- E76.29 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 E76.29 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E76.29 – other international versions of ICD-10 E76.29 may differ.
ICD-10-CM E76.29 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- beta-Glucuronidase deficiency
- Maroteaux-Lamy (mild) (severe) syndrome
- Mucopolysaccharidosis, types VI, VII
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 E76.29:
- beta-glucuronidase > Deficiency, deficient
- beta-gluduronidase deficiency > Mucopolysaccharidosis E76.3
- Maroteaux-Lamy syndrome > Mucopolysaccharidosis E76.3
- specified NEC > Mucopolysaccharidosis E76.3
- VI > type
- VII > type