Label
Description
KFPT:PT-QZT1XVPE CUI has phenotype Congenital digestive system anomalies
A Knowledge Graph Assertion from Kids First
KFPT:PT-QZT1XVPE CUI has phenotype Congenital anomaly of face
KFPT:PT-QZT1XVPE CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-QZT1XVPE CUI has phenotype Facial Paresis
KFPT:PT-QZT1XVPE CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-QZT1XVPE CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-QZT1XVPE CUI has phenotype Hearing abnormality
KFPT:PT-QZT1XVPE CUI has phenotype Urogenital Diseases
KFPT:PT-QZT1XVPE CUI has phenotype Limited extraocular movements
KFPT:PT-QZT1XVPE CUI has phenotype Scoliosis, unspecified