Glycogen storage disease
- E74.0 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- The 2025 edition of ICD-10-CM E74.0 became effective on October 1, 2024.
- This is the American ICD-10-CM version of E74.0 – other international versions of ICD-10 E74.0 may differ.
The following code(s) above E74.0 contain annotation back-references
that may be applicable to E74.0:
- E00-E89 Endocrine, nutritional and metabolic diseases
- E70-E88 Metabolic disorders
- E74 Other disorders of carbohydrate metabolism
Clinical Information
- A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
- An inherited metabolic disorder characterized either by defects in glycogen synthesis or defects in the breaking down of glycogen. It results either in the creation of abnormal forms of glycogen or accumulation of glycogen in the tissues.
- Any of a group of metabolic disorders characterized by excessive storage of glycogen.
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- 2024 (effective 10/1/2023): No change
- 2025 (effective 10/1/2024): No change
Code annotations containing back-references to E74.0:
- Code First: N16, G73.7, I43