297252005: Glycogen phosphorylase kinase deficiency, autosomal recessive (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

\Digestive system finding\Liver finding\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive
\Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive

\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
\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
\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
\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

\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
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive
\Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive
\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
\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
\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
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen phosphorylase kinase deficiency\Glycogen phosphorylase kinase deficiency, autosomal recessive

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

Descriptions:

Id Description Lang Type Status Case? Module

437741015 Glycogen phosphorylase kinase deficiency, autosomal recessive en Synonym Active Case insensitive SNOMED CT core

692563010 Glycogen phosphorylase kinase deficiency, autosomal recessive (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cardiac glycogen phosphorylase kinase deficiency	Is a	True	Glycogen phosphorylase kinase deficiency, autosomal recessive	Inferred relationship	Some
Hepatic and muscle glycogen phosphorylase kinase deficiency	Is a	True	Glycogen phosphorylase kinase deficiency, autosomal recessive	Inferred relationship	Some
Hepatic glycogen phosphorylase kinase deficiency	Is a	True	Glycogen phosphorylase kinase deficiency, autosomal recessive	Inferred relationship	Some

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
437741015	Glycogen phosphorylase kinase deficiency, autosomal recessive	en	Synonym	Active	Case insensitive	SNOMED CT core
692563010	Glycogen phosphorylase kinase deficiency, autosomal recessive (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core