274864009: Glycogen storage disease, type II (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\...

\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, type II (disorder)

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Glycogen storage disease, type II (disorder)

\Metabolic disease\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, type II (disorder)
\Metabolic disease\Disorder of carbohydrate metabolism\Glycogen storage disease\Glycogen storage disease, type II (disorder)

\Congenital disease (disorder)\Inborn error of metabolism\Storage disease\Glycogen storage disease\Glycogen storage disease, type II (disorder)

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

410733010 Glycogen heart disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

667668013 Glycogen storage disease, type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2765038013 Glycogen storage disease, type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3297533010 Pompe's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3297616011 Pompe disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3331980017 Glycogen storage disease due to acid maltase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3331981018 Alpha-1,4-glucosidase acid deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3331982013 Glycogenosis due to acid maltase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3331983015 Glycogenosis type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3331984014 Glycogen storage disease due to acid maltase deficiency (AMD) is an autosomal recessive trait leading to metabolic myopathy that affects cardiac and respiratory muscles in addition to skeletal muscle and other tissues. AMD represents a wide spectrum of clinical presentations caused by an accumulation of glycogen in lysosomes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3443391000052110 generaliserad glykogeninlagringssjukdom hos spädbarn sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

3851721000052119 Pompes sjukdom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Glycogen storage disease, type II (disorder)	Is a	Glycogen storage disease	true	Inferred relationship	Some
Glycogen storage disease, type II (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Glycogen storage disease, type II (disorder)	Finding site	Skeletal muscle structure	false	Inferred relationship	Some
Glycogen storage disease, type II (disorder)	Finding site	Liver structure	false	Inferred relationship	Some
Glycogen storage disease, type II (disorder)	Is a	Glycogen storage disease, muscular form	false	Inferred relationship	Some
Glycogen storage disease, type II (disorder)	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Glycogen storage disease due to acid maltase deficiency, infantile onset	Is a	True	Glycogen storage disease, type II (disorder)	Inferred relationship	Some
Glycogen storage disease type II late onset (disorder)	Is a	True	Glycogen storage disease, type II (disorder)	Inferred relationship	Some
Enzyme replacement therapy in lysosomal alpha-1,4-glucosidase deficiency - infantile onset (Pompe disease) (procedure)	Has focus	True	Glycogen storage disease, type II (disorder)	Inferred relationship	Some	2

This concept is not in any reference sets