55912009: Glycogen storage disease, type V (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Musculoskeletal finding\Musculoskeletal disorder\...
• \Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Myopathy\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease, type V
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease, type V

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3035750013	Glycogen storage disease type 5	en	Synonym	Active	Case insensitive	SNOMED CT core
497455012	Glycogenosis, type 5	en	Synonym	Active	Case insensitive	SNOMED CT core
497456013	McArdle disease	en	Synonym	Active	Case sensitive	SNOMED CT core
497457016	Glycogen storage disease type V	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
794359016	Glycogen storage disease, type V (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
92984015	Glycogen storage disease, type V	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
92985019	Myophosphorylase deficiency glycogenosis	en	Synonym	Active	Case insensitive	SNOMED CT core
92986018	McArdle's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
92987010	GSD V	en	Synonym	Active	Case sensitive	SNOMED CT core
92988017	Muscle glycogen phosphorylase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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