E74.01
Billablevon Gierke disease
von Gierke disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Type I glycogen storage disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •diabetes mellitusE08-E13
- •hypoglycemia NOSE16.2
- •increased secretion of glucagonE16.3
- •mucopolysaccharidosisE76.0-E76.3
Related Codes(6)
Also Known As / Clinical Terms(132)
SNOMED CT
- Glycogen storage disease, hepatic form6075009
- GSD I7265005
- Glycogen storage disease, type 17265005
- Glycogen storage disease, type I7265005
- Hepatorenal glycogen storage disease7265005
- Liver glycogen disease7265005
- von Gierke disease7265005
- von Gierke's disease7265005
- Glucose 6-phosphate transport defect30102006
- Glucose-6-phosphate transport defect30102006
- Glycogen storage disease type Ib30102006
- Deficiency of glucose-6-phosphatase124437004
- Glucose transport defect237966006
- Glycogen storage disease type Id237966006
- Glycogen storage disease type Ia444707001
UMLS
- DEFIC GLUCOSEPHOSPHATASEC0017920
- Deficiencies, Glucose-6-PhosphataseC0017920
- Deficiencies, GlucosephosphataseC0017920
- Deficiency of glucose-6-phosphataseC0017920
- Deficiency of glucose-6-phosphatase (disorder)C0017920
- Deficiency, Glucose-6-PhosphataseC0017920
- Deficiency, GlucosephosphataseC0017920
- Disease, GierkeC0017920
- Disease, Gierke'sC0017920
- Disease, von GierkeC0017920
- Disease, von Gierke'sC0017920
- GIERKE DISC0017920
- GIERKES DISC0017920
- GLUCOSE 6 PHOSPHATASE DEFICC0017920
- GLUCOSEPHOSPHATASE DEFICC0017920
- GLYCOGEN STORAGE DIS IC0017920
- GSD IC0017920
- GSD type IC0017920
- Gierke DiseaseC0017920
- Gierke's DiseaseC0017920
- Gierkes DiseaseC0017920
- Glucose 6 Phosphatase DeficiencyC0017920
- Glucose-6-Phosphatase DeficienciesC0017920
- Glucose-6-Phosphatase DeficiencyC0017920
- Glucose-6-phosphatase deficiencyC0017920
- Glucosephosphatase DeficienciesC0017920
- Glucosephosphatase DeficiencyC0017920
- Glycogen Storage Disease 1 (GSD I)C0017920
- Glycogen Storage Disease Type IC0017920
- Glycogen storage disease type IC0017920
- Glycogen storage disease, type 1C0017920
- Glycogen storage disease, type IC0017920
- Glycogen storage disease, type I (disorder)C0017920
- Glycogenosis 1C0017920
- HEPATORENAL GLYCOGEN STORAGE DISC0017920
- Hepatorenal Glycogen Storage DiseaseC0017920
- Hepatorenal form of glycogen storage diseaseC0017920
- Hepatorenal glycogen storage diseaseC0017920
- Hepatorenal glycogenosisC0017920
- Liver glycogen diseaseC0017920
- Type I glycogen storage diseaseC0017920
- Von Gierke diseaseC0017920
- Von Gierke's diseaseC0017920
- disease glycogen i storage typeC0017920
- diseases gierke's vonC0017920
- gierke's diseaseC0017920
- glucose 6 phosphatase deficiencyC0017920
- glucose-6-phosphatase deficiencyC0017920
- glycogen storage disease iC0017920
- glycogen storage disease type IC0017920
- glycogen storage disease type iC0017920
- glycogenosis type IC0017920
- glycogenosis type iC0017920
- hepatorenal glycogen storage diseaseC0017920
- hepatorenal glycogenosisC0017920
- i glycogen storage diseaseC0017920
- type i glycogen storage diseaseC0017920
- von Gierke DiseaseC0017920
- von Gierke diseaseC0017920
- von Gierke's DiseaseC0017920
- von Gierke's diseaseC0017920
- von Gierkes DiseaseC0017920
- von gierke diseaseC0017920
- von gierke's diseaseC0017920
- von gierkes diseaseC0017920
Clinical Terms
- Glycogen storage disease, type 1
- Deficiency, Glucose-6-Phosphatase
- Deficiencies, Glucosephosphatase
- Liver glycogen disease
- Gierke's Disease
- Deficiency of glucose-6-phosphatase
- Glycogen storage disease type Ib
- Deficiency of glucose-6-phosphatase (disorder)
- Glucosephosphatase Deficiency
- Glycogen Storage Disease Type I
- Glycogen storage disease type Id
- Glycogen Storage Disease 1 (GSD I)
- disease glycogen i storage type
- Glucose 6 Phosphatase Deficiency
- HEPATORENAL GLYCOGEN STORAGE DIS
- Type I glycogen storage disease
- von gierke's disease
- Glucosephosphatase Deficiencies
- Deficiency, Glucosephosphatase
- Disease, Gierke's
- Glucose-6-phosphate transport defect
- von Gierkes Disease
- glycogenosis type I
- Glucose 6-phosphate transport defect
- Glycogen storage disease, type I
- Disease, von Gierke
- GSD I
- glycogen storage disease i
- hepatorenal glycogenosis
- Hepatorenal Glycogen Storage Disease
- Gierkes Disease
- Glucose-6-Phosphatase Deficiencies
- Glucose-6-phosphatase deficiency
- Glycogen storage disease, type I (disorder)
- Glycogen storage disease type Ia
- diseases gierke's von
- Glycogen storage disease, hepatic form
- Disease, Gierke
- i glycogen storage disease
- GIERKES DIS
- Glycogenosis 1
- Deficiencies, Glucose-6-Phosphatase
- Disease, von Gierke's
- GLUCOSEPHOSPHATASE DEFIC
- GLUCOSE 6 PHOSPHATASE DEFIC
- GIERKE DIS
- GSD type I
- Glucose transport defect
- Gierke Disease
- Hepatorenal form of glycogen storage disease
- DEFIC GLUCOSEPHOSPHATASE
- GLYCOGEN STORAGE DIS I
Frequently Asked Questions
What is the ICD-10 code for von gierke disease?
The ICD-10-CM code for von gierke disease is E74.01. The full clinical description is "von Gierke disease". E74.01 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.01 mean?
ICD-10-CM code E74.01 represents “von Gierke disease”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E74.01 a billable code?
Yes, E74.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.01 in?
E74.01 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.01?
E74.01 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 7 more.
What SNOMED CT codes does E74.01 map to?
E74.01 maps to 6 SNOMED CT concepts: 124437004, 7265005, 30102006, 237966006, 444707001, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.01?
E74.01 is linked to 1 UMLS Concept Unique Identifier: C0017920. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.01 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like von gierke disease affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E74.01?
There is no direct ICD-11 mapping available for E74.01 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.