1162916008: Glycogen storage disease due to muscle beta-enolase deficiency (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 due to muscle beta-enolase deficiency

\Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency

\Musculoskeletal finding\Disorder of musculoskeletal system\...

\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency

\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency

\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 due to muscle beta-enolase deficiency
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Glycogen storage disease, muscular form\Glycogen storage disease due to muscle beta-enolase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

4592214012 Glycogen storage disease due to muscle beta-enolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

4592215013 Glycogenosis type 13 en Synonym Active Entire term case insensitive SNOMED CT core module

4592216014 Muscle enolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

4592217017 Glycogen storage disease due to muscle beta-enolase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

4592218010 Glycogenosis due to muscle beta-enolase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

4592220013 GSDXIII - glycogen storage disease type XIII en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease due to muscle beta-enolase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Glycogen storage disease due to muscle beta-enolase deficiency	Due to	Deficiency of enolase	true	Inferred relationship	Existential restriction modifier	2
Glycogen storage disease due to muscle beta-enolase deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease due to muscle beta-enolase deficiency	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Glycogen storage disease due to muscle beta-enolase deficiency	Is a	Glycogen storage disease, muscular form	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
4592214012	Glycogen storage disease due to muscle beta-enolase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4592215013	Glycogenosis type 13	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4592216014	Muscle enolase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4592217017	Glycogen storage disease due to muscle beta-enolase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4592218010	Glycogenosis due to muscle beta-enolase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4592220013	GSDXIII - glycogen storage disease type XIII	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module