1003367004: Molybdenum cofactor deficiency complementation group A (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary metabolic disease\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group A
• \Metabolic disease\Hereditary metabolic disease\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group A
• \Metabolic disease\Disorder of purine and pyrimidine metabolism\Disorder of purine metabolism\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group A
• \Metabolic disease\Enzymopathy\Hereditary xanthinuria\Combined molybdoflavoprotein enzyme deficiency\Molybdenum cofactor deficiency complementation group A

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4168091018	Molybdenum cofactor deficiency complementation group A	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4168092013	Molybdenum cofactor deficiency complementation group A (disorder)	en	Fully specified name	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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