Label
Description
KFPT:PT-NFPXK1ZW CUI has phenotype Abnormal ventriculoarterial connection
A Knowledge Graph Assertion from Kids First
KFPT:PT-NFPXK1ZW CUI has phenotype Congenital blindness
KFPT:PT-NFPXK1ZW CUI has phenotype Abnormal coronary artery morphology
KFPT:PT-NFPXK1ZW CUI has phenotype Preauricular dimple
KFPT:PT-NFPXK1ZW CUI has phenotype Conotruncal defect
KFPT:PT-NFPXK1ZW CUI has phenotype Abnormal mitral valve morphology
KFPT:PT-NFPXK1ZW CUI has phenotype Tetralogy of Fallot
KFPT:PT-NFPXK1ZW CUI has phenotype Retinal vascular tortuosity
KFPT:PT-NFPXK1ZW CUI has phenotype Hypoplastic Left Heart Syndrome
KFPT:PT-NFPXK1ZW CUI has phenotype Craniosynostosis