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

Expanded Value Set

This concept is not in any reference sets

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