Label
Description
KFPT:PT-T8YKNXD4 CUI has phenotype Abnormal connection between trachea and esophagus
A Knowledge Graph Assertion from Kids First
KFPT:PT-T8YKNXD4 CUI has phenotype Wolff-Parkinson-White Syndrome
KFPT:PT-T8YKNXD4 CUI has phenotype Cardiomyopathies
KFPT:PT-T8YKNXD4 CUI has phenotype Congenital atresia of rectum
KFPT:PT-T8YKNXD4 CUI has phenotype Pierre Robin Syndrome
KFPT:PT-T8YKNXD4 CUI has phenotype Tetralogy of Fallot
KFPT:PT-T8YKNXD4 CUI has phenotype Cleft lip
KFPT:PT-T8YKNXD4 CUI has phenotype Hypoplastic Left Heart Syndrome
KFPT:PT-T8YKNXD4 CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas
KFPT:PT-T8YKNXD4 CUI has phenotype Congenital anomaly of face