- E74.09 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM E74.09 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E74.09 – other international versions of ICD-10 E74.09 may differ.
ICD-10-CM E74.09 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Andersen disease
- Hers disease
- Tauri disease
- Glycogen storage disease, types 0, IV, VI-XI
- Liver phosphorylase deficiency
- Muscle phosphofructokinase deficiency
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 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
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to E74.09:
- glycogen synthetase > Deficiency, deficient
- hepatophosphorylase > Deficiency, deficient
- liver phosphorylase > Deficiency, deficient
- phosphofructokinase > muscle E71.314
- phosphorylase kinase, liver > Deficiency, deficient
- Andersen\’s (glycogenosis IV) > Disease, diseased
- Andersen\’s > glycogen storage E74.00
- hepatorenal > glycogen storage E74.00
- Hers\’ > glycogen storage E74.00
- liver and kidney > glycogen storage E74.00
- muscle phosphofructokinase > glycogen storage E74.00
- Tauri\’s > glycogen storage E74.00
- type 0 > glycogen storage E74.00
- type IV > glycogen storage E74.00
- type VI-XI > glycogen storage E74.00
- Hers\’ (glycogenosis VI) > Disease, diseased
- glycogen storage > liver (chronic) (organic) K76.9
- Tauri\’s > Disease, diseased
- glycogen storage (hepatorenal) > metabolism NOS E88.9
- glycogen storage disease > in (due to) A23.9