Label
Description
KFPT:PT-F43APHDJ CUI has phenotype Pierre Robin Syndrome
A Knowledge Graph Assertion from Kids First
KFPT:PT-F43APHDJ CUI has phenotype Hernia, Inguinal
KFPT:PT-F43APHDJ CUI has phenotype Spinal fusion
KFPT:PT-F43APHDJ CUI has phenotype Rectoperineal fistula
KFPT:PT-F43APHDJ CUI has phenotype Ventricular Septal Defects
KFPT:PT-F43APHDJ CUI has phenotype Congenital anomaly of face
KFPT:PT-F43APHDJ CUI has phenotype Abnormal connection between trachea and esophagus
KFPT:PT-F43APHDJ CUI has phenotype Tetralogy of Fallot
KFPT:PT-F43APHDJ CUI has phenotype Abnormality of metabolism/homeostasis
KFPT:PT-F43APHDJ CUI has phenotype Cardiomyopathies