Label
Description
KFPT:PT-FP6X2ECG CUI has phenotype Imaging of brain abnormal
A Knowledge Graph Assertion from Kids First
KFPT:PT-FP6X2ECG CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-FP6X2ECG CUI has phenotype Abnormal palate morphology
KFPT:PT-FP6X2ECG CUI has phenotype Facial Paresis
KFPT:PT-FP6X2ECG CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-FP6X2ECG CUI has phenotype Limited extraocular movements
KFPT:PT-FP6X2ECG CUI has phenotype Congenital anomaly of face
KFPT:PT-FP6X2ECG CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-FP6X2ECG CUI has phenotype Urogenital Diseases
KFPT:PT-FP6X2ECG CUI has phenotype Hearing abnormality