E74.09

Billable

Other glycogen storage disease

Other glycogen storage disease

Status

Billable / Specific

Block

E70-E88

Parent Code

E74.0

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Andersen disease
  • Glycogen storage disease, types 0, IV, VI-XI
  • Hers disease
  • Liver phosphorylase deficiency
  • Muscle phosphofructokinase deficiency
  • Tauri disease

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(6)
E74.00

Glycogen storage disease, unspecified

BillableE74.01

von Gierke disease

BillableE74.02

Pompe disease

BillableE74.03

Cori disease

BillableE74.04

McArdle disease

BillableE74.05

Lysosome-associated membrane protein 2 [LAMP2] deficiency

Billable
Also Known As / Clinical Terms(457)

SNOMED CT

UMLS

Clinical Terms

  • ANDERSENS DIS
  • glycogenosis type VII
  • GLYCOGENOSIS IV
  • Glycogenosis type VI
  • her's disease
  • Andersen's disease
  • Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome
  • GSDXIII - glycogen storage disease type XIII
  • Type VI, Glycogenosis
  • tarui disease
  • GLYCOGEN STORAGE DISEASE IV
  • Muscle Phosphofructokinase Deficiencies
  • taruis disease
  • Brancher Deficiency
  • Glycogen storage disease, type VII
  • Glycogenosis due to inactive hepatic glycogen phosphorylase
  • tarui's disease
  • AMYLOPECTINOSIS
  • Glycogen phosphorylase kinase deficiency, autosomal recessive
  • Glycogenosis type 9D
  • Glycogenosis viiia
  • Glycogenosis VI
  • Hepatic phosphorylase kinase deficiency
  • Glycogenosis with glucoaminophosphaturia
  • Andersen disease
  • HERS DIS
  • Glycogen Branching Enzyme Deficiency
  • Deficiencies, Muscle Phosphofructokinase
  • Glycogen storage disease type 0
  • Deficiency of amylo-(1,4,6)-transglycosylase
  • Glycogen storage disease type VI
  • Disease, Andersen's
  • glycogenosis type iv
  • Adult polyglucosan body disease
  • Glycogen phosphorylase kinase deficiency
  • Phosphorylase kinase deficiency of liver
  • Glycogen storage disease due to lysosomal associated membrane protein 2 deficiency
  • Phosphate transport defect
  • Polyglucosan body myopathy type 2
  • Glycogen Storage Disease VII
  • Pfkm Deficiencies
  • Glycogen storage disease, type VII (disorder)
  • Glycogen storage disease type 12
  • Hepatic phosphorylase deficiency
  • Deficiency, Pfkm
  • GLYCOGEN STORAGE DIS VI
  • Her Disease
  • Glycogen storage disease type Ic
  • Hers' disease
  • Glycogen storage disease due to liver glycogen synthase deficiency
  • Deficiency, Gbe1
  • Gbe1 Deficiencies
  • GSD7
  • hepatophosphorylase deficiency glycogenosis
  • Glycogenosis due to aldolase A deficiency
  • Glycogenosis 6
  • Hepatic Glycogen Phosphorylase Deficiency
  • MUSCLE PHOSPHOFRUCTOKINASE DEFIC
  • Glycogenosis type 0b
  • glycogen storage disease type iv
  • Polyglucosan body disease adult form
  • Glycogen storage disease type 0b
  • Amylopectinoses
  • Liver Phosphorylase Deficiency Syndrome
  • Brancher Deficiencies
  • gsd iv
  • phosphofructokinase deficiency
  • Glycogen Storage Disease Type 4
  • Disease, Tarui
  • Liver phosphorylase deficiency
  • ANDERSEN DIS
  • Glycogen storage disease type XII
  • Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome
  • Deficiency of 1,4-alpha-glucan branching enzyme (disorder)
  • Glycogen storage disease type IX
  • Deficiencies, Pfkm
  • Type IV Glycogenosis
  • Disease, Tarui's
  • MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY
  • Deficiencies, Brancher
  • Branching-transferase deficiency glycogenosis
  • Glycogen storage disease, muscular form
  • Glycogenosis, type 4
  • Glycogenosis IVs
  • Glycogenosis due to muscle and heart glycogen synthase deficiency
  • GSD type VI
  • TARUIS DIS
  • Hers disease
  • GLYCOGEN STORAGE DIS IV
  • Glycogen storage disease due to lactate dehydrogenase deficiency
  • PGBM1 - polyglucosan body myopathy type 1
  • GSD VI
  • Andersens Disease
  • Deficiency, Muscle Phosphofructokinase
  • Glycogen storage disease due to LAMP-2 deficiency
  • Lysosomal glycogen storage disease with normal acid maltase activity
  • Hepatic and muscle glycogen phosphorylase kinase deficiency
  • Branching enzyme deficiency
  • Glycogen storage disease, type IV
  • Glycogen synthase deficiency
  • Glycogenosis type 0a
  • Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency
  • Glycogenosis 4
  • Pfkm Deficiency
