Label
Description
KFPT:PT-S3M51MYV CUI has phenotype Limited extraocular movements
A Knowledge Graph Assertion from Kids First
KFPT:PT-S3M51MYV CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-S3M51MYV CUI has phenotype Imaging of brain abnormal
KFPT:PT-S3M51MYV CUI has phenotype Phenotypic abnormality
KFPT:PT-S3M51MYV CUI has phenotype Scoliosis, unspecified
KFPT:PT-S3M51MYV CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-S3M51MYV CUI has phenotype Congenital anomaly of face
KFPT:PT-S3M51MYV CUI has phenotype Facial Paresis
KFPT:PT-S3M51MYV CUI has phenotype Abnormal palate morphology
KFPT:PT-S3M51MYV CUI has phenotype Lower cranial nerve dysfunction