Label
Description
KFPT:PT-KVRPX50M CUI has phenotype Urogenital Diseases
A Knowledge Graph Assertion from Kids First
KFPT:PT-KVRPX50M CUI has phenotype Facial Paresis
KFPT:PT-KVRPX50M CUI has phenotype Phenotypic abnormality
KFPT:PT-KVRPX50M CUI has phenotype Congenital anomaly of face
KFPT:PT-KVRPX50M CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-KVRPX50M CUI has phenotype Limited extraocular movements
KFPT:PT-KVRPX50M CUI has phenotype Abnormal palate morphology
KFPT:PT-KVRPX50M CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-KVRPX50M CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-KVRPX50M CUI has phenotype Imaging of brain abnormal