773549000: maternale riboflavinedeficiëntie (aandoening)

• 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\Undernutrition\Deficiency of micronutrients\Vitamin deficiency (disorder)\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency
• \Nutritional disorder\Vitamin disease (disorder)\Disorder of vitamin B (disorder)\Vitamin B deficiency\Ariboflavinosis\Maternal riboflavin deficiency
• \Nutritional disorder\Vitamin disease (disorder)\Vitamin deficiency (disorder)\Vitamin B deficiency\Ariboflavinosis\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
6363211000146117	maternale riboflavinedeficiëntie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6363221000146110	maternale lactoflavinedeficiëntie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6363231000146112	maternale riboflavinedeficiëntie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6363241000146116	vitamine B2-tekort bij moeder	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
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

Expanded Value Set

This concept is not in any reference sets

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