773549000: Maternal riboflavin deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Maternal riboflavin deficiency
• \Nutritional disorder\Nutritional deficiency disorder\Undernutrition\Deficiency of micronutrients\Vitamin deficiency\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency
• \Nutritional disorder\Vitamin disease\Disorder of vitamin B\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency
• \Nutritional disorder\Vitamin disease\Vitamin deficiency\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3724047013	Maternal riboflavin deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3724048015	Maternal riboflavin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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