Label
Description
KFPT:PT-9H1PM622 CUI has phenotype Sudden death
A Knowledge Graph Assertion from Kids First
KFPT:PT-9H1PM622 CUI has phenotype Congenital atresia of rectum
KFPT:PT-9H1PM622 CUI has phenotype Congenital anomaly of face
KFPT:PT-9H1PM622 CUI has phenotype Abnormal connection between trachea and esophagus
KFPT:PT-9H1PM622 CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas
KFPT:PT-9H1PM622 CUI has phenotype Rectoperineal fistula
KFPT:PT-9H1PM622 CUI has phenotype Pierre Robin Syndrome
KFPT:PT-9H1PM622 CUI has phenotype Spinal fusion
KFPT:PT-9H1PM622 CUI has phenotype Craniosynostosis
KFPT:PT-9H1PM622 CUI has phenotype Dextrocardia