6075009: Glycogen storage disease, hepatic form (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form

\Finding of trunk structure\Liver finding\Disease of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form
\Finding of trunk structure\Disorder of trunk (disorder)\Disease of liver\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, hepatic form
\Disease\Fetal and/or neonatal disorder\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease, hepatic form
\Disease\Disorder of body system\Disease of liver\Metabolic and genetic disorder affecting the liver\Glycogen storage disease, hepatic form
\Disease\Disorder of trunk (disorder)\Disease of liver\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, 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, hepatic form

Status: current. Date: 31-Jan 2002

Descriptions:

Id Description Lang Type Status Case? Module

11092017 Glycogen storage disease, hepatic form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
11093010 Glycogen storage disease, hepatic form, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
799737017 Glycogen storage disease, hepatic form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease, hepatic form	Is a	Disorder of carbohydrate metabolism	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease, hepatic form	Is a	Metabolic and genetic disorder affecting the liver	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease, hepatic form	Is a	Storage disease	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease, hepatic form	Occurrence	Congenital	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	1
Glycogen storage disease, hepatic form	Finding site	Liver structure	true	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glycogen storage disease, type I	Is a	True	Glycogen storage disease, hepatic form	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease type III	Is a	True	Glycogen storage disease, hepatic form	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease, type VI	Is a	True	Glycogen storage disease, hepatic form	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease, type IV	Is a	True	Glycogen storage disease, hepatic form	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly
Glycogen storage disease type VIII	Is a	True	Glycogen storage disease, hepatic form	Congenital syphilitic hepatomegaly	Congenital syphilitic hepatomegaly

Reference Sets