E75.26

Sulfatase deficiency

Billable / specific

E75.26 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Applicable to

  • Multiple sulfatase deficiency (MSD)

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.

  • adrenoleukodystrophy [Addison-Schilder] (E71.528) (from E75.2)
  • 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)

Also known as

  • Multiple sulfatase deficiency (MSD)
  • Deficiency, deficient, multiple sulfatase
  • Deficiency, deficient, sulfatase
  • MSD

Parent code

  • E75.2Other sphingolipidosisHeader

Related codes

  • E75.21Fabry (-Anderson) diseaseBillable
  • E75.22Gaucher diseaseBillable
  • E75.23Krabbe diseaseBillable
  • E75.24Niemann-Pick diseaseHeader
  • E75.25Metachromatic leukodystrophyBillable
  • E75.27Pelizaeus-Merzbacher diseaseBillable
  • E75.28Canavan diseaseBillable
  • E75.29Other sphingolipidosisBillable

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