Label
Description
KFPT:PT-D5MWCY68 CUI has phenotype Congenital anomaly of face
A Knowledge Graph Assertion from Kids First
KFPT:PT-D5MWCY68 CUI has phenotype Tetralogy of Fallot
KFPT:PT-D5MWCY68 CUI has phenotype Ventricular Septal Defects
KFPT:PT-D5MWCY68 CUI has phenotype Hypoplastic Left Heart Syndrome
KFPT:PT-D5MWCY68 CUI has phenotype Cleft lip
KFPT:PT-D5MWCY68 CUI has phenotype Uranostaphyloschisis
KFPT:PT-D5MWCY68 CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas
KFPT:PT-D5MWCY68 CUI has phenotype Pierre Robin Syndrome
KFPT:PT-D5MWCY68 CUI has phenotype Abnormality of metabolism/homeostasis
KFPT:PT-D5MWCY68 CUI has phenotype Abnormal connection between trachea and esophagus