E74.09
Other glycogen storage disease
Risk-adjusting (HCC)Billable code
HCC risk adjustment mapping
CMS-HCC V28
HCC50
Amyloidosis, Porphyria, and Other Specified Metabolic Disorders
CMS-HCC ESRD V24
HCC23
Other Significant Endocrine and Metabolic Disorders
RxHCC V08
RXHCC43
Pituitary, Adrenal Gland, and Other Endocrine and Metabolic Disorders
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
This code · E74.09
Synonyms
Andersen disease Glycogen storage disease, types 0, IV, VI-XI Hers disease Liver phosphorylase deficiency Muscle phosphofructokinase deficiency Tauri disease
Inherited from E74Other disorders of carbohydrate metabolism
Inherited from E70-E88Metabolic disorders
Inherited from chapter 4Endocrine, nutritional and metabolic diseases
Excludes 1
transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Official Guidelines for E74.09
FY 2026 ›Find E74.09 in the alphabetic index
23 index paths lead to this code
- Andersen's disease
- Hers' disease
- Tauri's disease
- Deficiency, deficient › glycogen synthetase
- Deficiency, deficient › hepatophosphorylase
- Deficiency, deficient › liver phosphorylase
- Deficiency, deficient › phosphorylase kinase, liver
- Disease, diseased › Andersen's
- Disease, diseased › Hers'
- Disease, diseased › Tauri's
- Deficiency, deficient › muscle › phosphofructokinase
- Disease, diseased › glycogen storage › Andersen's
- Disease, diseased › glycogen storage › hepatorenal
- Disease, diseased › glycogen storage › Hers'
- Disease, diseased › glycogen storage › liver and kidney
- Disease, diseased › glycogen storage › muscle phosphofructokinase
- Disease, diseased › glycogen storage › Tauri's
- Disease, diseased › glycogen storage › type 0
- Disease, diseased › glycogen storage › type IV
- Disease, diseased › glycogen storage › type VI-XI
- Disease, diseased › liver › glycogen storage
- Disorder › metabolism NOS › glycogen storage
- Pyelonephritis › in › glycogen storage disease