Label
Description
KFPT:PT-RDV1F3BE CUI has phenotype Congenital anomaly of face
A Knowledge Graph Assertion from Kids First
KFPT:PT-RDV1F3BE CUI has phenotype Lower cranial nerve dysfunction
KFPT:PT-RDV1F3BE CUI has phenotype Limited extraocular movements
KFPT:PT-RDV1F3BE CUI belongs to cohort Kids First: Syndromic Cranial Dysinnervation
KFPT:PT-RDV1F3BE CUI has phenotype Cardiovascular Abnormalities
KFPT:PT-RDV1F3BE CUI has phenotype Abnormal palate morphology
KFPT:PT-RDV1F3BE CUI has phenotype Phenotypic abnormality
KFPT:PT-RDV1F3BE CUI has phenotype Hearing abnormality
KFPT:PT-RDV1F3BE CUI has phenotype Scoliosis, unspecified
KFPT:PT-RDV1F3BE CUI has phenotype Facial Paresis