860860004: Glycogen storage disease type IXB (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Digestive system finding\Liver finding\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen storage disease type IXB

Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3944369015	Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3977970010	Glycogen storage disease type IXB (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3977971014	Glycogen storage disease type IXB	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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