237966006: Glucose transport defect (disorder)

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

\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glucose transport defect

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glucose transport defect

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glucose transport defect
\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glucose transport defect

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

356655016 Glucose transport defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

356656015 Glycogen storage disease type Id en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

626777015 Glucose transport defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glucose transport defect	Is a	Glycogen storage disease	true	Inferred relationship	Some
Glucose transport defect	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Glucose transport defect	Finding site	Liver structure	false	Inferred relationship	Some
Glucose transport defect	Occurrence	Congenital	true	Inferred relationship	Some	1
Glucose transport defect	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets