Label
Description
KFPT:PT-5NW9Z45D CUI has phenotype Pierre Robin Syndrome
A Knowledge Graph Assertion from Kids First
KFPT:PT-5NW9Z45D CUI has phenotype Cardiomyopathies
KFPT:PT-5NW9Z45D CUI has phenotype Spinal fusion
KFPT:PT-5NW9Z45D CUI has phenotype Congenital anomaly of face
KFPT:PT-5NW9Z45D CUI has phenotype Dextrocardia
KFPT:PT-5NW9Z45D CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas
KFPT:PT-5NW9Z45D CUI has phenotype Ventricular Septal Defects
KFPT:PT-5NW9Z45D CUI has phenotype Sudden death
KFPT:PT-5NW9Z45D CUI has phenotype Rectoperineal fistula
KFPT:PT-5NW9Z45D CUI has phenotype Tetralogy of Fallot