30102006: Glucose-6-phosphate transport defect (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Viscus structure finding (finding)\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Digestive system finding (finding)\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Digestive system finding (finding)\maladie de l'appareil digestif\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\trouble métabolique\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\trouble métabolique\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\trouble métabolique\Disorder of carbohydrate metabolism\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate transport defect
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form\Glycogen storage disease, type I\Glucose-6-phosphate 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
484483017	Glycogen storage disease type Ib	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
484484011	Glucose 6-phosphate transport defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
50375011	Glucose-6-phosphate transport defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
761070014	Glucose-6-phosphate transport defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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