Glycogen storage disease, type I 7265005

SNOMED CT code

SNOMED code

7265005

name

Glycogen storage disease, type I

status

active

date introduced

2002-01-31

fully specified name(s)

Glycogen storage disease, type I (disorder)

synonyms

Glycogen storage disease, type I
Hepatorenal glycogen storage disease
von Gierke's disease
GSD I
Glycogen storage disease, type 1
Liver glycogen disease
von Gierke disease

attributes - group2

Finding site

Liver structure 10200004

attributes - group1

Occurrence

Congenital 255399007

parents

Glycogen storage disease, hepatic form 6075009
Autosomal recessive hereditary disorder 85995004

children

Glucose-6-phosphate transport defect 30102006
Glycogen storage disease type Ia 444707001

hierarchies

a selection of possible paths

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 I 7265005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Glycogen storage disease, type I 7265005

ancestors

sorted most to least specific

Glycogen storage disease, hepatic form 6075009
Autosomal recessive hereditary disorder 85995004
Metabolic and genetic disorder affecting the liver 235903001
Autosomal hereditary disorder 1899006
Glycogen storage disease 29633007
Digestive system hereditary disorder 363080007
Disease of liver 235856003
Disorder of carbohydrate metabolism 20957000
Hereditary disorder by system 363137000
Storage disease 34420000
Disorder of liver and/or biliary tract 1290917001
Liver finding 249565005
Inborn error of metabolism 86095007
Disorder of abdomen 118948005
Abdominal organ finding 249561001
Disorder of digestive organ 76712006
Hereditary metabolic disease 1821000146108
Congenital disease 66091009
Finding of abdomen 609624008
Hereditary disease 32895009
Metabolic disease 75934005
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

Disease 64572001

Metabolic disease 75934005

Metabolic and genetic disorder affecting the liver 235903001

Glycogen storage disease, hepatic form 6075009

Glycogen storage disease, type I 7265005

SNOMED CT code