Label
Description
KFPT:PT-F62N403G CUI has phenotype Urogenital Diseases
A Knowledge Graph Assertion from Kids First
KFPT:PT-F62N403G CUI has phenotype Facial Paresis
KFPT:PT-F62N403G CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-F62N403G CUI has phenotype Hearing abnormality
KFPT:PT-F62N403G CUI has phenotype Imaging of brain abnormal
KFPT:PT-F62N403G CUI has phenotype Congenital anomaly of face
KFPT:PT-F62N403G CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-F62N403G CUI has phenotype Phenotypic abnormality
KFPT:PT-F62N403G CUI has phenotype Abnormal palate morphology
KFPT:PT-F62N403G CUI has phenotype Lower cranial nerve dysfunction