6075009: Glycogen storage disease, hepatic form (disorder)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form

\Digestive system finding (finding)\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\Digestive system finding (finding)\maladie de l'appareil digestif\Digestive system hereditary disorder\Glycogen storage disease, hepatic form
\Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form

\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\constatation à propos d'un organe abdominal\constatation à propos du foie\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\constatation à propos d'une structure du tronc\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form
\Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form
\Disease\affection d'un système corporel\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen storage disease, hepatic form
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Digestive system hereditary disorder\Glycogen storage disease, hepatic form
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\Disease\affection du tronc\Disorder of abdominopelvic segment of trunk\affection abdominale\affection du foie\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\Disease\trouble métabolique\troubles métaboliques et génétiques affectant le foie\Glycogen storage disease, hepatic form
\Disease\trouble métabolique\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form
\Disease\trouble métabolique\Disorder of carbohydrate metabolism\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\maladie de stockage du glycogène (trouble)\Glycogen storage disease, hepatic form

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

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

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	est un(e) (attribut)	Congenital anomaly of skeletal muscle	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	localisation d'une constatation (attribut)	système digestif	false	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	2
Glycogen storage disease, hepatic form	est un(e) (attribut)	Congenital anomaly of trunk	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	est un(e) (attribut)	Digestive system hereditary disorder	true	Inferred relationship	Some
Glycogen storage disease, hepatic form	est un(e) (attribut)	troubles métaboliques et génétiques affectant le foie	true	Inferred relationship	Some
Glycogen storage disease, hepatic form	est un(e) (attribut)	maladie de stockage du glycogène (trouble)	true	Inferred relationship	Some
Glycogen storage disease, hepatic form	est un(e) (attribut)	Congenital anomaly of liver	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	localisation d'une constatation (attribut)	organe digestif (structure corporelle)	false	Inferred relationship	Some	1
Glycogen storage disease, hepatic form	localisation d'une constatation (attribut)	structure de muscle squelettique	false	Inferred relationship	Some
Glycogen storage disease, hepatic form	localisation d'une constatation (attribut)	foie	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glycogen storage disease, type VI	est un(e) (attribut)	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease, type IV	est un(e) (attribut)	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease type X	est un(e) (attribut)	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease, type IX	est un(e) (attribut)	False	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease type VIII	est un(e) (attribut)	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease type III	est un(e) (attribut)	True	Glycogen storage disease, hepatic form	Inferred relationship	Some
Glycogen storage disease, type I	est un(e) (attribut)	True	Glycogen storage disease, hepatic form	Inferred relationship	Some

Reference Sets

Canada French language reference set (foundation metadata concept)

Back to Start

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
799737017	Glycogen storage disease, hepatic form (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core