Label
Description
KFPT:PT-TTQ9GV49 CUI has phenotype Scoliosis, unspecified
A Knowledge Graph Assertion from Kids First
KFPT:PT-TTQ9GV49 CUI has phenotype Limited extraocular movements
KFPT:PT-TTQ9GV49 CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-TTQ9GV49 CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-TTQ9GV49 CUI has phenotype Urogenital Diseases
KFPT:PT-TTQ9GV49 CUI has phenotype Hearing abnormality
KFPT:PT-TTQ9GV49 CUI has phenotype Phenotypic abnormality
KFPT:PT-TTQ9GV49 CUI has phenotype Imaging of brain abnormal
KFPT:PT-TTQ9GV49 CUI has phenotype Congenital digestive system anomalies
KFPT:PT-TTQ9GV49 CUI has phenotype Congenital anomaly of face