- Q61.19 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 Q61.19 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q61.19 – other international versions of ICD-10 Q61.19 may differ.
ICD-10-CM Q61.19 is grouped within Diagnostic Related Group(s):
- 698 Other kidney and urinary tract diagnoses with mcc
- 699 Other kidney and urinary tract diagnoses with cc
- 700 Other kidney and urinary tract diagnoses without cc/mcc
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 Q61.19:
- infantile type NEC > specified as polycystic Q61.3
- infantile type NEC (autosomal recessive) > specified as polycystic Q61.3
- infantile type NEC > kidney (congenital) Q61.9
- infantile type NEC (autosomal recessive) > polycystic Q61.3
- childhood type NEC > polycystic Q61.3
- childhood type NEC > kidney or renal Q61.3
- childhood type NEC > polycystic (congenital) Q61.3
- recessive NEC > autosomal Q61.2
- childhood type NEC > polycystic Q61.3
- infantile type NEC > polycystic Q61.3
- autosomal recessive NEC (infantile type) > degeneration, kidney Q61.3
- recessive NEC > autosomal Q61.2
- autosomal recessive NEC (childhood type) > kidney Q61.3
- infantile type NEC > kidney Q61.3