Label
Description
KFPT:PT-PX1N9AWZ CUI has phenotype Congenital blindness
A Knowledge Graph Assertion from Kids First
KFPT:PT-PX1N9AWZ CUI has phenotype Pyloric Stenosis, Hypertrophic
KFPT:PT-PX1N9AWZ CUI belongs to cohort Kids First: Congenital Heart Defects
KFPT:PT-PX1N9AWZ CUI has phenotype Renal dysplasia
KFPT:PT-PX1N9AWZ CUI has phenotype Subglottic stenosis
KFPT:PT-PX1N9AWZ CUI has phenotype Polycystic Kidney - body part
KFPT:PT-PX1N9AWZ CUI has phenotype Wide spaced nipples
KFPT:PT-PX1N9AWZ CUI has phenotype Spinal fusion
KFPT:PT-PX1N9AWZ CUI has phenotype Left ventricular abnormality
KFPT:PT-PX1N9AWZ CUI has phenotype Abnormal mitral valve morphology