297252005: Glycogen phosphorylase kinase deficiency, autosomal recessive (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\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Digestive system finding (finding)\constatation à propos du foie\affection du foie\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Digestive system finding (finding)\maladie de l'appareil digestif\Digestive system hereditary disorder\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \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\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \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\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\affection du foie\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\trouble métabolique\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\trouble métabolique\Disorder of carbohydrate metabolism\maladie de stockage du glycogène (trouble)\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease type IX (disorder)\Glycogen phosphorylase kinase deficiency, autosomal recessive

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
437741015	Glycogen phosphorylase kinase deficiency, autosomal recessive	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
692563010	Glycogen phosphorylase kinase deficiency, autosomal recessive (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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