Label
Description
KFPT:PT-FC5N96D8 CUI has phenotype Pierre Robin Syndrome
A Knowledge Graph Assertion from Kids First
KFPT:PT-FC5N96D8 CUI has phenotype Aortic coarctation
KFPT:PT-FC5N96D8 CUI has phenotype Cardiomyopathies
KFPT:PT-FC5N96D8 CUI has phenotype Congenital atresia of rectum
KFPT:PT-FC5N96D8 CUI has phenotype Dextrocardia
KFPT:PT-FC5N96D8 CUI has phenotype Rectoperineal fistula
KFPT:PT-FC5N96D8 CUI has phenotype Abnormality of metabolism/homeostasis
KFPT:PT-FC5N96D8 CUI has phenotype Ventricular Septal Defects
KFPT:PT-FC5N96D8 CUI has phenotype Tetralogy of Fallot
KFPT:PT-FC5N96D8 CUI has phenotype Spinal fusion