6075009: Glycogen storage disease, hepatic form (disorder)

SNOMED CT Concept\Clinical finding\...

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

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

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

11092017 Glycogen storage disease, hepatic form en Synonym Active Case insensitive SNOMED CT core

799737017 Glycogen storage disease, hepatic form (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease, hepatic form	Is a	Congenital anomaly of skeletal muscle	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	Finding site	Structure of digestive system	false	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
Glycogen storage disease, hepatic form	Is a	Congenital anomaly of trunk	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	Is a	Digestive system hereditary disorder	true	Inferred relationship	Some
Glycogen storage disease, hepatic form	Is a	Metabolic and genetic disorder affecting the liver	true	Inferred relationship	Some
Glycogen storage disease, hepatic form	Is a	Glycogen storage disease	true	Inferred relationship	Some
Glycogen storage disease, hepatic form	Is a	Congenital anomaly of liver	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	Occurrence	Congenital	true	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	Finding site	Digestive organ structure	false	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	Finding site	Liver structure	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glycogen storage disease, type VI	Is a	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease, type IV	Is a	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease type X	Is a	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease, type IX	Is a	False	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease type VIII	Is a	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease type III	Is a	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease, type I	Is a	True	Glycogen storage disease, hepatic form	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
11092017	Glycogen storage disease, hepatic form	en	Synonym	Active	Case insensitive	SNOMED CT core
799737017	Glycogen storage disease, hepatic form (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core