20307000: Ariboflavinosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Nutritional disorder\...

\Nutritional deficiency disorder\Undernutrition\Deficiency of micronutrients\Vitamin deficiency\Vitamin B deficiency\Ariboflavinosis

\Vitamin disease\Disorder of vitamin B (disorder)\Vitamin B deficiency\Ariboflavinosis
\Vitamin disease\Vitamin deficiency\Vitamin B deficiency\Ariboflavinosis

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

34149017 Ariboflavinosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

34150017 Vitamin B2 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

34151018 Riboflavin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

749367013 Ariboflavinosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1222421016 Riboflavine deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1989781000005118 ariboflavinose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Ariboflavinosis	Is a	Vitamin deficiency	false	Inferred relationship	Some
Ariboflavinosis	Finding site	Body system structure	false	Inferred relationship	Some
Ariboflavinosis	Is a	Vitamin B deficiency	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Gopalan's syndrome	Is a	True	Ariboflavinosis	Inferred relationship	Some
Anemia due to riboflavin deficiency	Associated etiologic finding	False	Ariboflavinosis	Inferred relationship	Some
Anemia due to riboflavin deficiency	Due to	True	Ariboflavinosis	Inferred relationship	Some	3
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.	Is a	True	Ariboflavinosis	Inferred relationship	Some

This concept is not in any reference sets