Q32.1
BillableOther congenital malformations of trachea
Other congenital malformations of trachea
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Atresia of trachea
- Congenital anomaly of tracheal cartilage
- Congenital dilatation of trachea
- Congenital malformation of trachea
- Congenital stenosis of trachea
- Congenital tracheocele
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
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(188)
SNOMED CT
- Congenital absence of trachea3987009
- Congenital diverticulum of trachea5565008
- Congenital dilatation of trachea6296006
- Congenital narrowed trachea9660004
- Congenital stenosis of trachea9660004
- Congenital tracheal stenosis9660004
- Stenosis of trachea11296007
- Tracheal stenosis11296007
- Congenital laryngeal stenosis12070002
- Congenital stenosis of larynx12070002
- Trachea displaced13206009
- Tracheal deviation13206009
- Congenital anomaly of trachea14532008
- Congenital deformity of trachea14532008
- Congenital tracheocele26408002
- Tracheocele33094002
- Absence of bronchus34774005
- Congenital absence of bronchus34774005
- Accessory trachea35555009
- Anomaly of tracheal cartilage42666000
- Congenital anomaly of tracheal cartilage42666000
- Congenital atresia of trachea53189005
- Biliary fistula53206008
- Biliary tract fistula53206008
- Fistula of bile duct53206008
- Perforation of biliary tree with fistula formation53206008
- Atresia of larynx64981002
- Congenital atresia of larynx64981002
- Bronchial stenosis79877004
- Bronchostenosis79877004
- Stenosis of bronchus79877004
- Congenital malposition of trachea93363006
- Congenital malpositioned trachea93363006
- Perforation of trachea95206001
- Tracheal perforation95206001
- Accessory structure of lower respiratory tract123655009
- Agenesis of larynx, trachea and bronchus204533007
- Agenesis of bronchus204534001
- Agenesis of larynx204535000
- Congenital absence of larynx204535000
- Anomaly of laryngeal and tracheal cartilage204537008
- Anomaly of laryngeal and/or tracheal cartilage204537008
- Atresia of larynx and trachea204544004
- Congenital stenosis of larynx, trachea and bronchus204550009
- Congenital bronchial stenosis204551008
- Tracheal fistula233778002
- Congenital tracheal fistula233779005
- Absence of larynx249435003
- No larynx249435003
- Distal origin of brachiocephalic trunk253696009
- Distal origin of innominate artery253696009
- Congenital anomaly of trachea and bronchus253740007
- Congenital malformation of trachea and bronchus253740007
- Tracheobiliary fistula253809007
- Trachea displaced to left271630007
- Neonatal tracheal perforation276547003
- Congenital tracheal collapse397433001
- Congenital stenosis of trachea due to complete rings447810006
- Congenital stenosis of trachea due to tracheal web447811005
- Pig bronchus448412007
- Tracheal origin of right upper lobe bronchus448412007
- True tracheal bronchus448412007
- Distal origin of brachiocephalic artery with tracheal compression449027007
- Congenital tracheobiliary fistula720394008
- Congenital respiratory biliary fistula818951009
- Anomalous tracheobronchial branching890219009
- Congenital anomalous tracheobronchial branching890219009
- Congenital stenosis of the tracheobronchial tree890389003
- Congenital tracheobronchial stenosis890389003
- Agenesis of trachea1003555002
- Developmental duplication cyst of trachea1144251003
- Duplication cyst of trachea1144251003
- Tracheal duplication cyst1144251003
- Deformity of tracheal cartilage1366709001
- Compression of trachea1366717009
- Tracheal compression1366717009
- Congenital malformation of larynx and trachea1085671000119100
UMLS
- Anomaly of tracheal cartilageC0265773
- Congenital anomaly of tracheal cartilageC0265773
- Congenital anomaly of tracheal cartilage (disorder)C0265773
- Atresia of tracheaC0265766
- Congenital Tracheal AtresiaC0265766
- Congenital atresia of tracheaC0265766
- Congenital atresia of trachea (disorder)C0265766
- Tracheal AtresiaC0265766
- Tracheal atresiaC0265766
- Congenital anomaly of tracheaC0265764
- Congenital anomaly of trachea (disorder)C0265764
- Congenital deformity of tracheaC0265764
- Congenital malformation of tracheaC0265764
- Congenital dilatation of tracheaC0265768
- Congenital dilatation of trachea (disorder)C0265768
- Congenital narrowed tracheaC0265767
- Congenital stenosis of tracheaC0265767
- Congenital stenosis of trachea (disorder)C0265767
- Congenital tracheal stenosisC0265767
