297238008: Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Galactose epimerase deficiency\Erythrocyte uridine diphosphate galactose-4-epimerase deficiency
• \Metabolic disease\Enzymopathy\Specific enzyme deficiency\Galactose epimerase deficiency\Erythrocyte uridine diphosphate galactose-4-epimerase deficiency
• \Metabolic disease\Disorder of carbohydrate metabolism\Disorder of galactose metabolism\Galactosaemia\Galactose epimerase deficiency\Erythrocyte uridine diphosphate galactose-4-epimerase deficiency

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
437723011	Erythrocyte uridine diphosphate galactose-4-epimerase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
692548012	Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
988871000052112	brist på erytrocytär uridindifosfatgalaktos-4-epimeras	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

Back to Start