773549000: Maternal riboflavin deficiency (disorder)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3724047013	Maternal riboflavin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3724048015	Maternal riboflavin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
3724047013	Maternal riboflavin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3724048015	Maternal riboflavin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
3422821001000119	Riboflavin-Mangel, maternaler	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
884611000172113	déficit maternel en riboflavine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
884611000172113	déficit maternel en riboflavine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3422821001000119	Riboflavin-Mangel, maternaler	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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