398664009: Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Deficiency of transferase\Deficiency of UTP-hexose-1-phosphate uridylyltransferase

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1778188017	Deficiency of UTP-hexose-1-phosphate uridylyltransferase	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
1786514018	UTP-hexose-1-phosphate uridyltransferase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
2914538014	Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase	en	Synonym	Active	Case insensitive	SNOMED CT core
2914763012	Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase (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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