Label
Description
KFPT:PT-RBA0RK7G CUI belongs to cohort Kids First: Congenital Heart Defects
A Knowledge Graph Assertion from Kids First
KFPT:PT-RBA0RK7G CUI has phenotype Arnold Chiari Malformation
KFPT:PT-RBA0RK7G CUI has phenotype Left Isomerism
KFPT:PT-RBA0RK7G CUI has phenotype Polydactyly of toes
KFPT:PT-RBA0RK7G CUI has phenotype Decreased projection of lower jaw
KFPT:PT-RBA0RK7G CUI has phenotype Syndactyly of fingers
KFPT:PT-RBA0RK7G CUI has phenotype Abnormal ventriculoarterial connection
KFPT:PT-RBA0RK7G CUI has phenotype Abnormal coronary artery morphology
KFPT:PT-RBA0RK7G CUI has phenotype Asplenia Syndrome
KFPT:PT-RBA0RK7G CUI has phenotype Conotruncal defect