Label
Description
KFPT:PT-RBPCW99X CUI has phenotype Lower cranial nerve dysfunction
A Knowledge Graph Assertion from Kids First
KFPT:PT-RBPCW99X CUI has phenotype Congenital anomaly of face
KFPT:PT-RBPCW99X CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-RBPCW99X CUI has phenotype Scoliosis, unspecified
KFPT:PT-RBPCW99X CUI has phenotype Limited extraocular movements
KFPT:PT-RBPCW99X CUI has phenotype Abnormal palate morphology
KFPT:PT-RBPCW99X CUI has phenotype Hearing abnormality
KFPT:PT-RBPCW99X CUI has phenotype Imaging of brain abnormal
KFPT:PT-RBPCW99X CUI has phenotype Urogenital Diseases
KFPT:PT-RBPCW99X CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation