Label
Description
KFPT:PT-C0Z69FZM CUI has phenotype Ventricular Septal Defects
A Knowledge Graph Assertion from Kids First
KFPT:PT-C0Z69FZM CUI has phenotype Pierre Robin Syndrome
KFPT:PT-C0Z69FZM CUI has phenotype Cleft lip
KFPT:PT-C0Z69FZM CUI has phenotype Congenital atresia of rectum
KFPT:PT-C0Z69FZM CUI has phenotype Rectoperineal fistula
KFPT:PT-C0Z69FZM CUI has phenotype Uranostaphyloschisis
KFPT:PT-C0Z69FZM CUI has phenotype Sudden death
KFPT:PT-C0Z69FZM CUI has phenotype Craniosynostosis
KFPT:PT-C0Z69FZM CUI has phenotype Abnormality of metabolism/homeostasis
KFPT:PT-C0Z69FZM CUI has phenotype Hypoplastic Left Heart Syndrome