Label
Description
KFPT:PT-1RFJT4B5 CUI has phenotype Abnormal tricuspid valve morphology
A Knowledge Graph Assertion from Kids First
KFPT:PT-1RFJT4B5 CUI has phenotype Abnormal ventriculoarterial connection
KFPT:PT-1RFJT4B5 CUI has phenotype Congenital blindness
KFPT:PT-1RFJT4B5 CUI has phenotype Craniosynostosis
KFPT:PT-1RFJT4B5 CUI has phenotype Abnormality of the hepatic vasculature
KFPT:PT-1RFJT4B5 CUI has phenotype Congenital scar
KFPT:PT-1RFJT4B5 CUI has phenotype Preauricular dimple
KFPT:PT-1RFJT4B5 CUI has phenotype Branchioma
KFPT:PT-1RFJT4B5 CUI belongs to cohort Kids First: Congenital Heart Defects
KFPT:PT-1RFJT4B5 CUI has phenotype Tetralogy of Fallot