Label
Description
KFPT:PT-WRMVZN2Y CUI has phenotype Scoliosis, unspecified
A Knowledge Graph Assertion from Kids First
KFPT:PT-WRMVZN2Y CUI has phenotype Congenital anomaly of face
KFPT:PT-WRMVZN2Y CUI has phenotype Imaging of brain abnormal
KFPT:PT-WRMVZN2Y CUI has phenotype Limited extraocular movements
KFPT:PT-WRMVZN2Y CUI has phenotype Phenotypic abnormality
KFPT:PT-WRMVZN2Y CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-WRMVZN2Y CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-WRMVZN2Y CUI has phenotype Abnormal palate morphology
KFPT:PT-WRMVZN2Y CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-WRMVZN2Y CUI has phenotype Facial Paresis