29692004: Combined molybdoflavoprotein enzyme deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency
• \Metabolic disease\Hereditary metabolic disease\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency
• \Metabolic disease\Purine and pyrimidine metabolism disorder\Disorder of purine metabolism\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency
• \Metabolic disease\Enzymopathy\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
484364013	Hereditary xanthinuria type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
484365014	Molybdenum cofactor deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
484366010	Combined xanthine oxidase and aldehyde oxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
484367018	Xanthine oxidase-sulphite oxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
484368011	Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
484369015	Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
49668019	Combined molybdoflavoprotein enzyme deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
49669010	Hereditary xanthinuria, type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
49670011	Deficiency of molybdenum cofactor	en	Synonym	Active	Case insensitive	SNOMED CT core
49671010	Xanthine oxidase-sulfite oxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
760614019	Combined molybdoflavoprotein enzyme 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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