Q33.0 is the ICD-10 code for Congenital cystic lung. It is a four-character subcategory of Q33 (Congenital malformations of lung), the most specific level in the WHO edition. It belongs to the block Q30–Q34 (Congenital malformations of the respiratory system) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.
- Code type
- Subcategory (4 characters)
- Chapter
- XVII · Q00–Q99
- Classification
- WHO ICD-10, 2019 version
What Q33.0 includes
Conditions and terms that are coded here.
- Congenital:
- honeycomb lung
- lung disease: cystic
- lung disease: polycystic
What Q33.0 excludes
Conditions that look similar but belong under another code.
- cystic lung disease, acquired or unspecified J98.4
Q33.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q33.0Medfödd cystlunga
Q33.0Medfødt cystelunge
DQ330Cystelunge
- DQ330AMedfødt bronkogen cyste
Q33.0Synnynnäinen kystinen keuhko
- Q33.00Synnynnäinen yksittäinen keuhkokysta
- Q33.01Keuhkojen (synnynnäinen) monirakkulatauti
- Q33.02Synnynnäinen hunajakennokeuhko
- Q33.08Muu synnynnäinen kystinen keuhko
Q33.0Angeborene Zystenlunge
Q33.0Poumon kystique congénital
Q33.0congenitale cystenlong
Q33.0Congenital cystic lung
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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