E74.02

Billable

Pompe disease

Pompe disease

Status

Billable / Specific

Block

E70-E88

Parent Code

E74.0

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Cardiac glycogenosis
  • Type II glycogen storage 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

BillableE74.03

Cori disease

BillableE74.04

McArdle disease

BillableE74.05

Lysosome-associated membrane protein 2 [LAMP2] deficiency

BillableE74.09

Other glycogen storage disease

Billable
Also Known As / Clinical Terms(206)

SNOMED CT

UMLS

Clinical Terms

  • Lysosomal alpha-1,4-Glucosidase Deficiency Disease
  • Glycogenosis type II, infantile onset
  • Lysosomal storage disease
  • Deficiency of alpha-glucosidase
  • Fatal congenital nonlysosomal heart glycogenosis
  • Glycogenosis type II
  • Deficiency of amyloglucosidase
  • Glycogen storage disease type II
  • Acid Maltase Deficiency Disease
  • DEFIC DIS LYSOSOMAL ALPHA 1 4 GLUCOSIDASE
  • Deficiencies, GAA
  • Acid Alpha-Glucosidase Deficiency
  • Infiltrative cardiomyopathy
  • Glycogen storage disease type 15
  • GAA DEFICIENCY
  • Acid Alpha-Glucosidase Deficiencies
  • Deficiency of glucoinvertase
  • GLYCOGEN STORAGE DIS II
  • Glycogenosis 2
  • Alpha-1,4-glucosidase acid deficiency, late onset
  • Glycogen Storage Disease II
  • ACID MALTASE DEFICIENCY
  • pompe's disease
  • Deficiency, Acid Alpha-Glucosidase
  • disease pompe's
  • Glycogen storage disease due to acid maltase deficiency, late-onset
  • Deficiencies, Acid Alpha-Glucosidase
  • Pompe disease, late onset
  • generalized glycogenosis
  • AMD
  • Deficiency of gamma-amylase
  • Alpha-Glucosidase Deficiencies, Acid
  • GAA Deficiencies
  • ALPHA-1,4-GLUCOSIDASE DEFICIENCY
  • Glycogen storage disease type XV
  • Deficiency of maltase
  • Glycogen storage disease type II infantile onset
  • Alpha-1,4-glucosidase acid deficiency
  • Glycogenosis due to acid maltase deficiency
  • Pompe disease, infantile onset
  • POMPE DIS
  • maltase acid deficiency
  • Deficiency of glucan 1,4-alpha-glucosidase
  • alpha 1,4 glucosidase deficiency
  • LYSOSOMAL ALPHA 1 4 GLUCOSIDASE DEFIC DIS
  • ACID MALTASE DEFIC DIS
  • Glycogen storage disease type II late onset
  • Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
  • Disease, Pompe's
  • maltase deficiency
  • Deficiency of acid maltase
  • Cardiac glycogenosis (disorder)
  • Glycogen Storage Disease Type 2
  • 2 glycogenosis
  • Alpha-Glucosidase Deficiency
  • Type IIs, Glycogenosis
  • Glycogenosis, Generalized
  • Glycogen heart disease
  • GSD II
  • GSD2s
  • Glycogen storage disease due to acid maltase deficiency, infantile onset
  • Alpha-Glucosidase Deficiency, Acid
  • Cardiac glycogenosis
  • GSD2
  • Glycogen storage disease due to acid maltase deficiency (disorder)
  • Glycogenosis due to acid maltase deficiency, infantile onset
  • Glycogen storage disease, type II
  • Alpha-Glucosidase Deficiencies
  • Glycogenoses, Generalized
  • Glycogenosis type II, late onset
  • Deficiency Disease, Lysosomal alpha-1,4-Glucosidase
  • Deficiency of glucoamylase
  • Deficiency of glucosidosucrase
  • Glycogen storage disease due to acid maltase deficiency
  • pompes disease
  • Deficiency, GAA
  • Deficiency Disease, Acid Maltase
  • DEFIC DIS ACID MALTASE
  • Acid Alpha Glucosidase Deficiency
  • Disease, Pompe
  • Deficiency of Alpha Glucosidase
  • Type II, Glycogenosis
  • Generalized Glycogenoses
  • Lysosomal alpha 1,4 Glucosidase Deficiency Disease
  • Type II glycogen storage disease
  • Deficiency of exo-1,4-alpha-glucosidase
  • POMPES DIS
  • Glycogenosis with severe cardiomyopathy due to glycogenin deficiency
Frequently Asked Questions
What is the ICD-10 code for pompe disease?

The ICD-10-CM code for pompe disease is E74.02. The full clinical description is "Pompe disease". E74.02 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E74.02 mean?

ICD-10-CM code E74.02 represents “Pompe 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 E74.02 a billable code?

Yes, E74.02 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E74.02 in?

E74.02 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E74.02?

E74.02 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 E74.02 map to?

E74.02 maps to 10 SNOMED CT concepts: 274864009, 722343009, 195025008, 124454007, 124462004, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E74.02?

E74.02 is linked to 2 UMLS Concept Unique Identifiers: C0017921, C0340420. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E74.02 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like pompe 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 E74.02?

There is no direct ICD-11 mapping available for E74.02 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.