7265005: Glycogen storage disease, type I (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I

\Digestive system finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Glycogen storage disease, type I
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen storage disease, hepatic form\Glycogen storage disease, type I
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, hepatic form\Glycogen storage disease, type I

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease, type I	Is a	Glycogen storage disease	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Congenital anomaly of liver	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Finding site	Digestive organ structure	false	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Finding site	Liver structure	false	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Is a	Congenital anomaly of skeletal muscle	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Finding site	Structure of digestive system	false	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Glycogen storage disease, hepatic form	true	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Congenital anomaly of digestive organ	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Congenital anomaly of abdomen	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Congenital anomaly of body cavity	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Is a	Lesion of liver	false	Inferred relationship	Existential restriction modifier
Glycogen storage disease, type I	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease, type I	Finding site	Liver structure	true	Inferred relationship	Existential restriction modifier	2
Glycogen storage disease, type I	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glycogen storage disease type Ia	Is a	True	Glycogen storage disease, type I	Inferred relationship	Existential restriction modifier
Glucose-6-phosphate transport defect	Is a	True	Glycogen storage disease, type I	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
12994015	Glycogen storage disease, type I	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
12995019	Hepatorenal glycogen storage disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
12997010	von Gierke's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
12998017	GSD I	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
502178014	Liver glycogen disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
502179018	von Gierke disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
812951015	Glycogen storage disease, type I (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3037037019	Glycogen storage disease, type 1	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module