- Q33.0 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 Q33.0 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q33.0 – other international versions of ICD-10 Q33.0 may differ.
ICD-10-CM Q33.0 is grouped within Diagnostic Related Group(s):
Applicable To
- Congenital cystic lung disease
- Congenital honeycomb lung
- Congenital polycystic lung disease
Type 1 Excludes
- cystic fibrosis (E84.0)
- cystic lung disease, acquired or unspecified (J98.4)
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 Q33.0:
- congenital > bronchogenic (mediastinal) (sequestration) J98.4
- lung > congenital NEC Q89.8
- congenital > lung J98.4
- congenital > lung disease J98.4
- congenital > lung J98.4
- congenital > cystic J98.4
- congenital > polycystic J98.4
- congenital > lung or pulmonary J98.4
- congenital > Honeycomb lung J98.4
- congenital > lung J98.4