- E72.3 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 E72.3 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E72.3 – other international versions of ICD-10 E72.3 may differ.
ICD-10-CM E72.3 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Glutaric aciduria NOS
- Glutaric aciduria (type I)
- Hydroxylysinemia
- Hyperlysinemia
Type 1 Excludes
- glutaric aciduria type II (E71.313)
- Refsum’s disease (G60.1)
- Zellweger syndrome (E71.510)
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 E72.3:
- pipecolic > Acidemia E87.20
- glutaric (type I) > Aciduria
- lysine and hydroxylysine metabolism > Disorder (of)
- hydroxylysine > amino-acid E72.9
- lysine > amino-acid E72.9
- hydroxylysine > metabolism E88.9
- lysine > metabolism E88.9
- lysine > Hyperaminoaciduria
- lysine > Intolerance