235908005: Glycogen storage disease type IX (disorder)

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

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3441358013	Glycogen storage disease type IX (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
353637017	Glycogen phosphorylase kinase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
353639019	PHK - Hepatic phosphorylase kinase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
353640017	Hepatic phosphorylase kinase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
353641018	Phosphorylase kinase deficiency of liver	en	Synonym	Active	Case insensitive	SNOMED CT core
353642013	Glycogen storage disease type IX	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
353643015	Glycogenosis viiia	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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