Esophageal atresia

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Esophageal atresia

ORPHA:1199Morphological anomaly

Also called CEA · Congenital esophageal atresia · EA/TEF · Esophageal atresia with or without trachea-esophageal fistula · Oesophageal atresia

What it is

A rare congenital malformation characterized by an interruption in the continuity of the esophagus, with or without persistent communication with the trachea. The clinical presentation varies according to the anatomy, and can lead to the inability to swallow or, in the most severe cases, respiratory distress.

Key facts

Prevalence
1-5 / 10 000 (Europe)
Age of onset
Neonatal
Inheritance
Not applicable
Classified as
Morphological anomaly

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

ICD-10 codes

Q39.0ICD-10 uses a narrower term
Q39.1ICD-10 uses a narrower term

Cross-references

GARD 6381MEDDRA 10030146MESH D004933OMIM 189960UMLS C0014850

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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