Label
Description
KFPT:PT-EJ41M5BE CUI has phenotype Urogenital Diseases
A Knowledge Graph Assertion from Kids First
KFPT:PT-EJ41M5BE CUI has phenotype Limited extraocular movements
KFPT:PT-EJ41M5BE CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-EJ41M5BE CUI has phenotype Facial Paresis
KFPT:PT-EJ41M5BE CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-EJ41M5BE CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-EJ41M5BE CUI has phenotype Abnormal palate morphology
KFPT:PT-EJ41M5BE CUI has phenotype Imaging of brain abnormal
KFPT:PT-EJ41M5BE CUI has phenotype Hearing abnormality
KFPT:PT-EJ41M5BE CUI has phenotype Congenital digestive system anomalies