297255007: Hepatic glycogen phosphorylase kinase deficiency (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
437744011	Hepatic glycogen phosphorylase kinase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
692567011	Hepatic glycogen phosphorylase kinase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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