- Q92.9 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 Q92.9 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q92.9 – other international versions of ICD-10 Q92.9 may differ.
ICD-10-CM Q92.9 is grouped within Diagnostic Related Group(s):
- 951 Other factors influencing health status
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 Q92.9:
- chromosome (s) NEC (nonsex) > Accessory (congenital)
- partial > chromosome (s) NEC (nonsex) Q92.9
- trisomy > Syndrome
- autosomes > Trisomy (syndrome) Q92.9
- whole chromosome > Trisomy (syndrome) Q92.9
- partial > whole chromosome Q92.9