- E71.19 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 E71.19 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E71.19 – other international versions of ICD-10 E71.19 may differ.
ICD-10-CM E71.19 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Hyperleucine-isoleucinemia
- Hypervalinemia
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 E71.19:
- specified NEC > branched-chain amino-acid metabolism E71.2
- hyperleucine-isoleucinemia > Disorder (of)
- hypervalinemia > Disorder (of)
- hyperleucine-isoleucinemia > branched chain E71.2
- hypervalinemia > branched chain E71.2
- other specified > branched chain E71.2
- isoleucine > metabolism NOS E88.9
- leucine > metabolism NOS E88.9
- valine > metabolism NOS E88.9
- leucine-induced > Hypoglycemia (spontaneous) E16.2