E75.09

Other GM2 gangliosidosis

Risk-adjusting (HCC)Billable code

HCC risk adjustment mapping

CMS-HCC ESRD V24

HCC52

Dementia Without Complication

RxHCC V08

RXHCC41

Lysosomal Storage Disorders

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

This code · E75.09
Synonyms

Adult GM2 gangliosidosis Juvenile GM2 gangliosidosis

Inherited from E75Disord of sphingolipid metab and oth lipid storage disorders
Excludes 1

mucolipidosis, types I-III (E77.0-E77.1) Refsum's disease (G60.1)

Inherited from E70-E88Metabolic disorders
Excludes 1

androgen insensitivity syndrome (E34.5-) congenital adrenal hyperplasia (E25.0) hemolytic anemias attributable to enzyme disorders (D55.-) Marfan syndrome (Q87.4-) 5-alpha-reductase deficiency (E29.1)

Excludes 2

Ehlers-Danlos syndromes (Q79.6-)

Inherited from chapter 4Endocrine, nutritional and metabolic diseases
Excludes 1

transitory endocrine and metabolic disorders specific to newborn (P70-P74)

Note

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.

Official Guidelines for E75.09

FY 2026 ›
I.C.4Chapter-specific guidanceChapter 4: Endocrine, Nutritional, and Metabolic Diseases (E00-E89)

Subsections

Find E75.09 in the alphabetic index

1 index path leads to this code