Glycogen storage disease type III 66937008

SNOMED CT code

SNOMED code

66937008

name

Glycogen storage disease type III

status

active

date introduced

2002-01-31

fully specified name(s)

Glycogen storage disease, type III (disorder)

synonyms

Glycogen storage disease, type III
Cori's disease
Amylo-1,6-glucosidase deficiency
Debrancher deficiency glycogen storage disease
Limit dextrinosis
GSD III
Glycogen storage disease type 3
Cori disease
Debrancher enzyme deficiency
Limit dextrin - glycogen
Glycogen storage disease type III

attributes - group2

Occurrence

Congenital 255399007

attributes - group3

Finding site

Skeletal muscle structure 127954009

attributes - group1

Finding site

Liver structure 10200004

parents

Glycogen storage disease, muscular form 15978003
Glycogen storage disease, hepatic form 6075009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Glycogen storage disease, muscular form 15978003
Glycogen storage disease type III 66937008

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Metabolic disease 75934005
Metabolic and genetic disorder affecting the liver 235903001
Glycogen storage disease, hepatic form 6075009
Glycogen storage disease type III 66937008

ancestors

sorted most to least specific

Glycogen storage disease, muscular form 15978003
Glycogen storage disease, hepatic form 6075009
Metabolic myopathy 26111005
Metabolic and genetic disorder affecting the liver 235903001
Glycogen storage disease 29633007
Hereditary disorder of musculoskeletal system 363212003
Digestive system hereditary disorder 363080007
Disorder of skeletal muscle 75047002
Disease of liver 235856003
Disorder of carbohydrate metabolism 20957000
Hereditary disorder by system 363137000
Storage disease 34420000
Disorder of muscle 129565002
Disorder of liver and/or biliary tract 1290917001
Disorder of soft tissue 19660004
Disorder of musculoskeletal system 928000
Liver finding 249565005
Inborn error of metabolism 86095007
Muscle finding 106030000
Disorder of abdomen 118948005
General finding of soft tissue 248402002
Musculoskeletal finding 106028002
Abdominal organ finding 249561001
Disorder of digestive organ 76712006
Hereditary metabolic disease 1821000146108
Congenital disease 66091009
Finding of abdomen 609624008
Metabolic disease 75934005
Hereditary disease 32895009
Viscus structure finding 406123005
Disorder of digestive system 53619000
Disorder of abdominopelvic segment of trunk 822988000
Finding of abdominopelvic segment of trunk 822987005
Genetic disease 782964007
Disorder of body system 362965005
Disorder of trunk 128121009
Digestive system finding 386617003
Finding of trunk structure 302292003
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Musculoskeletal finding 106028002

Disorder of musculoskeletal system 928000

Hereditary disorder of musculoskeletal system 363212003

Glycogen storage disease, muscular form 15978003

Glycogen storage disease type III 66937008

SNOMED CT code