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
• \Malnutrition\Nutritional deficiency disorder\Undernutrition\Deficiency of micronutrients\Vitamin deficiency\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency
• \Malnutrition\Vitamin disease\Disorder of vitamin B\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency
• \Malnutrition\Vitamin disease\Vitamin deficiency\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3724047013	Maternal riboflavin deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3724048015	Maternal riboflavin deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3724049011	A rare genetic disorder of metabolite absorption or transport with characteristics of persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical findings consistent with a secondary, life-threatening, transient multiple acyl-CoA dehydrogenase deficiency (MADD) in the newborn. The mother usually presents hyperemesis gravidarum in the absence of other features of riboflavin deficiency, such as skin lesions, jaundice, pruritus, sore mucous membranes, visual disturbances.	en	Definition	Active	Case sensitive	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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