Label
Description
KFPT:PT-PHKDXW1V CUI has phenotype Retinal vascular tortuosity
A Knowledge Graph Assertion from Kids First
KFPT:PT-PHKDXW1V CUI belongs to cohort Kids First: Congenital Heart Defects
KFPT:PT-PHKDXW1V CUI has phenotype Tetralogy of Fallot
KFPT:PT-PHKDXW1V CUI has phenotype Abnormal aortic morphology
KFPT:PT-PHKDXW1V CUI has phenotype Abnormal ventriculoarterial connection
KFPT:PT-PHKDXW1V CUI has phenotype Branchioma
KFPT:PT-PHKDXW1V CUI has phenotype Limited eye motility from Duane anomaly
KFPT:PT-PHKDXW1V CUI has phenotype Abnormal mitral valve morphology
KFPT:PT-PHKDXW1V CUI has phenotype Congenital blindness
KFPT:PT-PHKDXW1V CUI has phenotype Preauricular dimple