Label
Description
KFPT:PT-KC00TFXP CUI has phenotype Facial Paresis
A Knowledge Graph Assertion from Kids First
KFPT:PT-KC00TFXP CUI has phenotype Phenotypic abnormality
KFPT:PT-KC00TFXP CUI has phenotype Urogenital Diseases
KFPT:PT-KC00TFXP CUI has phenotype Abnormal palate morphology
KFPT:PT-KC00TFXP CUI has phenotype Imaging of brain abnormal
KFPT:PT-KC00TFXP CUI has phenotype Congenital digestive system anomalies
KFPT:PT-KC00TFXP CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-KC00TFXP CUI has phenotype Limited extraocular movements
KFPT:PT-KC00TFXP CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-KC00TFXP CUI has phenotype Hearing abnormality