Q33.0
BillableCongenital cystic lung
Congenital cystic lung
Status
Billable / Specific
Parent Code
Q33Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital cystic lung disease
- Congenital honeycomb lung
- Congenital polycystic lung disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Congenital honeycomb lung59128005
- Congenital cystic disease of lung87119009
- Congenital cystic lung87119009
- Congenital polycystic disease of lung87119009
- Congenital polycystic lung87119009
- Multiple congenital bronchogenic cysts87119009
- CPAM - Congenital pulmonary airway malformation111318005
- Congenital cystic adenomatoid malformation of lung111318005
- Congenital cystic adenomatoid malformation of the lung111318005
- Congenital pulmonary airway malformation111318005
- Cyst of lung275504005
- Lung cyst275504005
- Multiple cysts of lung275505006
- Multiple lung cysts275505006
- Nephroblastoma302849000
- Wilm's tumor302849000
- Wilms tumor302849000
- Wilms tumour302849000
- Congenital bronchogenic cyst762195006
- GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome782722002
- GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome782722002
- GLOW syndrome782722002
- Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome782722002
- Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome782722002
- Congenital pulmonary airway malformation type 4890388006
- Congenital pulmonary airway malformation type 2890390007
- Congenital pulmonary airway malformation type 3890391006
- Congenital pulmonary airway malformation type 1890392004
- Congenital pulmonary airway malformation type 0890394003
UMLS
- Congenital cystic disease of lungC0158641
- Congenital cystic lungC0158641
- Congenital cystic lung (disorder)C0158641
- Congenital cystic lung diseaseC0158641
- Congenital lung cystC0158641
- Cystic lung, congenitalC0158641
- congenital cystic lungC0158641
- congenital lung cystC0158641
- congenital lung cystsC0158641
- Congenital honeycomb lungC0265779
- Congenital honeycomb lung (disorder)C0265779
- Congenital polycystic disease of lungC0555213
- Congenital polycystic lungC0555213
- Congenital polycystic lung diseaseC0555213
- Multiple congenital bronchogenic cystsC0555213
Frequently Asked Questions
What is the ICD-10 code for congenital cystic lung?
The ICD-10-CM code for congenital cystic lung is Q33.0. The full clinical description is "Congenital cystic lung". Q33.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q33.0 mean?
ICD-10-CM code Q33.0 represents "Congenital cystic lung". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q33.0 a billable code?
Yes, Q33.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q33.0 in?
Q33.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q33.0?
Q33.0 has Excludes1 notes indicating codes that cannot be used together with it, including: cystic fibrosis (E84.0); cystic lung disease, acquired or unspecified (J98.4).
What SNOMED CT codes does Q33.0 map to?
Q33.0 maps to 13 SNOMED CT concepts: 111318005, 762195006, 87119009, 59128005, 890394003, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q33.0?
Q33.0 is linked to 3 UMLS Concept Unique Identifiers: C0158641, C0265779, C0555213. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.