Q39.8
Other congenital malformations of esophagus
Billable FY2026 2025-10-01 → 2026-09-30
Instructional notes 3
Q39.8code
Inclusion terms
- Congenital absence of esophagus
- Congenital displacement of esophagus
- Congenital duplication of esophagus
Index entries leading here 9
- Absence (of) (organ or part) (complete or partial)
- esophagus (congenital) Q39.8
- Agenesis
- esophagus Q39.8
- Displacement, displaced
- Cyst (colloid) (mucous) (simple) (retention)
- Duplication, duplex — see also Accessory
- esophagus Q39.8
- Malformation (congenital) — see also Anomaly
- Hypoplasia, hypoplastic
- esophagus (congenital) Q39.8
- Short, shortening, shortness
- esophagus (congenital) Q39.8
- Fusion, fused (congenital)
- trachea and esophagus Q39.8
Alongside this code 8 same parent — Q39
Q39.0 Atresia of esophagus without fistula Q39.1 Atresia of esophagus with tracheo-esophageal fistula Q39.2 Congenital tracheo-esophageal fistula without atresia Q39.3 Congenital stenosis and stricture of esophagus Q39.4 Esophageal web Q39.5 Congenital dilatation of esophagus Q39.6 Congenital diverticulum of esophagus Q39.9 Congenital malformation of esophagus, unspecified
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.