Effective from
- Inherited rules changed
Glycogen storage disease
Category — select a more specific code
CDC/NCHS · FY2024Ehlers-Danlos syndromes (Q79.6-)
For US diagnosis claims covered by HIPAA, ICD-10-CM is required from October 1, 2015.
Use the service date for outpatient/professional claims and the discharge date for hospital inpatient claims. Earlier encounters use ICD-9-CM; each individual code must also be valid for the applicable date.
Official coding guidelines → · CMS ↗First observed · 2015-10-01
Latest recorded change · FY2024
Effective from
Glycogen storage disease
Category — select a more specific code
CDC/NCHS · FY2024| All editions | Effective from | Code history |
|---|---|---|
| FY2016 | 2015-10-01 | First observed |
| FY2017 | 2016-10-01 | No tabular change |
| FY2018 | 2017-10-01 | No tabular change |
| FY2019 | 2018-10-01 | No tabular change |
| FY2020 | 2019-10-01 | Inherited rules changed |
| FY2020 · April | 2020-04-01 | No tabular change |
| FY2021 | 2020-10-01 | Inherited rules changed |
| FY2021 · 01-01 | 2021-01-01 | No tabular change |
| FY2022 | 2021-10-01 | Inherited rules changed |
| FY2022 · 04-01 | 2022-04-01 | No tabular change |
| FY2023 | 2022-10-01 | No tabular change |
| FY2023 · 04-01 | 2023-04-01 | No tabular change |
| FY2024 | 2023-10-01 | Inherited rules changed |
| FY2024 · 04-01 | 2024-04-01 | No tabular change |
| FY2025 | 2024-10-01 | No tabular change |
| FY2025 · 04-01 | 2025-04-01 | No tabular change |
| FY2026 | 2025-10-01 | No tabular change |
| FY2026 · April | 2026-04-01 | No tabular change |
| FY2027 | 2026-10-01 | No tabular change |
The official Tabular List has no additional instructions at this code level.
Review the instructions inherited from its parent categories below. Inherited instructions ↓
All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Ehlers-Danlos syndromes (Q79.6-)
E74.00Glycogen storage disease, unspecifiedBillable / specificE74.01von Gierke diseaseBillable / specificE74.02Pompe diseaseBillable / specificE74.03Cori diseaseBillable / specificE74.04McArdle diseaseBillable / specificE74.05Lysosome-associated membrane protein 2 [LAMP2] deficiencyBillable / specificE74.09Other glycogen storage diseaseBillable / specificOther entries in the same category; these are not automatic substitutes.
| Code | Description | Category · further specificity required |
|---|---|---|
| E74.1 | Disorders of fructose metabolism | Category · further specificity required |
| E74.2 | Disorders of galactose metabolism | Category · further specificity required |
| E74.3 | Other disorders of intestinal carbohydrate absorption | Category · further specificity required |
| E74.4 | Disorders of pyruvate metabolism and gluconeogenesis | Billable / specific |
| E74.8 | Other specified disorders of carbohydrate metabolism | Category · further specificity required |
| E74.9 | Disorder of carbohydrate metabolism, unspecified | Billable / specific |
Official titles and instructions are preserved in their source language. Official sources ↗
Code first · glycogen storage disease (E74.0-)
Code first · glycogen storage disease (E74.0-)
Code first · glycogen storage disease (E74.0-)