Label
Description
KFPT:PT-C23RMCVP CUI has phenotype Limited extraocular movements
A Knowledge Graph Assertion from Kids First
KFPT:PT-C23RMCVP CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-C23RMCVP CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-C23RMCVP CUI has phenotype Hearing abnormality
KFPT:PT-C23RMCVP CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-C23RMCVP CUI has phenotype Congenital anomaly of face
KFPT:PT-C23RMCVP CUI has phenotype Congenital digestive system anomalies
KFPT:PT-C23RMCVP CUI has phenotype Facial Paresis
KFPT:PT-C23RMCVP CUI has phenotype Phenotypic abnormality
KFPT:PT-C23RMCVP CUI has phenotype Imaging of brain abnormal