Other congenital malformations of esophagus
Billable / specificPOA exempt
Q39.8 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Congenital absence of esophagus
- Congenital displacement of esophagus
- Congenital duplication of esophagus
Includes (from Q39)
- Note: Codes from this chapter are not for use on maternal records
Excludes2
Not included here — may be reported together when both conditions exist.
Also known as
- Congenital absence of esophagus
- Congenital displacement of esophagus
- Congenital duplication of esophagus
- Absence, esophagus
- Agenesis, esophagus
- Cyst, congenital NEC, esophagus
- Displacement, displaced, esophageal mucosa into cardia of stomach, congenital
- Displacement, displaced, esophagus, congenital
- Duplication, duplex, esophagus
- Fusion, fused, trachea and esophagus
- Hypoplasia, hypoplastic, esophagus
- Malformation, esophagus, specified type NEC
- Short, shortening, shortness, esophagus
Parent code
- Q39Congenital malformations of esophagusHeader
Related codes
- Q39.0Atresia of esophagus without fistulaBillable
- Q39.1Atresia of esophagus with tracheo-esophageal fistulaBillable
- Q39.2Congenital tracheo-esophageal fistula without atresiaBillable
- Q39.3Congenital stenosis and stricture of esophagusBillable
- Q39.4Esophageal webBillable
- Q39.5Congenital dilatation of esophagusBillable
- Q39.6Congenital diverticulum of esophagusBillable
- Q39.9Congenital malformation of esophagus, unspecifiedBillable