E75.0

GM2 gangliosidosis

Non-billable header

E75.0 is a non-billable header code. Use one of the more specific codes below.

Inclusion terms

Includes (from E75)

  • 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.

Excludes1

Not coded here — never report together with this code.

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E75)
  • androgen insensitivity syndrome (E34.5-) (from E75)
  • congenital adrenal hyperplasia (E25.0) (from E75)
  • hemolytic anemias attributable to enzyme disorders (D55.-) (from E75)
  • Marfan syndrome (Q87.4-) (from E75)
  • 5-alpha-reductase deficiency (E29.1) (from E75)
  • mucolipidosis, types I-III (E77.0-E77.1) (from E75)
  • Refsum's disease (G60.1) (from E75)

Excludes2

Not included here — may be reported together when both conditions exist.

  • Ehlers-Danlos syndromes (Q79.6-) (from E75)

Parent code

  • E75Disorders of sphingolipid metabolism and other lipid storage disordersHeader

More specific codes E75.0

  • E75.00GM2 gangliosidosis, unspecifiedBillable
  • E75.01Sandhoff diseaseBillable
  • E75.02Tay-Sachs diseaseBillable
  • E75.09Other GM2 gangliosidosisBillable

Related codes

  • E75.1Other and unspecified gangliosidosisHeader
  • E75.2Other sphingolipidosisHeader
  • E75.3Sphingolipidosis, unspecifiedBillable
  • E75.4Neuronal ceroid lipofuscinosisBillable
  • E75.5Other lipid storage disordersBillable
  • E75.6Lipid storage disorder, unspecifiedBillable

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