- Tracheal stenosis, congenitalC0265767
- Congenital tracheoceleC0265759
- Congenital tracheocele (disorder)C0265759
- Other congenital malformations of tracheaC0478016
Clinical Terms
- Tracheobiliary fistula
- Congenital absence of larynx
- Congenital laryngeal stenosis
- Bronchostenosis
- Agenesis of larynx
- Stenosis of trachea
- Atresia of trachea
- Distal origin of brachiocephalic trunk
- Stenosis of bronchus
- Anomaly of laryngeal and tracheal cartilage
- Congenital anomaly of trachea (disorder)
- Congenital bronchial stenosis
- Congenital anomaly of trachea and bronchus
- Congenital atresia of trachea (disorder)
- Anomalous tracheobronchial branching
- Congenital malformation of trachea and bronchus
- Congenital anomaly of tracheal cartilage (disorder)
- Tracheal perforation
- Congenital stenosis of larynx, trachea and bronchus
- Tracheal duplication cyst
- Congenital atresia of larynx
- Congenital absence of trachea
- Congenital tracheal collapse
- Congenital tracheobronchial stenosis
- Congenital stenosis of trachea due to complete rings
- Congenital atresia of trachea
- Congenital tracheal fistula
- Congenital diverticulum of trachea
- Trachea displaced
- True tracheal bronchus
- Distal origin of brachiocephalic artery with tracheal compression
- Congenital respiratory biliary fistula
- Tracheal deviation
- Congenital stenosis of larynx
- Congenital absence of bronchus
- Congenital tracheobiliary fistula
- Agenesis of trachea
- Accessory structure of lower respiratory tract
- Anomaly of tracheal cartilage
- Agenesis of larynx, trachea and bronchus
- Absence of bronchus
- Distal origin of innominate artery
- Congenital tracheocele (disorder)
- Congenital tracheal stenosis
- No larynx
- Perforation of trachea
- Duplication cyst of trachea
- Congenital malformation of larynx and trachea
- Congenital tracheocele
- Deformity of tracheal cartilage
- Congenital dilatation of trachea
- Congenital deformity of trachea
- Congenital malposition of trachea
- Neonatal tracheal perforation
- Trachea displaced to left
- Congenital stenosis of trachea due to tracheal web
- Congenital stenosis of the tracheobronchial tree
- Atresia of larynx
- Biliary tract fistula
- Congenital stenosis of trachea (disorder)
- Tracheal stenosis, congenital
- Atresia of larynx and trachea
- Bronchial stenosis
- Tracheal compression
- Congenital anomaly of tracheal cartilage
- Congenital stenosis of trachea
- Biliary fistula
- Tracheal fistula
- Tracheal stenosis
- Compression of trachea
- Tracheal Atresia
- Agenesis of bronchus
- Congenital anomaly of trachea
- Fistula of bile duct
- Congenital anomalous tracheobronchial branching
- Congenital malformation of trachea
- Developmental duplication cyst of trachea
- Congenital narrowed trachea
- Tracheocele
- Congenital malpositioned trachea
- Pig bronchus
- Tracheal origin of right upper lobe bronchus
- Absence of larynx
- Perforation of biliary tree with fistula formation
- Accessory trachea
- Congenital dilatation of trachea (disorder)
- Anomaly of laryngeal and/or tracheal cartilage
- Congenital Tracheal Atresia
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of trachea?
The ICD-10-CM code for other congenital malformations of trachea is Q32.1. The full clinical description is "Other congenital malformations of trachea". Q32.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q32.1 mean?
ICD-10-CM code Q32.1 represents “Other congenital malformations of trachea”. 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 Q32.1 a billable code?
Yes, Q32.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q32.1 in?
Q32.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q32.1?
Q32.1 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital bronchiectasis (Q33.4).
What SNOMED CT codes does Q32.1 map to?
Q32.1 maps to 49 SNOMED CT concepts: 34774005, 249435003, 123655009, 35555009, 204534001, and 44 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q32.1?
Q32.1 is linked to 7 UMLS Concept Unique Identifiers: C0265773, C0265766, C0265764, C0265768, C0265767, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q32.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of trachea affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q32.1?
Q32.1 maps to the ICD-11 code: LA73.Z (Structural developmental anomalies of trachea, unspecified).
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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.