Label
Description
KFPT:PT-CCMWKD97 CUI has phenotype Imaging of brain abnormal
A Knowledge Graph Assertion from Kids First
KFPT:PT-CCMWKD97 CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-CCMWKD97 CUI has phenotype Congenital anomaly of face
KFPT:PT-CCMWKD97 CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-CCMWKD97 CUI has phenotype Congenital digestive system anomalies
KFPT:PT-CCMWKD97 CUI has phenotype Facial Paresis
KFPT:PT-CCMWKD97 CUI has phenotype Abnormal palate morphology
KFPT:PT-CCMWKD97 CUI has phenotype Phenotypic abnormality
KFPT:PT-CCMWKD97 CUI has phenotype Urogenital Diseases
KFPT:PT-CCMWKD97 CUI has phenotype Limited extraocular movements