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

Summary

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.

Available tests

25 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: FAAP250, KIAA1596, FANCM
    Summary: Fanconi anemia complementation group M

Practice guidelines

  • FARF, 2008
    Fanconi Anemia Research Fund, Guidelines for Diagnosis and Management, 2008

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