorder\Erythrocyte enzyme deficiency\Uridine monophosphate hydrolase deficiency
• \Disease\Disorder of body system\Red blood cell disorder\Erythrocyte enzyme deficiency\Uridine monophosphate hydrolase deficiency
• \Disease\Metabolic disease\Purine and pyrimidine metabolism disorder\Uridine monophosphate hydrolase deficiency

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351202015	Uridine monophosphate hydrolase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
351203013	Pyrimidine-5-nucleotidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
622721019	Uridine monophosphate hydrolase deficiency (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

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