297255007: Hepatic glycogen phosphorylase kinase deficiency (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency

\Digestive system finding\Liver finding\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Glycogen phosphorylase kinase deficiency\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\Liver disease\Glycogen phosphorylase kinase deficiency\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\Liver disease\Glycogen phosphorylase kinase deficiency\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\Liver disease\Glycogen phosphorylase kinase deficiency\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\Liver disease\Glycogen phosphorylase kinase deficiency\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 phosphorylase kinase deficiency\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 phosphorylase kinase deficiency\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 phosphorylase kinase deficiency\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 phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency
\Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Liver disease\Glycogen phosphorylase kinase deficiency\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 phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive\Hepatic glycogen phosphorylase kinase deficiency

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

Descriptions:

Id Description Lang Type Status Case? Module

437744011 Hepatic glycogen phosphorylase kinase deficiency en Synonym Active Case insensitive SNOMED CT core

692567011 Hepatic glycogen phosphorylase kinase deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hepatic glycogen phosphorylase kinase deficiency	Is a	Glycogen phosphorylase kinase deficiency, autosomal recessive	true	Inferred relationship	Some
Hepatic glycogen phosphorylase kinase deficiency	Finding site	Body system structure	false	Inferred relationship	Some
Hepatic glycogen phosphorylase kinase deficiency	Occurrence	Congenital	false	Inferred relationship	Some
Hepatic glycogen phosphorylase kinase deficiency	Finding site	Liver structure	false	Inferred relationship	Some
Hepatic glycogen phosphorylase kinase deficiency	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Hepatic glycogen phosphorylase kinase deficiency	Occurrence	Congenital	true	Inferred relationship	Some	1
Hepatic glycogen phosphorylase kinase deficiency	Finding site	Liver structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

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