Label
Description
KFPT:PT-NMTZN1ME CUI has phenotype Aortic coarctation
A Knowledge Graph Assertion from Kids First
KFPT:PT-NMTZN1ME CUI has phenotype Congenital anomaly of face
KFPT:PT-NMTZN1ME CUI has phenotype Congenital atresia of rectum
KFPT:PT-NMTZN1ME CUI has phenotype Cardiomyopathies
KFPT:PT-NMTZN1ME CUI has phenotype Megacolon
KFPT:PT-NMTZN1ME CUI belongs to cohort Kids First: Esophageal Atresia and Tracheoesophageal Fistulas
KFPT:PT-NMTZN1ME CUI has phenotype Craniosynostosis
KFPT:PT-NMTZN1ME CUI has phenotype Dextrocardia
KFPT:PT-NMTZN1ME CUI has phenotype Abnormality of metabolism/homeostasis
KFPT:PT-NMTZN1ME CUI has phenotype Hypoplastic Left Heart Syndrome