Label
Description
KFPT:PT-F4KHQK51 CUI has phenotype Abnormal connection between trachea and esophagus
A Knowledge Graph Assertion from Kids First
KFPT:PT-F4KHQK51 CUI has phenotype Pierre Robin Syndrome
KFPT:PT-F4KHQK51 CUI has phenotype Rectoperineal fistula
KFPT:PT-F4KHQK51 CUI has phenotype Congenital anomaly of face
KFPT:PT-F4KHQK51 CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas
KFPT:PT-F4KHQK51 CUI has phenotype Sudden death
KFPT:PT-F4KHQK51 CUI has phenotype Ventricular Septal Defects
KFPT:PT-F4KHQK51 CUI has phenotype Dextrocardia
KFPT:PT-F4KHQK51 CUI has phenotype Hypoplastic Left Heart Syndrome
KFPT:PT-F4KHQK51 CUI has phenotype Craniosynostosis