Label
Description
KFPT:PT-NEAM0FX2 CUI has phenotype Microcephaly (physical finding)
A Knowledge Graph Assertion from Kids First
KFPT:PT-NEAM0FX2 CUI has phenotype Congenital blindness
KFPT:PT-NEAM0FX2 CUI has phenotype Craniosynostosis
KFPT:PT-NEAM0FX2 CUI has phenotype Tetralogy of Fallot
KFPT:PT-NEAM0FX2 CUI has phenotype Left ventricular abnormality
KFPT:PT-NEAM0FX2 CUI has phenotype Retinal vascular tortuosity
KFPT:PT-NEAM0FX2 CUI has phenotype Abnormal ventriculoarterial connection
KFPT:PT-NEAM0FX2 CUI has phenotype Abnormal coronary artery morphology
KFPT:PT-NEAM0FX2 CUI has phenotype Branchioma
KFPT:PT-NEAM0FX2 CUI has phenotype Abnormal mitral valve morphology