Label
Description
KFPT:PT-PBPQA6XT CUI has phenotype Congenital anomaly of face
A Knowledge Graph Assertion from Kids First
KFPT:PT-PBPQA6XT CUI has phenotype Urogenital Diseases
KFPT:PT-PBPQA6XT CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-PBPQA6XT CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-PBPQA6XT CUI has phenotype Imaging of brain abnormal
KFPT:PT-PBPQA6XT CUI has phenotype Scoliosis, unspecified
KFPT:PT-PBPQA6XT CUI has phenotype Congenital digestive system anomalies
KFPT:PT-PBPQA6XT CUI has phenotype Limited extraocular movements
KFPT:PT-PBPQA6XT CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-PBPQA6XT CUI has phenotype Abnormal palate morphology