GTR Home > Conditions/Phenotypes > Fanconi anemia, complementation group B


Excerpted from the GeneReview: Esophageal Atresia/Tracheoesophageal Fistula Overview
Esophageal atresia (EA) is a developmental defect of the upper gastrointestinal tract in which the continuity between the upper and lower esophagus is lost. EA can occur with or without tracheoesophageal fistula (TEF), an abnormal connection between the trachea and the esophagus.

Genes See tests for all associated and related genes

  • Also known as: FA2, FAAP90, FAAP95, FAB, FACB, FANCB
    Summary: Fanconi anemia complementation group B

Clinical features


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