- E72.81 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 E72.81 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E72.81 – other international versions of ICD-10 E72.81 may differ.
ICD-10-CM E72.81 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- 4-hydroxybutyric aciduria
- Disorders of GABA metabolism
- GABA metabolic defect
- GABA transaminase deficiency
- GABA-T deficiency
- Gamma-hydroxybutyric aciduria
- SSADHD
- Succinic semialdehyde dehydrogenase deficiency
Code History
- 2019 (effective 10/1/2018): New code
- 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 E72.81:
- 4-hydroxybutyric > Aciduria
- gamma-hydroxybutyric > Aciduria
- GABA metabolic (gamma aminobutyric acid) > Defect, defective Q89.9
- GABA transaminase (gamma aminobutyric acid) > Deficiency, deficient
- GABA-T (gamma aminobutyric acid transaminase) > Deficiency, deficient
- succinic semialdehyde dehydrogenase > Deficiency, deficient
- gamma aminobutyric acid metabolism (GABA) > Disorder (of)