  • glycogenosis type 4
  • Glycogen storage disease due to muscle phosphorylase kinase deficiency
  • Glycogenosis due to LAMP-2 deficiency
  • Glycogenosis type 12
  • Muscle and heart glycogen synthase deficiency
  • Glycogenosis due to inactive phosphorylase
  • PGBM2 - polyglucosan body myopathy type 2
  • Glycogen storage disease, type 7
  • Disease, Hers
  • TARUI DIS
  • 1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency
  • GSD type IV
  • Disease, Andersen
  • Renal glucose-losing syndrome
  • PHK - Hepatic phosphorylase kinase deficiency
  • Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
  • PHOSPHORYLASE DEFICIENCY GLYCOGEN-STORAGE DISEASE OF LIVER
  • GLYCOGEN STORAGE DIS VII
  • Fanconi-Bickel syndrome
  • Hepatic glycogen synthase deficiency
  • Cardiomyopathy due to storage disease
  • GSD4
  • Glycogen storage disease type 8
  • Glycogenosis, type IV
  • Phosphofructokinase Deficiency, Muscle
  • Glycogen storage disease type XI
  • Glycogenosis type 13
  • type iv glycogen storage disease
  • Glycogen storage disease, type 4
  • Glycogen storage disease due to aldolase A deficiency
  • Glycogen storage disease, hepatic form
  • Glycogen storage disease, type VI
  • Glycogen storage disease due to hepatic glycogen synthase deficiency
  • Danon disease
  • Glycogenosis due to phosphoglycerate kinase 1 deficiency
  • GSD6
  • Glycogen storage disease due to muscle beta-enolase deficiency
  • Polyglucosan body myopathy type 1
  • disease tarui
  • Brancher deficiency glycogen storage disease
  • DEFIC BRANCHER
  • Pseudo-phlorizin diabetes
  • Glycogen storage disease type VIII
  • GSD VIII
  • Cardiac glycogen phosphorylase kinase deficiency
  • Glycogen storage disease type 9D
  • Phosphofructokinase Deficiencies, Muscle
  • Glycogen Storage Disease Type VII
  • Tauri disease
  • Glycogen storage disease due to muscle and heart glycogen synthase deficiency
  • Glycogen storage disease type 0a
  • GBE1 DEFICIENCY
  • brancher deficiency glycogenosis
  • Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase
  • Glycogenoses, Type IV
  • Deficiency, Brancher
  • Deficiency of branching enzyme
  • Deficiency of 1,4-alpha-glucan branching enzyme
  • GSDVII
  • brancher glycogen storage disease
  • Glycogen storage disease, types 0, IV, VI-XI
  • BRANCHER DEFIC
  • diseases tarui's
  • Glycogen storage disease type IXB
  • Glycogenosis 4s
  • GSD VII
  • Glycogenosis due to muscle beta-enolase deficiency
  • Deficiencies, Gbe1
  • Glycogenosis 7
  • Muscle enolase deficiency
  • Glycogen storage disease, type IV (disorder)
  • Glycogen storage disease, type VI (disorder)
  • Glycogen storage disease type IXd
  • Glycogen storage disease with hypertrophic cardiomyopathy
  • phosphofructokinase myopathy
  • GLYCOGEN STORAGE DISEASE VI
  • Glycogenosis type XII
  • Andersen glycogenosis
  • Hers glycogenosis
  • Hypertrophic cardiomyopathy due to glycogen storage disease
  • Type IV Glycogenoses
  • Disease, Hers'
  • Hepatic glycogen phosphorylase kinase deficiency
  • DEFIC MUSCLE PHOSPHOFRUCTOKINASE
  • Glycogen storage disease due to muscle pyruvate kinase deficiency
Frequently Asked Questions
What is the ICD-10 code for other glycogen storage disease?

The ICD-10-CM code for other glycogen storage disease is E74.09. The full clinical description is "Other glycogen storage disease". E74.09 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E74.09 mean?

ICD-10-CM code E74.09 represents “Other glycogen storage 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 E74.09 a billable code?

Yes, E74.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E74.09 in?

E74.09 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E74.09?

E74.09 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 E74.09 map to?

E74.09 maps to 30 SNOMED CT concepts: 11179002, 721099001, 297253000, 860839005, 419097006, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E74.09?

E74.09 is linked to 5 UMLS Concept Unique Identifiers: C0017923, C0017926, C0017925, C2874266, C2874267. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E74.09 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other glycogen storage 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 E74.09?

There is no direct ICD-11 mapping available for E74.09 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.